Basic Information, Form No. 1

Basic Information, Form No.
For
Amendment in existing Environmental

Clearance for mode of disposal of
Effluent stream
Submitted by
M/s. Aether Industries Ltd.

Plot No. 8203, Sachin GIDC,
Surat, Gujarat
FORM 1
(I) Basic Information
Sr.
Item Details
No.
M/s. Aether Industries Limited

1. Name of the projects Plot No. 8203, Road Number 82, Sachin
GIDC, Surat, Gujarat
5(f) – Synthetic Organic Chemicals
2. S. No. in the schedule
Category - B
3. Proposed capacity/area/length/tonnage to Aether Industries Limited has valid
be handled/command area/lease (CC&A) vide order no. AWH-88433 issued
area/number of wells to be drilled. on dated 21/09/2017 valid up to
06/04/2022.
The proposed Amendment is for change

in mode of disposal of waste water and
replacement of some existing products.
Proposed Amendment:
Stream ‘B’ – 90 KLD effluent; treated in

existing facility of primary and phantom
treatment followed by RO plant will be
now segregated into two parts.
i)15 KLD effluent generated from group
‘E’ products will be sent to common MEE
facility of Globe Enviro Care Limited
(GECL)
ii)Rest 75 KLD effluent will continue to be
treated as per existing treatment scheme.
There will be replacement of some

existing products with new products.
However, total production capacity of the
plant will remain same. Pollution load
comparison of new products with existing
products to be replaced are provided in
Annexure III
4. New/Expansion/Modernization Case is for EC Amendment.
Existing production capacity as granted in
EC and CCA is 475 MT/Month and it will
remain same after proposed EC
Amendment.
5. Existing Capacity/Area etc.
Total area of the plot is 10500 sq.m.

There will be no change in existing plant
layout.
6. Category of Project i.e. ‘A’ or ‘B’ “B’’ (Plant is in notified GIDC-Sachin)
Does it attract the general condition? If
7. Not applicable
yes, please specify.
Does it attract the specific condition? If Not applicable
8.
yes, please specify.
9. Location
Plot/Survey/Khasra No. Plot No. 8203
Village Sachin
Tehsil Chorasi
District Surat
State Gujarat
Nearest railway station/airport along with Sachin Railway station: 2.75 Km Aerial
10.
distance in kms. Surat airport: 12 Km Aerial
Nearest Town, city, District Headquarters
11. Sachin: 3 Km
along with distance in kms.
Village Panchayats, Zilla Parishad,
Municipal Corporation, Local body
12. G.I.D.C. Sachin
(complete postal addresses with telephone
nos. to be given)
13. Name of the applicant Mr. Ashvin Desai
Plot No. 8203, G.I.D.C, Sachin, Surat-
14. Registered Address
394230
15. Address for correspondence :
Name Mr. Ashvin Desai
Designation (Owner/Partner/CEO) Director
Plot No. 8203, G.I.D.C, Sachin, Surat-
Address
394230
Pin Code 394230
E-mail ashvin@aether.co.in
Telephone No. 0261- 3303000
Fax No. 0261- 3303000
16. Details of Alternative Sites examined, if Not applicable
any. Location of these sites should be
shown on a topo sheet
17. Interlinked Projects Not applicable
Whether separate application of interlinked
18. Not applicable
project has been submitted?
19. If yes, date of submission Not applicable
20. If no, reason Not applicable
Whether the proposal involves
21. approval/clearance under: if yes, details of
the same and their status to be given.
Not applicable
(a) The Forest (Conservation) Act, 1980?
(b) The Wildlife (Protection) Act, 1972?
(c) The C.R.Z Notification, 1991?
Whether there is any Government
22. Not applicable
Order/Policy relevant/relating to the site?
23. Forest land involved (hectares) Not applicable
Whether there is any litigation pending
24. against the project and/or land in which
the project is propose to be set up?
(a) Name of the Court No litigation pending against the project
(b) Case No. and/ or land.
(c) Orders/directions of the Court, if any
and its relevance with the proposed
project.
Existing: 59.99 Crore
25. Project cost (Rs. In lacs)
Proposed additional: 2.00 Crore
(II) Activity
1. Construction, operation or decommissioning of the Project involving actions,

which will cause physical changes in the locality (topography, land use, changes
in water bodies, etc.)
Details thereof (with approximate

Sr. Information / Checklist Yes/
quantities / rates, wherever possible)
No. Confirmation No
with source of information data
Permanent or temporary change

in land use, land cover or No change in land use, land cover or
topography as amendment is only for change
1.1 topography including increase in NO
in mode of disposal of effluent and changes in
intensity of land use (with few products. Existing plot is within notified
respect to local land use plan) I/A of Sachin GIDC.
Clearance of existing land,

1.2 NO
vegetation and buildings? Not Applicable
1.3 Creation of new land uses? NO Not applicable
Pre-construction investigations
1.4 NO Not applicable
e.g. bore houses, soil testing?
1.5 Construction works? NO Not applicable
1.6 Demolition works? NO Not applicable
Temporary sites used for

1.7 construction works or housing of NO Not applicable. No construction activities will
construction workers? be carried out for proposed amendment.
Above ground buildings,

structures or earthworks
including linear structures, cut
and fill or excavations
Underground works including

mining or tunnelling?
1.10 Reclamation works? NO Not applicable

1.11 Dredging? NO Not applicable
1.12 Offshore structures? NO Not applicable
Production capacity will remain same.

However, some products will be removed and
Production and manufacturing few new products are proposed to be added
1.13 YES
processes? without increasing production capacity.
More details are provided, please refer
Annexure III
Facilities for storage of goods or No change in storage facility. Existing facilities
1.14 YES
materials? will be use.
For details of solid / hazardous waste

generation and disposal please refer
Annexure V
Facilities for treatment or There are no changes in quantity of

1.15 disposal of solid waste or liquid YES wastewater generation. Only quantity of WW
effluents? generated from stream-B will be segregated
into two parts and its disposal method is
proposed to change. More details comparing
existing facility and proposed facility are
mentioned in Annexure IV
Facilities for long term housing

of operational workers?
The existing infrastructure and transportation

New road, rail or sea traffic system in GIDC-Sachin is adequate and
1.17 NO
during construction or operation? connects the unit with highway and railway
station.
New road, rail, air, waterborne

or other transport infrastructure
including new or altered routes
and stations, ports, airports etc.?
Closure or diversion of existing

transport routes or infrastructure
leading to changes in traffic
movements?
1.20 New or diverted transmission NO Not applicable

lines or pipelines?
Impoundment, damming,
culverting, realignment or other
changes to the hydrology of
watercourses or aquifers?
1.22 Stream crossings? NO Not applicable
No ground water is being utilize for any of the

Abstraction or transfers of water activity.
1.23 NO
from ground or surface waters? The source of water supply is from Sachin
GIDC.
Changes in water bodies or the Proper storm water discharge is installed.

1.24 land surface affecting drainage NO
or run-off? No changes due to proposed amendment.
Transport of personnel or
The unit is located within Sachin GIDC having
1.25 materials for construction, NO
adequate transportation system.
operation or decommissioning?
Long-term dismantling or
1.26 decommissioning or restoration NO Not applicable
works?
Ongoing activity during

decommissioning which could
have an impact on the
environment?
Influx of people to an area in

1.28 either temporarily or NO
Not applicable
permanently?
1.29 Introduction of alien species? NO Not applicable
Loss of native species or genetic

diversity?
1.31 Any other actions? NO Not applicable

2. Use of Natural resources for construction or operation of the Project (such as
land, water, materials or energy, especially any resources which are non-
renewable or in short supply)
Sr. Information / Checklist Yes/ Details thereof (with approximate

No. Confirmation No quantities / rates, wherever possible)
2.1 Land especially undeveloped or NO Activity shall be carried out within existing
agricultural land (ha) premises only.
2.2 Water (expected source & YES The water requirement of this project is 364
competing users) unit : KLD KLD and will meet by Sachin Notified Area
Authority. Refer Annexure-IV for details.
2.3 Minerals (MT) NO Not applicable
2.4 Construction material - stone, NO Not applicable
aggregates, sand / soil (expected
source - MT)
2.5 Forests and timber NO Not applicable
(source - MT)
2.6 Energy including electricity and The power requirement of the project is 2000
fuels (source, competing users) KVA which is sourced by Torrent Energy Ltd.
NO
Unit : fuel (MT), energy (MW) 2 no. of D.G. set is available for emergency
power backup.
2.7 Any other natural resources (use NO Nil
appropriate standard units)
3. Use, storage, transport, handling or production of substances or materials, which
could be harmful to human health or the environment or raise concerns about actual
or perceived risks to human health.
S. No. Information / Checklist Yes Details thereof (with approximate

Confirmation / No quantities / rates, wherever possible) with
source of information data
3.1 Use of substances or materials, YES For detail please refer Annexure V
which are hazardous (as per
MSIHC rules) to human health
or the environment (flora,
fauna, and water supplies)
3.2 Changes in occurrence of NO None

disease or affect disease
vectors (e.g. insect or water
borne diseases)
3.3 Affect the welfare of people NO Not applicable. However, due to amendment
e.g. by changing living there will be employment generation for
conditions? transportation of waste water from premises to
common facility.
3.4 Vulnerable groups of people NO Not applicable

who could be affected by the
project e.g. hospital patients,
children, the elderly etc.
3.5 Any other causes NO NIL

4. Production of solid wastes during construction or operation or decommissioning
(MT/month)
Sr. Information / Checklist Yes Details thereof (with approximate

No. Confirmation / No quantities / rates, wherever possible)
4.1 Spoil, overburden or mine NO NIL

wastes
4.2 Municipal waste (domestic and / YES Domestic waste will be disposed off through
or commercial wastes) septic tank/soak pit system.
For detail please refer Annexure V
4.3 Hazardous wastes (as per YES For detail please refer Annexure V
Hazardous Waste Management
Rules)
4.4 Other industrial process wastes YES For detail please refer Annexure V
4.5 Surplus product NO Not applicable.
4.6 Sewage sludge or other sludge YES Details are provided in Annexure V
from effluent treatment
4.7 Construction or demolition NO Not applicable. No additional construction will be

wastes carried out for proposed amendment.
4.8 Redundant machinery or NO Not applicable

equipment
4.9 Contaminated soils or other NO Not applicable

materials
However, incase of leakage of wastewater, its
management plant provided in EIA and earlier
EC will be followed.
4.10 Agricultural wastes NO NIL
4.11 Other solid wastes NO NIL

5. Release of pollutants or any hazardous, toxic or noxious substances to air (Kg/hr)
Sr.No. Information Details thereof (with approximate

/ Checklist Yes/
Confirmation No
Emissions from combustion of fossil

5.1 fuels from stationary or mobile NO For details please refer Annexure VI
sources
For detail please refer in Annexure VI
5.2 Emissions from production processes YES However, due to proposed amendment,
there will be no increase in emissions from
production activities.
There shall be fugitive emissions during

Emissions from materials handling
5.3 YES handling of raw materials, which is
including storage or transport controlled by good engineering practices
and same shall be followed in future.
Emissions from construction
5.4 activities including plant and NO Not applicable
equipment
Dust or odors from handling of

5.5 materials including construction NO Not applicable
materials, sewage and waste
5.6 Emissions from incineration of waste NO No such activity is proposed
Emissions from burning of waste in

5.7 open air (e.g. slash materials, NO No such activity is proposed
construction debris)
5.8 Emissions from any other sources NO NIL

6. Generation of Noise and Vibration, and Emissions of Light and Heat
Sr. Details thereof (with approximate

No. Information / Checklist Yes/
Confirmation No
The noise levels near the sources such as D.

G. Set, Boiler etc. will be higher during the
From operation of equipment e.g. operational phase. However, noise levels
6.1 YES within plant remain below 75 dB(A).
engines, ventilation plant, crushers
Due to proposed amendment there will be no
such additional effect in existing noise level.
From industrial or similar All machinery / equipment is having barriers /

6.2 YES enclosures such that noise level remains
processes
within permissible limits.
6.3 From construction or demolition NO Not applicable
6.4 From blasting or piling NO Not applicable
From construction or operational

traffic
6.6 From lighting or cooling systems NO Not applicable
6.7 From any other sources NO Not applicable

7. Risks of contamination of land or water from releases of pollutants into the
ground or into sewers, surface waters, groundwater, coastal waters or the sea
Sr. Details thereof (with approximate

No. Information / Checklist Yes/
Confirmation No
The raw material storage area is having a

From handling, storage, use or pucca floor with impervious layer so as to
7.1 NO
spillage of hazardous materials avoid any contamination due to spillage of
hazardous chemicals / materials.
From discharge of sewage or other
effluents to water or the land
(expected mode and place of
discharge)
By deposition of pollutants emitted

to air, into the land or into water
7.4 From any other sources NO Not applicable
Is there a risk of long term build up

7.5 of pollutants in the environment NO Not applicable
from these sources?
8. Risk of accidents during construction or operation of the Project, which could
affect human health or the environment
Sr. Information / Checklist Yes Details thereof (with approximate

No. Confirmation /No quantities / rates, wherever
possible) with source of information
data
8.1 From explosions, spillages, fires etc. YES Company uses some explosive chemicals
from storage, handling, use or during manufacturing activities. However,
production of hazardous substances proper handling is being followed. Safety
procedures are being followed under
safety supervisor and same will continue
to be followed.
8.2 From any other causes NO Not applicable
8.3 Could the project be affected by YES Project site is located in seismic Zone- III.
natural disasters causing Existing construction is done considering
environmental damage (e.g. floods, same.
earthquakes, landslides, cloudburst
etc)?
9. Factors which should be considered (such as consequential development) which

could lead to environmental effects or the potential for cumulative impacts with
other existing or planned activities in the locality
S. Information / Checklist Yes/ Details thereof (with approximate

No. Confirmation No quantities / rates, wherever possible)
9.1 Lead to development of supporting

cities, ancillary development or NO Not applicable
development stimulated by the
project which could have impact on
the environment e.g. :
• Supporting infrastructure (roads,
power supply, waste or waste
water treatment, etc.)
• housing development
• extractive industries
• supply industries
• other
9.2 Lead to after-use of the site, which NO Not applicable
could have an impact on the
environment
9.3 Set a precedent for later NO Not applicable
developments
9.4 Have cumulative effects due to NO Not applicable
proximity to other existing or planned
projects with similar effects
(III) Environmental Sensitivity
Sr. Areas Name /Aerial Distance (within 15 km) from

No. Identity Proposed Project Location Boundary
1. Areas protected under international NO Not applicable

conventions, national or local
legislation for their ecological,
landscape, cultural or other related
value
2. Areas which are important or NO Not applicable

sensitive for ecological reasons -
Wetlands, watercourses or other
water bodies, coastal zone,
biospheres, mountains, forests
3. Areas used by protected, important NO No protected area or sensitive species

or sensitive species of flora or fauna
for breeding, nesting, foraging, within 10 km from the project site.
resting, over wintering, migration
4. Inland, coastal, marine or NO Not applicable

underground waters
5. State, National boundaries NO Not applicable
6. Routes or facilities used by the NO Not applicable

public for access to recreation or
other tourist, pilgrim areas
7. Defence installations NO Not applicable
8. Densely populated or built-up area YES Sachin is @ 3 Km away from the GIDC
estate.
9. Areas occupied by sensitive man- NO Not applicable

made land uses (hospitals, schools,
places of worship, community
facilities)
10. Areas containing important, high NO Not applicable

quality or scarce resources (ground
water resources, surface resources,
forestry, agriculture, fisheries,
tourism, minerals)
11. Areas already subjected to pollution NO Not applicable

or environmental damage (those
where existing legal environmental
standards are exceeded)
12. Areas susceptible to natural hazard NO Not applicable

which could cause the project to
present environmental problems
(earthquakes, subsidence,
landslides, erosion, flooding or
extreme or adverse climatic
conditions)
I hereby given undertaking that the data and information given in the application
and enclosure are true to the best of my knowledge and belief and I am aware that
if any part of the data and information submitted is found to be false or misleading
at any stage, the project will be rejected and clearance give, if any to the project
will be revoked at our risk and cost.
Date: 07/05/2019
Place: Surat
NOTE:
The projects involving clearance under Coastal Regulation Zone Notification, 1991 shall submit
with the application, a C.R.Z. map duly demarcated by one of the authorized agencies, showing
the project activities, w.r.t. C.R.Z (at the stage of TOR) and the recommendations of the State
coastal zone Management Authority (at the stage of EC). Simultaneous action shall also be
taken to obtain the requisite clearance under the provisions of the C.R.Z. Notification, 1991 for
the activities to be located in the CRZ.
The projects to be located within 10 km of the National parks, sanctuaries, Biosphere Reserves,
Migratory corridors of wild Animals, the project proponent shall submit the map duly
authenticated showing by chief wildlife warden showing these features vis-a-vis the project
location and the Recommendation or comments of the Chief Wildlife Warden 'thereon (at the
stage of EC)."
All correspondence with the Ministry of Environment & Forests including submission of
application for TOR/Environment Clearances, subsequent Clarifications, as may be required
from time to time, participation in the EAC Meeting on behalf of the project proponent shall be
made by the authorized signatory only. The authorized signatory should also submit a
document in support of his claim of being an authorized signatory for the specific project.
LIST OF ANNEXURE
Annexure 1 Copy of EC
Annexure 2 Product Profile (existing and proposed)
Annexure 3 Manufacturing Process of new products and
comparison of mass balance with existing products
Annexure 4 Details on Effluent Treatment
Annexure 5 Details of Solid / Hazardous Waste Management
System
Annexure 6 Details on Air Pollution
ANNEXURE – I
COPY OF EC
ANNEXURE - II
EXISTING PRODUCT LIST AND PROPOSED

MODIFICATIONS
PRODUCT NAME AND CAPACITY AS PER GRANTED CC & A
Group Capacity as
Product Name
No. per CC&A
A Research & Development (R & D) Centre along with Pilot 10 MT/Month
Plant and Crams Products
Note:-
Chemistry Competencies (Group/Molecule)
 Hydrogenation/ asymmetric hydrogenation
 Chiral chemistry
 Organometallic chemistry (Grignard, organolithiation)
 Coupling reactions (Suzuki-Miyaura, Heck)
 Photochemistry
 Homogeneous catalysis
 Heterogeneous catalysis
 Exothermic chemistry (azide chemistry, ozonalysis) and
others
B Active Pharmaceuticals Intermediates 25
C Hydrogenation Derivatives 70
D Halogenation Derivatives 20
E Eatherification 75
F Specialty Chemicals (Electronic Chemicals, Fragrance & 40
Flavors and Specialty Monomers and Polymers)
G Heterocyclic Derivatives / Polycyclic Derivatives 40
H Oxidation Derivatives 40
I Carboxylic Acid Derivatives 30
J Basic Aromatic Intermediates 20
K Chiral Resolution Derivatives 10
L Ethylene Oxide an Isobutylene Intermediastes 75
M Organomettalic Chemistry Derivatives (Grignard, Lithiation, 20
Coupling)
Total 475
The detailed Product list for other groups are given below further to this
table
DETAILED PRODUCT LIST: (EXISTING PRODUCT LIST WITH REMARKS)
Production Remarks
Group
Product Name (MT/Mont
No.
h)
Group B Active Pharmaceuticals Intermediates 25 No changes

MEP Derivatives
1 1-(4-(2-methoxyethyl)phenoxy)propan-2-ol
(RS)-1-(Isopropylamino)-3-[4-
2
(methoxyethyl)phenoxy]propan-2-ol
(±)-1-(Isopropylamino)-3-[p-(2-methoxyethyl)phenoxy]-
3
2-propanol succinate
4
2-propanol L-(+)-tartrate
(S)-1-(isopropylamino)-3-(4-(2-
5
methoxyethyl)phenoxy)propan-2-ol
Citalopram Series
S-(+)-4-(4-(dimethylamino)-1-(4-fluorophenyl)-1-
6
hydroxybutyl)-3-(hydroxymethyl)benzonitrile
1-[3-Dimethylamino)propyl]-1-(4-flurophenyl)-1,3-
7
dihydro-5-isobenzofurancarbonitrile hydrobromide
S-(+)-1-[3-dimethylamino)propyl]-1-(4-fluorophenyl)-
8
1,3-dihydro-5-isobenzofurancarbonitrile oxalate
Metoprolol Derivatives
1-(4-((2-isopropoxyethoxy)methyl)phenoxy)-3-
9
(isopropylamino)propan-2-ol
Etodolac Derivatives
10 Etodolac
Atovaquone Derivatives
2-(4-(4-chlorophenyl)cyclohexyl)-3-hydroxynaphthalene-
11
1,4-dione
Mesalamine Derivatives
12 5-Aminosalicylic acid
Group C Hydrogenation Derivatives 70 No changes in

Secondary amine Derivatives production
capacity.
1 (2R, 3R, 4R, 5S)-6-(octylamino)hexane-1,2,3,4,5-pentaol
Product
(2R, 3R, 4R, 5S)-6-(Methylamino)hexane-1,2,3,4,5- number 9 and
2
pentaol 10 are
(2R, 3R, 4R, 5S)-6-(ethylamino)hexane-1,2,3,4,5- proposed to
3
pentaol be replace.
Piperidine Derivatives
4 4-Piperidine Carboxylic Acid
5 4-Piperidine Carboxamide
6 2-aminomethylpiperidine
7 2-Piperidineethanol
Benzhydrol Derivatives
8 a,a-Diphenyl-4-piperidinemethanol
9 Diphenylmethanol
10 4-Chlorobenzhydrol
Cyclohexyl Derivatives
11 1,3-Cyclohexanedione
12 Trans-4-Isopropylcyclohexanecarboxylic acid
13 Trans-4-Amino cyclohexanol
14 Ethyl 4-oxocyclohexanecarboxylate
Benzylamine Derivatives
15 3-Amino Benzylamine
16 2-Chloro Benzylamine
Chiral Amine Derivatives
(S)-2-chloro-N-(2-ethyl-6-methylphenyl)-N-(1-
17
methoxypropan-2-yl)acetamide
Benzenebutanoic acid, β-[[(1,1-
18 dimethylethoxy)Carbonyl]amino]-2,4,5-trifluro-,ethyl
ester,(βR)
19 (R)-1-(naphthalen-1-yl)ethanamine
Chiral Alcohol Derivatives
20 (R)-1-(3,5-bis(trifluoromethyl)phenyl)ethanol
21 3-(dimethylamino)-1-(thiophen-2-yl)propane-1-one
Benzyl Alcohol Derivatives
22 4-(2-amino-1hydroxyethyl)phenol
23 3-(hydroxymethyl)phenol
24 3-Phenoxy Benzyl Alcohol
Amine Arene Derivatives
25 2-Ethyl aniline
27 3-Aminosalicylic Acid
28 Methyl-2-aminobenzoate
30 N-(4-Amino-2,5-dimethylphenyl)acetamide
31 N-(4-Amino-5-chloro-2-methylphenyl)acetamide
32 4'-chloro-[1,1'-biphenyl]-2-amine
33 3- Amino-4-toluic acid
34 2,5-Dimethyl-1,4-phenylenediamine
35 2-Chloro-5-methyl-1,4-phenylenediamine
36 3,3'-Diamino-4,4'-dihydroxydiphenyl sulfone
Alkyl Derivatives
37 N',N'-di-tert-butylethane-1,2-diamine
38 N',N'-dimethylethane-1,2-diamine
Group No Changes
Halogenation Derivatives 20
D
Benzylbromide Derivatives
1 1-(bromomethyl)-4-(trifluoromethoxy)benzene
2 4'-(bromomethyl)-[1,1'-biphenyl]-2-carbonitrile
(S)-2-Chloropropionic Acid / Esters Derivatives
3 2-Chloropropionic acid, ethyl ester
4 2-Chloropropionic acid, methyl ester
Halogenated Aryl Derivatives
5 3-(bromomethyl)pyridine
6 4-(chloromethyl)pyridine
7 4-Bromo-2,6-diisopropylaniline
8 2-bromophenol
9 3-chloro-2,6-diethylaniline
Naphthoquinone Derivatives
10 2-chloronaphthalene-1,4-dione
11 2,3-Dichloro-1,4-Naphthoquinone
Group No Changes
Etherification 75
E with
(S)-2-Chloropropionic Acid / Esters Derivatives production
1 capacity.
(R)-2-(4-Hydroxyphenoxy) propionic acid
(R)-2-(Aryloxy)propionic Acid, Esters derivatives
2 (R)-2-(4-Hydroxyphenoxy)propionic acid, methyl ester Partial
3 (R)-2-(4-Hydroxyphenoxy)propionic acid, ethyl ester Effluent
4 Methyl-(R)-2-{4(2,4- generated
dichlorophenoxy)phenoxy}propaonate from this
group will be
5 Propynyl-(R)-2-[4-[(5-chloro-3-fluoro-2-pyridinyl)oxy]
now sent to
phenoxy] propanoate
common MEE
6 Butyl-(R)-2-(4-((5-(Trifluoromethyl)Pyridin-2- facility of
YL)Oxy)Phenoxy) Propanoate ‘GECL CETP’
7 Methyl-(R)-2-{4-[3-chloro-5-(trifluoromethyl)-2- as new
pyridyloxy]propanoate facility
8 Ethyl (R)-2-[4-(6-chloroquinoxalin-2- Stored.
yloxy)phenoxy]propanoate
9 Ethyl-(R)-2-[4-{6-chloro-2-
benzoxazolyloxy}phenoxy]propanoate
10 Butyl-(R)-2-[4-(4-Cyano-2-Fluorophenoxy)
Phenoxy]Propanoate
Aryl ether Derivatives
11 2-(3-Phenoxyphenyl)propionic acid
12 2-(2-Methoxyphenoxy)ethylamine
13 4-Phenoxy-2, 6-diisopropyl aniline
14 4-Methoxy-3-[3-(4-morpholinyl)propoxy)benzonitrile
15 4-Fluoro-3-phenoxybenzaldehyde
16 2,6-Diisopropyl-4-phenoxyphenylthiourea
17 1-Tert-butyl-3-(2,6-Diisopropyl-4-
phenoxyphenyl)thiourea
18 2,6-Diisopropyl-4-phenoxy phenyl isothiocyanate
Specialty Chemicals (Electronic Chemicals, 40 No changes

Group F Fragrance & Flavors and Specialty Monomers and with
Polymers) production
Cyclohexanone Derivatives capacity.
1 4-Propyl Cyclohezanone
Product no.
2 4-(4'-propylcyclohexyl)phenol
10 and 12 are
(Cyclohexyl)Phenyl Derivatives proposed to
3 Trans-(4'-propylcyclohexyl) cyclohexanone be replaced.
4 4-(Trans-4-propylcyclohexyl) benzoic acid
5 (4-Trans-4-propylcyclohexyl) phenyl boronic acid
Cyclohexyl aryl Derivatives
6 4-(4-chlorophenyl) cyclohexanecarboxylic acid
OLED Derivatives
7 4 - Vinylphenylboronic Acid
8 B-[10-(2-naphthalenyl)-9-anthracenyl] boronic acid
9 4-(naphthalene-2-yl) boronic acid
Fragrance & Flavors
10 1-methoxy-4-(prop-1-en-1-yl) benzene
11 3-(4-Methoxyphenyl)-2-Metylpropanal
12 3-(4-(Tert-butyl)phenyl)-2-methylpropanal
Specialty Monomers and Polymers
13 Tetrahydro-2H-pyran-2-one
14 5-(1H-benzo[d]imidazol-2-yl)pentan-1-amine
15 2-methyl-1,2-oxaphospholan-5-one 2-oxide
16 Boron trichloride-N,N-dimethyloctylamine
Group 40 No changes
Heterocyclic Derivatives / Polycyclic Derivatives
G
Anthraquinone Derivatives
1 1,4-Dihydroxyanthraquinone
2 2,3-dihydro-9,10-dihydroxy-1,4-anthracenedione
Indole Derivatives
3 7-Ethyl Tryptophol
4 Methyl indol-6-carboxylate
5 Indoline
Phthalic acid Derivatives
6 5-nitro isophthalic acid
7 5 carboxyphthalide
Furan Derivatives
8 2,3-dihydro furan
9 2,5-Dihydrofuran
Imidazole Derivatives
10 1- methyl-1H-imidazole
11 2-Butyl-4-Chloro-5-Formylimidazole
Thiophene Derivatives
12 2-(thiophen-2-yl)ethanamine
13 2-(thiophen-2-yl)ethanol
Quinazoline Derivatives
14 4-(4-(tert-butyl)phenethoxy)quinazoline
Tetrahydrofuran Derivatives
15 1[(2S)-tetrahydro-2-furanyl]-ethanone
Pyridine Derivatives
16 4-pyridinecarboxylic acid
17 4-pyridinecarboxamide
18 4-pyridinemethylamine
19 2-(Pyridin-2-yl)ethanol
Pyran Derivatives
20 3,4-Dihydro-2H-pyran
Carbonate Derivatives
Bis (2,5-dioxopyrrolidin-1-yl)carbonate,[N,N-
21
discuccinimidyl carbonate]
Piperazine Derivatives
22 1-(2,3-dichlorophenyl)piperazine hydrochloride
Thiazole Derivatives
23 Thiazol-5-ylmethanol
Diphenyl Methane Derivatives
1,1'-(methylenebis(4,1-phenylene))bis(1H-pyrrole-2,5-
24
dione)
Pyrimidine Derivatives
2-(2,2-Difluoroethoxy)-N-(5,8-
25 dimethoxy[1,2,4]triazol[1,5,7] pyrimidine-2-yl)-6-
(trifluoromethyl)benzenesulfonamide
Sulfamide Derivatives
26 Sulfamide
Group 40 No changes in
Oxidation Derivatives
H production
Aryl Aldehyde Derivatives capacity.
1 4-hydroxy benzaldehyde (PHB)
Product no. 6
2 4-methoxy benzaldehyde / p-anesaldehyde (PAA) and 9 are
3 4-pyridinecarboxaldehyde proposed to be
4 2,6-dichlorobenzaldehyde replaced.
5 3-pyridinecarboxaldehyde
6 4-(diethylamino)-2-hydroxy benzaldehyde
7 2-amino-3,5-dibromobenzaldehyde
Aryl Carboxylic Acid Derivatives
8 4-(tert-butyl)benzoic acid
9 2-Nitro Benzoic acid
10 2,4-Dichlorobenzoic acid
11 3,5-di-t-butyl-4-hydroxy benzoic acid
12 3-methoxy-2-methylbenzoic acid
13 2-ethoxy benzoic acid
14 3-amino-4-methylbenzoic acid
15 Mafenamic acid
16 4-aminobenzoic acid
Keto Aryl Derivatives
17 Naphthalene-1,4-dione
Pyromelllitic Anhydride (benzo(1,2-c;4,5-c')difuran-
18
1,3,5,7-tetraone
Group I Carboxylic Acid Derivatives 30 No Changes in

Benzonitrile Derivatives production
capacity.
1 2-Hydroxy benzonitrile
2 4-Hydroxy benzonitrile Product no 1
3 5-Cyano-3H-isobenzofuranone and 3 are
4 4-chlorobenzonitrile proposed to be
replaced.
5 2-amino-4-chloro benzonitrile
6 2,6-dichlorobenzonitrile
7 4 - chlorophenyl benzene butane nitrile
Aryl Carboxylic Acid Ester Derivatives
8 Methyl 2-nitro Benzoate
10 Methyl 4-amino Benzoate
11 tert-Butyl 4-(chloromethyl)benzoate
12 Dimethyl-5-aminoisophthalate
13 Methyl-3-amino-4-toluate
14 Ethyl paraben
15 Propyl paraben
16 Ethyl-4 amino benzoate
17 4'-methyl-2-biphenyl carboxylic acid methyl ester
18 Hexyl-3,5-di-tert-butyl-4-hydroxybenzoate
Aryl Acetyl Derivatives
19 N-(2,5-Dimethylphenyl)acetamide
20 N-(5-Chloro-2-methylphenyl)acetamide
21 3-Nitrophenyl acetate
22 2-Acetylthiophene
Aryl Acid chloride Derivatives
23 3-methoxy-2methyl benzoyl chloride
Benzamide Derivatives
24 2-Chloro-n-(4'-chloro-[1,1'-biphenyl]-2-yl)nicotinamide
25 4-chloro-2nitro benzamide
Group J Basic Aromatic Intermediates 20 No Changes in

Aryl Hydrazine Derivatives production
capacity.
1 2 - Ethyl Phenyl Hydrazine Hydrochloride
2 p-Sulphonamide phenyl hydrazine hydrochloride Product no. 12
Nitroarene Derivatives and 13 are
3 2-Cholro - 5-nitro benzoic acid proposed to be
replaced.
4 3-Nitro 2-Cholro benzoic acid
5 N - (2,5- Dimethyl-4-nitophenyl) acetamide
6 N - (5-Chloro-4-nitro-2-methylphenyl) acetamide
7 3-Nitro -4-toluic acid
8 2-Nitro-3-chlorobanzoic acid
10 5 - Nitovanillin
11 3,3'-Diamino-4, 4' - dihydroxydiphenylsulfone
Hydroxyarene Derivatives
12 5 - Nitosalicylic acid
13 3 - Nitosalicylic acid
14 2- Nitro-3-hydroxybenzoic acid
15 2 - Nitro-5-hydroxybenzoic acid
16 3,4 - Dihydroxy-5-nitrobenzaldehyde
(Alkylamino)arene Derivatives
17 3 - (Dimethylamino) phenol
18 3 - (Diethylamino) phenol
19 3 - Amino phenol
20 4 - Diethylaminosalicyladehyde
21 4 - (Aminomethyl) aniline
22 N - benzyl-2-(2-methoxyphenoxy) ethylamine
23 Methyl-4-(butylamino) benzoate
24 2-(2-chlorophenyl) ethanamine
Anisole Derivatives
25 1-chloro-3-mrthoxy-2-methylbenzene
Group K Chiral Resolution Derivatives 10 No Changes

1 (R)-(+)-1 Phenylethylamine
2 (S)-(+)-1 Phenylethylamine
3 D - 2 - hydroxy-2-phenylacetic acid
4 L-(+)-Mendelic acid
5 (S)-(-)-Indoline-2-carboxylic acid
6 (S)-(-)-tetrahydro-2-furoic acid
Group L Ethylene Oxide an Isobutylene Intermediates 75 No Changes
Aryl Ethylene Oxide Derivatives

1 4 - (2 - methoxyethyl)phenol
2 4 - (2 - hydroxyethyl)phenol
3 2 - (4 - (tert - butyl)phenyl)ethanol
Aliphatic ethylene oxide derivatives
4 2 - (2 - chloroethoxy)ethanol
5 2 - (diisopropylamino)ethanol
6 2 - (tert - butylamino)ethanol
7 2 - (ethyl(phenyl)amino)ethanol
8 2- Chloro Ethanol
Butylates Aryl Derivatives
9 2,6 - di - tert-butyl-4-(2-hydroxyethyl)phenol
10 2,6 - di - tert-butyl phenol
11 1-(tert-butyl)-4-methylbenzene
12 1,3,5-tri-tert-butylbenzene
13 2-bromo-4-(tert-butyl)phenol
Butylated Alkyl Derivatives
14 1,1-dimethylethyl chloride
Group Organomettalic Chemistry Derivatives (Grignard, 20 No Changes

M Lithiation, Coupling) with production
Citalopram Series capacity.
4-(4-(dimethylamino)-1-(4-fluorophenyl)-1-
1 Product no. 13
is proposed to
Phosphine Derivatives
be replaced.
2 Triphenyl phosphine
Alkyl Benzene Derivatives
3 1-(tert-butoxy)-4-pentylbenzene
4 4-tert.butoxy alkyl benzene/4-Hydroxy alkyl benzene
Biaryl Derivatives
5 4'-methyl-2-cyanobiphenyl
6 4'-chloro-2-nitro-1,1'-biphenyl
Methyl 4-acetamino-3-chloro-5-(4-chloro-2-fluoro-3-
7
methoxyphenyl)picolinate
8 4-Cyanobiphenyl
9 4-(2-Pyridinyl)Benzaldehyde
10 2,4-Difluorobiphenyl
Dialkyl Derivatives
11 2,2-dimethyl pentane
12 7-Bromo-1-heptene
13 8-chloro-1-octene
Boronic Acid Derivatives
14 4-Chlorophenyl boronic acid
15 2-(1,3,2-dioxaborinan-2-yl)pyridine
2-(4-chloro-2-fluoro-3-methoxyphenyl)-1,3,2-
16
dioxaborinane
17 (4-chloro-2-fluoro-3-methoxyphenyl)boronic acid
18 3-Furanboronic acid
19 Dimethyl thiophen-2-ylboronate
20 Phenylboronic acid
Styrene Derivatives
21 1-propyl-4-vinylbenzene
22 4-vinylphenyl acetate
23 1-chloro-4-vinylbenzene
Aliphatic Hydroxy derivatives
24 oct-1-en-3-ol
25 4-methyl-3-decen-5-ol
26 3-methyl-1-phenylpentan-3-ol
2-methyl-1-phenylpropan-2-ol/dimethyl phenyl ethyl
27
carbinol
UPDATED PRODUCT LIST AFTER REMOVAL OF ABOVE HIGHLIGHTED PRODUCTS
AND ADDITION OF SOME NEW PRODUCTS:
PRODUCT NAME AND CAPACITY

Group Capacity as per
Product Name
No. CC&A
A Research & Development (R & D) Centre along with Pilot Plant and 10 MT/Month
Crams Products
Note:-
Chemistry Competencies (Group/Molecule)
 Hydrogenation/ asymmetric hydrogenation
 Chiral chemistry
 Organometallic chemistry (Grignard, organolithiation)
 Coupling reactions (Suzuki-Miyaura, Heck)
 Photochemistry
 Homogeneous catalysis
 Heterogeneous catalysis
 Exothermic chemistry (azide chemistry, ozonalysis) and
others
B Active Pharmaceuticals Intermediates 25
C Hydrogenation Derivatives 70
D Halogenation Derivatives 20
E Eatherification 75
F Specialty Chemicals (Electronic Chemicals, Fragrance & Flavors and 40
Specialty Monomers and Polymers)
G Heterocyclic Derivatives / Polycyclic Derivatives 40
H Oxidation Derivatives 40
I Carboxylic Acid Derivatives 30
J Basic Aromatic Intermediates 20
K Chiral Resolution Derivatives 10
L Ethylene Oxide an Isobutylene Intermediastes 75
M Organomettalic Chemistry Derivatives (Grignard, Lithiation, 20
Coupling)
Total 475
The detailed Product list for other groups are given below further to this table
Production Remarks
Group
Product Name (MT/Mont
No.
h)
Group B Active Pharmaceuticals Intermediates 25 No changes

MEP Derivatives
1 1-(4-(2-methoxyethyl)phenoxy)propan-2-ol
(RS)-1-(Isopropylamino)-3-[4-
2
(methoxyethyl)phenoxy]propan-2-ol
3
2-propanol succinate
4
2-propanol L-(+)-tartrate
(S)-1-(isopropylamino)-3-(4-(2-
5
methoxyethyl)phenoxy)propan-2-ol
Citalopram Series
S-(+)-4-(4-(dimethylamino)-1-(4-fluorophenyl)-1-
6
1-[3-Dimethylamino)propyl]-1-(4-flurophenyl)-1,3-
7
dihydro-5-isobenzofurancarbonitrile hydrobromide
S-(+)-1-[3-dimethylamino)propyl]-1-(4-fluorophenyl)-
8
1,3-dihydro-5-isobenzofurancarbonitrile oxalate
Metoprolol Derivatives
1-(4-((2-isopropoxyethoxy)methyl)phenoxy)-3-
9
(isopropylamino)propan-2-ol
Etodolac Derivatives
10 Etodolac
Atovaquone Derivatives
2-(4-(4-chlorophenyl)cyclohexyl)-3-hydroxynaphthalene-
11
1,4-dione
Mesalamine Derivatives
Group C Hydrogenation Derivatives 70 Product

Secondary amine Derivatives number 9 and
10 are newly
1 (2R, 3R, 4R, 5S)-6-(octylamino)hexane-1,2,3,4,5-pentaol
proposed.
(2R, 3R, 4R, 5S)-6-(Methylamino)hexane-1,2,3,4,5-
2
pentaol
(2R, 3R, 4R, 5S)-6-(ethylamino)hexane-1,2,3,4,5-
3
pentaol
Piperidine Derivatives
4 4-Piperidine Carboxylic Acid
5 4-Piperidine Carboxamide
6 2-aminomethylpiperidine
7 2-Piperidineethanol
Benzhydrol Derivatives
8 a,a-Diphenyl-4-piperidinemethanol
9 2-methyl-4-phenylbutan-2-ol
10 Coranol
Cyclohexyl Derivatives
11 1,3-Cyclohexanedione
12 Trans-4-Isopropylcyclohexanecarboxylic acid
13 Trans-4-Amino cyclohexanol
14 Ethyl 4-oxocyclohexanecarboxylate
Benzylamine Derivatives
15 3-Amino Benzylamine
16 2-Chloro Benzylamine
Chiral Amine Derivatives
(S)-2-chloro-N-(2-ethyl-6-methylphenyl)-N-(1-
17
methoxypropan-2-yl)acetamide
Benzenebutanoic acid, β-[[(1,1-
18 dimethylethoxy)Carbonyl]amino]-2,4,5-trifluro-,ethyl
ester,(βR)
19 (R)-1-(naphthalen-1-yl)ethanamine
Chiral Alcohol Derivatives
20 (R)-1-(3,5-bis(trifluoromethyl)phenyl)ethanol
21 3-(dimethylamino)-1-(thiophen-2-yl)propane-1-one
Benzyl Alcohol Derivatives
22 4-(2-amino-1hydroxyethyl)phenol
23 3-(hydroxymethyl)phenol
24 3-Phenoxy Benzyl Alcohol
Amine Arene Derivatives
25 2-Ethyl aniline
27 3-Aminosalicylic Acid
30 N-(4-Amino-2,5-dimethylphenyl)acetamide
31 N-(4-Amino-5-chloro-2-methylphenyl)acetamide
32 4'-chloro-[1,1'-biphenyl]-2-amine
33 3- Amino-4-toluic acid
34 2,5-Dimethyl-1,4-phenylenediamine
35 2-Chloro-5-methyl-1,4-phenylenediamine
36 3,3'-Diamino-4,4'-dihydroxydiphenyl sulfone
Alkyl Derivatives
37 N',N'-di-tert-butylethane-1,2-diamine
38 N',N'-dimethylethane-1,2-diamine
Group No Changes
Halogenation Derivatives 20
D
Benzylbromide Derivatives
1 1-(bromomethyl)-4-(trifluoromethoxy)benzene
2 4'-(bromomethyl)-[1,1'-biphenyl]-2-carbonitrile
(S)-2-Chloropropionic Acid / Esters Derivatives
3 2-Chloropropionic acid, ethyl ester
4 2-Chloropropionic acid, methyl ester
Halogenated Aryl Derivatives
5 3-(bromomethyl)pyridine
6 4-(chloromethyl)pyridine
7 4-Bromo-2,6-diisopropylaniline
8 2-bromophenol
9 3-chloro-2,6-diethylaniline
Naphthoquinone Derivatives
10 2-chloronaphthalene-1,4-dione
11 2,3-Dichloro-1,4-Naphthoquinone
Group No Changes
Eatherification 75
E with
(S)-2-Chloropropionic Acid / Esters Derivatives production
1 capacity.
(R)-2-(4-Hydroxyphenoxy) propionic acid
(R)-2-(Aryloxy)propionic Acid, Esters derivatives
2 (R)-2-(4-Hydroxyphenoxy)propionic acid, methyl ester Partial
3 (R)-2-(4-Hydroxyphenoxy)propionic acid, ethyl ester Effluent
4 Methyl-(R)-2-{4(2,4- generated
dichlorophenoxy)phenoxy}propaonate from this
group will be
5 Propynyl-(R)-2-[4-[(5-chloro-3-fluoro-2-pyridinyl)oxy]
now sent to
phenoxy] propanoate
common MEE
6 Butyl-(R)-2-(4-((5-(Trifluoromethyl)Pyridin-2- facility of
YL)Oxy)Phenoxy) Propanoate ‘GECL CETP ’
7 Methyl-(R)-2-{4-[3-chloro-5-(trifluoromethyl)-2- as new
pyridyloxy]propanoate facility
8 Ethyl (R)-2-[4-(6-chloroquinoxalin-2- Stored.
yloxy)phenoxy]propanoate
9 Ethyl-(R)-2-[4-{6-chloro-2-
benzoxazolyloxy}phenoxy]propanoate
10 Butyl-(R)-2-[4-(4-Cyano-2-Fluorophenoxy)
Phenoxy]Propanoate
Aryl ether Derivatives
11 2-(3-Phenoxyphenyl)propionic acid
12 2-(2-Methoxyphenoxy)ethylamine
13 4-Phenoxy-2, 6-diisopropyl aniline
14 4-Methoxy-3-[3-(4-morpholinyl)propoxy)benzonitrile
15 4-Fluoro-3-phenoxybenzaldehyde
16 2,6-Diisopropyl-4-phenoxyphenylthiourea
17 1-Tert-butyl-3-(2,6-Diisopropyl-4-henoxyphenyl)thiourea
18 2,6-Diisopropyl-4-phenoxy phenyl isothiocyanate
Specialty Chemicals (Electronic Chemicals, 40 Product no.

Group F Fragrance & Flavors and Specialty Monomers and 10 and 12 are
Polymers) newly
Cyclohexanone Derivatives proposed
1 4-Propyl Cyclohezanone products.
2 4-(4'-propylcyclohexyl)phenol
(Cyclohexyl)Phenyl Derivatives
3 Trans-(4'-propylcyclohexyl) cyclohexanone
4 4-(Trans-4-propylcyclohexyl) benzoic acid
5 (4-Trans-4-propylcyclohexyl) phenyl boronic acid
Cyclohexyl aryl Derivatives
6 4-(4-chlorophenyl) cyclohexanecarboxylic acid
OLED Derivatives
7 4 - Vinylphenylboronic Acid
8 B-[10-(2-naphthalenyl)-9-anthracenyl] boronic acid
9 4-(naphthalene-2-yl) boronic acid
Fragrance & Flavors
10 PPC Polyol
11 3-(4-Methoxyphenyl)-2-Metylpropanal
12 Trimethylolpropane trisorbate
Specialty Monomers and Polymers
13 Tetrahydro-2H-pyran-2-one
14 5-(1H-benzo[d]imidazol-2-yl)pentan-1-amine
15 2-methyl-1,2-oxaphospholan-5-one 2-oxide
16 Boron trichloride-N,N-dimethyloctylamine
Group 40 No changes
Heterocyclic Derivatives / Polycyclic Derivatives
G
Anthraquinone Derivatives
1 1,4-Dihydroxyanthraquinone
2 2,3-dihydro-9,10-dihydroxy-1,4-anthracenedione
Indole Derivatives
3 7-Ethyl Tryptophol
4 Methyl indol-6-carboxylate
5 Indoline
Phthalic acid Derivatives
6 5-nitro isophthalic acid
7 5 carboxyphthalide
Furan Derivatives
8 2,3-dihydro furan
9 2,5-Dihydrofuran
Imidazole Derivatives
10 1- methyl-1H-imidazole
11 2-Butyl-4-Chloro-5-Formylimidazole
Thiophene Derivatives
12 2-(thiophen-2-yl)ethanamine
13 2-(thiophen-2-yl)ethanol
Quinazoline Derivatives
14 4-(4-(tert-butyl)phenethoxy)quinazoline
Tetrahydrofuran Derivatives
15 1[(2S)-tetrahydro-2-furanyl]-ethanone
Pyridine Derivatives
16 4-pyridinecarboxylic acid
17 4-pyridinecarboxamide
18 4-pyridinemethylamine
19 2-(Pyridin-2-yl)ethanol
Pyran Derivatives
20 3,4-Dihydro-2H-pyran
Carbonate Derivatives
Bis (2,5-dioxopyrrolidin-1-yl)carbonate,[N,N-
21
discuccinimidyl carbonate]
Piperazine Derivatives
22 1-(2,3-dichlorophenyl)piperazine hydrochloride
Thiazole Derivatives
23 Thiazol-5-ylmethanol
Diphenyl Methane Derivatives
1,1'-(methylenebis(4,1-phenylene))bis(1H-pyrrole-2,5-
24
dione)
Pyrimidine Derivatives
2-(2,2-Difluoroethoxy)-N-(5,8-
25 dimethoxy[1,2,4]triazol[1,5,7] pyrimidine-2-yl)-6-
(trifluoromethyl)benzenesulfonamide
Sulfamide Derivatives
26 Sulfamide
Group 40 Product no. 6

Oxidation Derivatives
H and 9 are newly
Aryl Aldehyde Derivatives proposed
products.
1 4-hydroxy benzaldehyde (PHB)
2 4-methoxy benzaldehyde / p-anesaldehyde (PAA)
4 2,6-dichlorobenzaldehyde
6 2-Thiophenecarboxylic acid
7 2-amino-3,5-dibromobenzaldehyde
Aryl Carboxylic Acid Derivatives
8 4-(tert-butyl)benzoic acid
9 2-Thiophenecarbonyl chloride
10 2,4-Dichlorobenzoic acid
11 3,5-di-t-butyl-4-hydroxy benzoic acid
12 3-methoxy-2-methylbenzoic acid
13 2-ethoxy benzoic acid
14 3-amino-4-methylbenzoic acid
15 Mafenamic acid
16 4-aminobenzoic acid
Keto Aryl Derivatives
17 Naphthalene-1,4-dione
Pyromelllitic Anhydride (benzo(1,2-c;4,5-c')difuran-
18
1,3,5,7-tetraone
Group I Carboxylic Acid Derivatives 30 Product no. 1

Benzonitrile Derivatives and 3 are newly
proposed
1 2-chlorobenzonitrile
product.
2 4-Hydroxy benzonitrile
3 5-Cyano-3H-isobenzofuranone
4 4-chlorobenzonitrile
5 2-amino-4-chloro benzonitrile
6 2,6-dichlorobenzonitrile
7 4 - chlorophenyl benzene butane nitrile
Aryl Carboxylic Acid Ester Derivatives
10 Methyl 4-amino Benzoate
11 tert-Butyl 4-(chloromethyl)benzoate
12 Dimethyl-5-aminoisophthalate
13 Methyl-3-amino-4-toluate
14 Ethyl paraben
15 Propyl paraben
16 Ethyl-4 amino benzoate
17 4'-methyl-2-biphenyl carboxylic acid methyl ester
18 Hexyl-3,5-di-tert-butyl-4-hydroxybenzoate
Aryl Acetyl Derivatives
19 N-(2,5-Dimethylphenyl)acetamide
20 N-(5-Chloro-2-methylphenyl)acetamide
21 3-Nitrophenyl acetate
22 2-Acetylthiophene
Aryl Acid chloride Derivatives
23 3-methoxy-2methyl benzoyl chloride
Benzamide Derivatives
24 2-Chloro-n-(4'-chloro-[1,1'-biphenyl]-2-yl)nicotinamide
25 4-chloro-2nitro benzamide
Group J Basic Aromatic Intermediates 20 Product no. 12

Aryl Hydrazine Derivatives and 13 are
newly proposed
1 2 - Ethyl Phenyl Hydrazine Hydrochloride
products.
2 p-Sulphonamide phenyl hydrazine hydrochloride
Nitroarene Derivatives
3 2-Cholro - 5-nitro benzoic acid
4 3-Nitro 2-Cholro benzoic acid
5 N - (2,5- Dimethyl-4-nitophenyl) acetamide
6 N - (5-Chloro-4-nitro-2-methylphenyl) acetamide
7 3-Nitro -4-toluic acid
10 5 - Nitovanillin
11 3,3'-Diamino-4, 4' - dihydroxydiphenylsulfone
Hydroxyarene Derivatives
12 Bifenthrin alcohol
13 1-[2-(2-Hydroxyethoxy)ethyl]piperazine
14 2- Nitro-3-hydroxybenzoic acid
15 2 - Nitro-5-hydroxybenzoic acid
16 3,4 - Dihydroxy-5-nitrobenzaldehyde
(Alkylamino)arene Derivatives
17 3 - (Dimethylamino) phenol
18 3 - (Diethylamino) phenol
19 3 - Amino phenol
20 4 - Diethylaminosalicyladehyde
21 4 - (Aminomethyl) aniline
22 N - benzyl-2-(2-methoxyphenoxy) ethylamine
23 Methyl-4-(butylamino) benzoate
24 2-(2-chlorophenyl) ethanamine
Anisole Derivatives
25 1-chloro-3-mrthoxy-2-methylbenzene
Group K Chiral Resolution Derivatives 10 No Changes

1 (R)-(+)-1 Phenylethylamine
2 (S)-(+)-1 Phenylethylamine
3 D - 2 - hydroxy-2-phenylacetic acid
4 L-(+)-Mendelic acid
5 (S)-(-)-Indoline-2-carboxylic acid
6 (S)-(-)-tetrahydro-2-furoic acid
Group L Ethylene Oxide an Isobutylene Intermediates 75 No Changes
Aryl Ethylene Oxide Derivatives

1 4 - (2 - methoxyethyl)phenol
2 4 - (2 - hydroxyethyl)phenol
3 2 - (4 - (tert - butyl)phenyl)ethanol
Aliphatic ethylene oxide derivatives
4 2 - (2 - chloroethoxy)ethanol
5 2 - (diisopropylamino)ethanol
6 2 - (tert - butylamino)ethanol
7 2 - (ethyl(phenyl)amino)ethanol
8 2- Chloro Ethanol
Butylates Aryl Derivatives
9 2,6 - di - tert-butyl-4-(2-hydroxyethyl)phenol
10 2,6 - di - tert-butyl phenol
11 1-(tert-butyl)-4-methylbenzene
12 1,3,5-tri-tert-butylbenzene
13 2-bromo-4-(tert-butyl)phenol
Butylated Alkyl Derivatives
14 1,1-dimethylethyl chloride
15 O-tolyl benzonitrile
Group Organomettalic Chemistry Derivatives (Grignard, 20 13 is newly

M Lithiation, Coupling) proposed
Citalopram Series product.
4-(4-(dimethylamino)-1-(4-fluorophenyl)-1-
1
Phosphine Derivatives
2 Triphenyl phosphine
Alkyl Benzene Derivatives
3 1-(tert-butoxy)-4-pentylbenzene
4 4-tert.butoxy alkyl benzene/4-Hydroxy alkyl benzene
Biaryl Derivatives
5 4'-methyl-2-cyanobiphenyl
6 4'-chloro-2-nitro-1,1'-biphenyl
Methyl 4-acetamino-3-chloro-5-(4-chloro-2-fluoro-3-
7
methoxyphenyl)picolinate
8 4-Cyanobiphenyl
9 4-(2-Pyridinyl)Benzaldehyde
10 2,4-Difluorobiphenyl
Dialkyl Derivatives
11 2,2-dimethyl pentane
12 7-Bromo-1-heptene
13 tert-Butyl chloroacetate
Boronic Acid Derivatives
14 4-Chlorophenyl boronic acid
15 2-(1,3,2-dioxaborinan-2-yl)pyridine
2-(4-chloro-2-fluoro-3-methoxyphenyl)-1,3,2-
16
dioxaborinane
17 (4-chloro-2-fluoro-3-methoxyphenyl)boronic acid
18 3-Furanboronic acid
19 Dimethyl thiophen-2-ylboronate
20 Phenylboronic acid
Styrene Derivatives
21 1-propyl-4-vinylbenzene
22 4-vinylphenyl acetate
23 1-chloro-4-vinylbenzene
Aliphatic Hydroxy derivatives
24 oct-1-en-3-ol
25 4-methyl-3-decen-5-ol
26 3-methyl-1-phenylpentan-3-ol
2-methyl-1-phenylpropan-2-ol/dimethyl phenyl ethyl
27
carbinol
ANNEXURE – III
MANUFACTURING PROCESSES OF PROPOSED NEW PRODUCTS ALONG WITH MASS BALANCE AND POLLUTION
LOAD COMPARISON WITH REPLACED PRODUCTS
Spent
Quantity of Quantity of Quantity of
catalyst/spent
water WW Hazardous Air pollutant
Particular Group Name of product acid/spent
consumption generation waste
solvent
(L/Day) (L/Day) (Kg/Batch) (Kg/Batch) (Kg/Batch)
Distillation
Existing Diphenylmethanol 11424 4466 Residue Nil
10
Distillation
Proposed 2-methyl-4-phenylbutan-2-ol 392 495.6 Residue Nil
74
C
Distillation
Existing 4-Chlorobenzhydrol 11648 4676 Residue Nil
10
Distillation Spent Catalyst
Proposed Coranol 0 0 Residue (Rany Nikal)
109 3.75
NaCl
771
Distillation
1-methoxy-4-(prop-1-en-1-yl)
Existing 4000 3563.2 Residue --
benzene
75
Raney Nickel
F 71.73
NaCl
50
Proposed PPC Polyol 0 0 Distillation --
Residue
80
Distillation
H3PO4
Residue
293.3 2633
3-(4-(Tert-butyl)phenyl)-2- catalyst
Existing 10384.8 4818.72
methylpropanal
111
Raney Nickel
74.13
NaCl
50
Proposed Trimethylolpropane trisorbate 6000 3830.4 Distillation Nil
Residue
80
Distillation
Residue
4-(diethylamino)-2-hydroxy 286
Existing 6032 5763.2 Nil
benzaldehyde
Catalyst
86
Distillation
Proposed H 2-Thiophenecarboxylic acid 0 4000 Residue Nil
153.5
Existing 2-Nitro Benzoic acid 3228.8 3475.2 -- Nil

Distillation
SO2
Proposed 2-Thiophenecarbonyl chloride 0 328 Residue Nil
75 575
Distillation
25% HCl
Residue
Existing 2-Hydroxy benzonitrile 2484 0 296 2760
Sodium Sulphite
I
2300
Distillation
Proposed 2-chlorobenzonitrile 0 150 Residue Nil
75
Solid Waste
Existing J 5 - Nitosalicylic acid 4992 5696 --
25
Distillation
Proposed Bifenthrin alcohol 0 4032 Residue --
358
Solid Waste
Existing 3 - Nitosalicylic acid 4992 5696 --
25
NaCl Toluene
50 480
1-[2-(2-
Proposed 2000 5000 Distillation
Hydroxyethoxy)ethyl]piperazine
Residue
80
Distillation
Group L THF
--- 10500 15303 Residue
(max.)
350 8270
L
Distillation
THF
Proposed O-tolyl benzonitrile (OTBN) 0 8706 Residue
330 8148
Solid waste THF

25 1910
Existing 8-chloro-1-octene 3056 1508
Residue Ethyle Acetate
M 162 3920
Distillation
Toluene
Proposed tert-Butyl chloroacetate 558.4 408.8 Residue
75 1985
Summary:
Remarks
There will be no increase in water consumption and wastewater generation quantity. Also quality of effluent generated due to replacement of
existing products will be less pollutant than existing effluent quality.
The overall quantity of distillation residue will not increase due to proposed replacements of the products.
SO2 gas generated from replaced product will be treated through existing alkali scrubber only.
ANNEXURE – IV
Details on Water Consumption and Wastewater Generation
Details of Water Consumption
Sr. No. Description KL / Day
Pilot Plant 10
1. Process R&D 5
Process 111
2. Boiler 80
3. Cooling 100
4. Washing 10
5. Scrubber 20
Total Industrial 336
6. Domestic 20
7. Gardening 8
Grand Total 364
Note:
There is no change in proposed water consumption.
Details of Waste Water Generation
Description KL / Day
Pilot Plant 10
1. Process R&D 4
Process 106
2. Boiler 10
3. Cooling 6
4. Washing 10
5. Scrubber 15
Total Industrial 161 *
6. Domestic 20
7. Gardening 0
Grand Total 181
Note: * Out of 161 KL/Day of effluent, about 16 KL/Day of waste water generated from Boiler
blow down and cooling tower blow down shall be used in to Scrubber as a absorbing media.
Hence only 145 KL/Day is treated in to the ETP as under:

Stream-1 – 15 KLD dilute stream is sent to CETP of M/s. GECL
Stream-2 – 90 KLD Low TDS & low COD stream is given primary and SBT treatment followed by
RO plant.
Stream-3 – 40 KLD High TDS & high COD stream is treated into inhouse MEE followed by RO
plant
Due to proposed amendment, overall quantity of waste water generation will remain same as
per existing CCA conditions.
However, stream B (Low COD and Low TDS) will be segregated into 2 streams.
1. 75 KLD effluent will be treated as per existing treatment scheme.

2. 15 KLD effluent generated from manufacturing of Group ‘E’ products will
be now sent to common MEE facility of ‘GECL CETP ’ as new facility Stored.
Treatment scheme for stream 1 and stream 3 will remain same as per existing operating
condition
EXISTING WATER BALANCE DIAGRAM
Water Consumption – 364

KLD
Washing Scrubber Boiler Cooling Pilot Plant Process R&D Gardening Domestic
10 KLD 20 KLD 80 KLD 100 KLD 10 KLD 111 KLD 5 KLD 8 KLD
20 KLD
10 KLD 15 KLD 10 KLD 6 KLD 10 KLD 106 KLD 4 KLD
20 KLD
40 KLD :- 11 KLD
55 KLD
16 KLD COD >20,000 mg/lit
Recycle in to Scrubber
15 KLD :-
TDS > 15,000 mg/lit
pH Correction & Solvent COD : 4,000 mg/lit
90 KLD
Stepper Column to 6000 mg/lit
:-COD : 15,000 to 20,000 mg/lit
TDS < 15,000 mg/lit

Multi Effect Evaporator / ATFD
Primary Treatment Phanton
MEPPL
Treatment
Condensate Water
SBT Send to CETP of
M/s. GECL, Sachin
Common RO Plant
Common RO Plant
RO Reject Water RO Permeate Water

RO Permeate Water RO Reject Water
35 KLD
70 KLD 5 KLD
20 KLD
Subjected to MEE / Recycle in to Utilities

Recycle in to Utilities Subjected to MEE /
MEPPL
MEPPL
PROPOSED WATER BALANCE DIAGRAM
Water Consumption – 364 KLD
Washing Scrubber Boiler Cooling Pilot Plant Process R&D Gardening Domestic
10 KLD
1. 20 KLD 80 KLD 100 10 KLD 111 KLD 5 KLD 8 KLD 20 KLD
KLD
10 15 10 6 KLD 10 106 4 KLD
20
KLD KLD KLD KLD KLD
40 KLD
55 11
16 KLD KLD :- Septic Tank / Soak
Recycle in to KLD
KLD Pit System
Scrubber 15
pH Correction & Solvent KLD :-
75 15 Stepper Column
KLD
:-
Multi Effect Evaporator / ATFD Phanton
Primary Treatment Common MEE
MEPPL Treatment
facility of
GECL
Condensate Water
SBT
Send to CETP of
M/s. GECL, Sachin
Common RO Plant
Common RO Plant
RO Reject Water RO Permeate Water

RO Permeate Water RO Reject Water
27 KLD
KLD 5 KLD
20 KLD
Subjected to MEE / Recycle into Utilities

Recycle in to Utilities Subjected to MEE /
MEPPL
MEPPL
2. EFFLUENT TREATMENT DISPOSAL DETAILS
Sr. Brief details of Remarks

Stream Quantity
No. Disposal
A Stream 1 15 KL/Day Shall be sent to CETP of

M/s. GECL
Dilute Stream :
(COD – 4,000 to
6000 mg/lit)
No Changes
Shall be generated from the manufacturing of Group D, G, I & K
and R & D process, shall be given Phanton treatment and then
sent to CETP of M/s. GECL for further treatment and final
disposal.
B Stream 2 75 KL/Day Shall be given Primary Quantity is reduced

Low TDS (< 15,000 and SBT treatment and from 90 KLD to 75
KLD due to
mg/lit) & low COD feed in to R. O. Plant
changes in
(15,000 to 20,000 products as given
mg/lit) in group E.
Shall be generated from the manufacturing of Group C, F & J,

Rest 15 KLD
from pilot plan, washing and scrubber shall be given Primary effluent
and SBT Treatment and passed though Common R O Plant. generated from
group ‘E’ will be
From R. O. Plant ….
sent to common
RO Permeate Water shall be recycle in to utilities. And RO MEE facility of
Reject Water shall be subjected to Common MEE / MEPPL. ‘GECL’
C Stream 3 40 KL/Day Shall be subjected to No Changes

Concentrated Multi Effect Evaporator /
Stream – High TDS shall be sent to MEPPL
(> 15,000 mg/lit) &
High COD (> 20,000
mg/lit)
Shall be generated from the manufacturing of B, H, L & M shall
be subjected to Multi Effect Evaporator after passed through pH
Correction &Solvent Stepper Column. The condensate water
shall be passed though Common R O Plant. From R. O. Plant ….
RO Permeate Water shall be recycle in to utilities. And RO

Reject Water shall be subjected to Common MEE / MEPPL.
D Stream 4 15 KL/Day Shall be sent to Proposed change

Concentrated common MEE
stream with high facility of GECL
TDS after neutralization
ANNEXURE – V
SOLID / HAZARDOUS WASTE MANAGEMENT SYSTEM
Waste
Cat. Solid / Hazardous
Source of Waste generation Disposal
No. Waste
Quantity
34.3 ETP Sludge From ETP 250 MT / Year Collection / Storage / Transportation /
sent to TSDF Site
5.1 Used Oil From plant & 100 Liters/Month Collection / Storage / Transportation /
machineries (i.e. 0.085 sent to registered recycler / reuse as a
MT/Month) lubricant
33.3 Discarded containers / From material 150 Nos./Month Collection / Storage / Transportation /
bags / liners / Barrel0s packaging (i.e. 1.2 MT/Month) Supplier / sent to registered recycler
*600 Nos/month
(i.e. 4.8 MT/Month)
26.1 Process Sludge From Process 176 MT / Month Sent to TSDF site for suitable treatment &
final disposal
--- MEE Salt ** From Evaporator 50 MT / Month Collection / Storage / Transportation /

sent to TSDF Site
* Quantity of drums are proposed to be increased from 150 Nos/Month to 600 Nos./Month.
* * In case of Industry will operate own MEE for the treatment of concentrate effluent .
Source of Waste Proposed Total Disposal
No. Waste
28.2
Collection / Storage / Transportation /
25.6 MT/Month
Spent Catalyst# From Process Reused in to Process / send to
regeneration unit / sent to TSDF Site
19 MT / Month
Carbon Waste From Process Collection / Storage / Transportation /
manufacturing of Reused in to Process / send to
Group C, J regeneration unit / sent to TSDF Site
3 MT / Month
Raney Nickel From Process Collection / Storage / Transportation /
manufacturing of Reused in to Process / send to
Group F regeneration unit / sent to TSDF Site
Spent Solvent From Process As under ….

20.2 Collection / Recycle back in to the
Process / Storage / Transportation / to
TSDF site for suitable treatment
Spent Solvent From manufacturing of 160 MT / Month
Collection / Recycle back in to the
(Toluene) all group
Process for the manufacturing of all
group/ Storage / Transportation / send
to Authorized Recycler
# shows the additional quantity of spent catalyst which is generated from production of new product 2-MPB in group ‘C’
Cat. Solid / Hazardous Disposal
Source of Waste Proposed Total
No. Waste
Spent Solvent From manufacturing of 23.57 MT / Month

(Acetone) Group No. B, C, F, H, I,
Process for the manufacturing of
K
Group No. B, C, F, H, I, K / Storage
/ Transportation / send to
Authorized Recycler.
(Methanol) Group No. B, C, D, E,
Process for the manufacturing of
F, G, H, I, J, K
Group No. B, C, D, E, F, G, H, I, J,
K/ Storage / Transportation / send
to Authorized Recycler.
(IPA) Group No. B, C, G, K,
Process for the manufacturing
M
Group No. B, C, G, K, M / Storage /
Transportation / send to
Authorized Recycler
(MIBK) Group No. B
Process for the manufacturing
Group No. B/ Storage /
Transportation / send to
Authorized Recycler
No. Waste

Collection / Recycle back in to the Process
(BCP) Group No. B
for the manufacturing Group No. B /
Storage / Transportation / send to
Authorized Recycler
(THF) Group No. B, C, F, G, H,
for the manufacturing Group No. B, C, F, G,
I, J, L, M
H, I, J, L, M / Storage / Transportation /
send to Authorized Recycler
(Acetonitrile) Group No. B, G, I, M
for the manufacturing Group No. B, G, I, M
/ Storage / Transportation / send to
Authorized Recycler
(MDC) Group No. B, C, D, E, F,
for the manufacturing Group No. B, C, D, E,
G, I, J, K, M
F, G, I, J, K, M / Storage / Transportation /
send to Authorized Recycler
No. Waste

Collection / Recycle back in to the Process for
(2-IPE) Group No. B
the manufacturing Group No. B, / Storage /
Transportation / send to Authorized Recycler
(Ethanol) Group No. C, F, I, K
the manufacturing Group No. C, F, I, K /
Authorized Recycler
(Ethyl Acetate) Group No. C, D, E, F, G,
the manufacturing Group No. C, D, E, F, G, H,
H, I, J
I, J / Storage / Transportation / send to
Authorized Recycler
(Pyrolidine) Group No. C
the manufacturing Group No. C / Storage /
Transportation / send to Authorized Recycler
No. Waste

(Di Chloro Methane) Group No. C, E, G
for the manufacturing Group No. C, E, G, /
Authorized Recycler
(Oxo Carboxylic Acid) Group No. C
for the manufacturing Group No. C / Storage
/ Transportation / send to Authorized
Recycler
(EDC) Group No. C, D, E, F, G,
for the manufacturing Group No. C, D, E, F,
H, I, J
G, H, I, J/ Storage / Transportation / send
to Authorized Recycler
(Propanol) Group No. I
for the manufacturing Group No. I/ Storage
Recycler
No. Waste

(Methyl Cellosolve) Group No. C, J
for the manufacturing Group No. C, J/
Authorized Recycler
(Acetic Acid) Group No. C, E, F, H, I
for the manufacturing Group No. C, E, F, H,
I/ Storage / Transportation / send to
Authorized Recycler
(TMFB) Group No. D
for the manufacturing Group No. D /
Authorized Recycler
(Xylene) Group No. D, G, I
for the manufacturing Group No. D, G, I/
Authorized Recycler
No. Waste

Spent Solvent From manufacturing of
8.1 MT / Month for the manufacturing Group No. E, /
(Hydroquinone) Group No. E Storage / Transportation / send to
Authorized Recycler

16.5 MT / Month for the manufacturing Group No. E, /
(MEG) Group No. E Storage / Transportation / send to
Authorized Recycler

66 MT / Month for the manufacturing Group No. E, F/
(Phenol) Group No. E, F Storage / Transportation / send to
Authorized Recycler

16.6 MT / Month for the manufacturing Group No. E, H/
(DMF) Group No. E, H Storage / Transportation / send to
Authorized Recycler
No. Waste

(Di Ethyl Ether) Group No. F, M
for the manufacturing Group No. F, M /
Authorized Recycler
(Ether) Group No. F
for the manufacturing Group No. F /
Authorized Recycler
(n-hexane) Group No.F, G, L, M
for the manufacturing Group No. F, G, L, M /
Authorized Recycler
(Cyclo Hexane) Group No. F, J, L
for the manufacturing Group No. F, J, L /
Authorized Recycler
No. Waste

(ETOAc) Group No. F
for the manufacturing Group No. F /
Authorized Recycler
(2 – Ethyl Amine) Group No. G
for the manufacturing Group No. G /
Authorized Recycler
(Ethyl Glycol) Group No. G
Authorized Recycler
(terepthalic acid) Group No. G
Authorized Recycler
No. Waste
Spent Solvent From manufacturing of 0.12 MT / Month Collection / Recycle back in to the Process for
(2-butane 1, 4 - Diol) Group No. G the manufacturing Group No. G / Storage /
Transportation / send to Authorized
Recycler
(tert-Butanol) Group No.G, I the manufacturing Group No. G, I / Storage
Recycler
Spent Solvent From manufacturing of 14 MT / Month Collection / Recycle back in to the Process for
(tetra hydro furfuryl Group No. G the manufacturing Group No. G / Storage /
alcohol) Transportation / send to Authorized
Recycler
(trichloroacetaldehyde) Group No. G the manufacturing Group No. G / Storage /
Recycler
Cat.
Solid / Hazardous Waste Source of Waste Proposed Total Disposal
No.

(Sulfuryl dichloride) Group No.G
Authorized Recycler
(2-(2- Group No. G
chlorophenyl)acetonotrile) Storage / Transportation / send to
Authorized Recycler
(2,6-dichloro toluene) Group No. H, I
for the manufacturing Group No. H, I /
Authorized Recycler
(2,6-dichloro benzoyl Group No. H
for the manufacturing Group No. H /
chloride) Storage / Transportation / send to
Authorized Recycler
No. Waste
(Diethyl amine) Group No. H, J the manufacturing Group No. H, J / Storage
Recycler
(2, 4 DHB) Group No. H the manufacturing Group No. H/ Storage /
Recycler
(Organic layer DTBP) Group No. H the manufacturing Group No. H/ Storage /
Recycler
(2,3-dimethylaniline) Group No. H the manufacturing Group No. H/ Storage /
Recycler

No. Waste
(Dimethyl Sulohoxide) Group No. J the manufacturing Group No. J/ Storage /
Recycler
(Chloro Benzene) Group No.I, J the manufacturing Group No. I, J/ Storage /
Recycler
(Resorcinol) Group No. J the manufacturing Group No. J/ Storage /
Recycler
(Dichloro benzene) Group No. J the manufacturing Group No. J/ Storage /
Recycler
No. Waste
(Di methyl amine) Group No. J the manufacturing Group No. J/ Storage /
Recycler
(Amine) Group No. J the manufacturing Group No. J/ Storage /
Recycler
(1-(2-chloroethoxy)-2- Group No. J the manufacturing Group No. J/ Storage /
methoxy benzene) Transportation / send to Authorized
Recycler
(2-(2-chlorophenyl) Group No.J the manufacturing Group No. J/ Storage /
acetonitrite) Transportation / send to Authorized Recycler
No. Waste
Spent Solvent From manufacturing of 1.8 MT / Month Collection / Recycle back in to the Process
(1,3-dichlor-2-methyl Group No. J for the manufacturing Group No. J/ Storage
benzene) / Transportation / send to Authorized
Recycler
(Isobutylene) Group No. L, M for the manufacturing Group No. L, M /
Authorized Recycler
(MCB) Group No. I, L for the manufacturing Group No. I, L /
Authorized Recycler
(PCB) Group No. L for the manufacturing Group No. L/ Storage
Recycler
No. Waste
Spent Solvent From manufacturing of 6 MT / Month Collection / Recycle back in to the Process
(4-chlorobenzoic acid) Group No. I for the manufacturing Group No. I /
Authorized Recycler
(4-chloro-2- Group No. I for the manufacturing Group No. I /
nitrobenzonitrile) Storage / Transportation / send to
Authorized Recycler
(4-hydroxybenzoic Group No. I for the manufacturing Group No. I /
acid) Storage / Transportation / send to
Authorized Recycler
(Triethyl amine) Group No. I for the manufacturing Group No. I /
Authorized Recycler
No. Waste

Spent Solvent
From manufacturing of for the manufacturing Group No. I /
(4-chloro-2-nitro 3.5 MT / Month
Group No. I Storage / Transportation / send to
benzoic acid)
Authorized Recycler
Spent Solvent From manufacturing of for the manufacturing Group No. I /
7.2 MT / Month
(SOCl2) Group No. I Storage / Transportation / send to
Authorized Recycler
Spent Solvent From manufacturing of for the manufacturing Group No. M /
7.15 MT / Month
(Dimethoxy ethane) Group No. M Storage / Transportation / send to
Authorized Recycler
Spent Solvent
From manufacturing of for the manufacturing Group No. M /
(1, 4 - dichloro 6 MT / Month
Group No. M Storage / Transportation / send to
benzene)
Authorized Recycler
No. Waste
(NMP) Group No. I for the manufacturing Group No. I /
Authorized Recycler
(1,2,4,5- Group No. H for the manufacturing Group No. H /
tetramethylbenzene) Storage / Transportation / send to
Authorized Recycler
Spent Solvent From manufacturing of Collection / Recycle back in to the Process
(Petroleum Ether) Group No. M for the manufacturing Group No. M/ Storage
3.1 MT / Month
Recycler
Spent Solvent From manufacturing of Collection / Recycle back in to the Process
(1-chloro-3-fluoro-2- Group No. M for the manufacturing Group No. M/
1 MT / Month
methoxybenzene) Storage / Transportation / send to
Authorized Recycler
No. Waste
(tert-butyl methyl Group No. M the manufacturing Group No. M / Storage /
ether) Transportation / send to Authorized Recycler
20.3 Distillation Residue From Process 157 MT / Month Collection / Storage / Transportation /
Redistilled / Sent to TSDF site for
incineration / sell to cement industries for co
processing
D2 KCl Solution From manufacturing of 255 MT / Month Collection / Storage / Transportation / sold
Group B as a by product
KCl Salt From manufacturing of 74 MT / Month Collection / Storage / Transportation / sold
Group E as a by product
D2 Pottasium Chloride From manufacturing of 4 MT/Month Collection / Storage / Transportation / sold
Group H as a by product
NaCl From manufacturing of 27 MT/Month Collection / Storage / Transportation / sold
Group C as a by product / send to TSDF site
No. Waste
D2 NaCl Salt From manufacturing of 31 MT/Month Collection / Storage / Transportation / sold

Group F as a by product / send to TSDF site
Spent HCl From manufacturing of 70 MT / Month Collection / Storage / reuse in to process /
Group D, G, J Sold as a By Product
Sodium Sulphite From manufacturing of 191 MT / Month Collection / Storage / Transportation / sold
Group D, E, I, J as a by product
30 % Sodium Bromide From manufacturing of 114 MT / Month Collection / Storage / Transportation / sold
Group D as a by product
KBr Solution From manufacturing of 100 MT / Month Collection / Storage / Transportation / sold
C1 Liq. NH3 Sol. From manufacturing of 27 MT / Month Collection / Storage / Transportation / sold
Alum From manufacturing of 95 MT/Month Collection / Storage / Transportation / sold

Group G, J as a by product
Sodium Acetate From manufacturing of 17 MT/Month Collection / Storage / Transportation / sold

Group G as a by product
No. Waste
C1 Ammonium Sulphate From manufacturing of 80 MT / Month Collection / Storage / Transportation / sold

Group I, J as a by product
2-Chloroethoxy ethanol From manufacturing of 3.5 MT / Month Collection / Storage / Transportation / Reuse
Group L / Sold as a by product
Na2SO4 From manufacturing of 44.5 MT / Month Collection / Storage / Transportation / send

Group I, J, K to TSDF site
4, 4 - Dimethyl From manufacturing of 10 MT/Month Collection / Storage / Transportation / sold

Biphenyl Group M as a by product / Reuse
D3 Magnesium Sulphate From manufacturing of 3.8 MT/Month Collection / Storage / Transportation / sold
Group M as a by product / send to TSDF Site
D3 Magnesium Sulphate From Manufacturing of 4 MT/Month Collection / Storage / Transportation / sold

Group M as a by product / send to TSDF Site
D3 Sodium Methyl From manufacturing of 90 MT/Month Collection / Storage / Transportation / sold

sulphate Group L as a by product / Reuse
DETAILS ON AIR POLLUTION
Stack Stack Attached Stack Height & Fuel

APCM
No. to Diameter Consumption
1. Steam Boiler Height - 30 Meters Natural Gas – As Natural Gas shall

Capacity : 4 Diameter - 1.0 3180 SM3/Day be use as fuel,
MT/Hr Meter adequate Stack
Height shall be
provided.
2. Thermopack Height – 15 Meters Natural Gas – 24 As Natural Gas / LDO

Capacity : 400 U Diameter – 0.3 SM3/Hr shall be use as fuel,
Meter OR adequate Stack
LDO – 40 Liters/Hr Height shall be
provided.
3. Thermopack Height – 15 Meters Natural Gas – 24 As Natural Gas / LDO

Capacity : 400 U Diameter – 0.3 SM3/Hr shall be use as fuel,
Meter OR adequate Stack
LDO – 40 Liters/Hr Height shall be
provided.
4. D. G. Set (Stand Height – 10 Meters Diesel As Diesel shall be use
by) – Cap: 750 Diameter – 0.03 100 Liters/Hr as fuel, adequate
KVA × 2 Meter Stack Height shall be
(Each) provided.
PROCESS GAS EMISSION
Stack Vent Height &

Vent Attached to Pollutants APCM
No. Diameter
1. Reactors Height – 15 Meters HCl, SO2, HBr Water Scrubber

followed by Alkali
Diameter – 0.3 Scrubber
Meter

followed by Alkali
Meter

followed by Alkali
Meter
There will be no change in process gas emission due to proposed amendment.

Basic Information, Form No. 1

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Basic Information, Form No.

Amendment in existing Environmental

M/s. Aether Industries Ltd.

(I) Basic Information

M/s. Aether Industries Limited

The proposed Amendment is for change

Stream ‘B’ – 90 KLD effluent; treated in

There will be replacement of some

Total area of the plot is 10500 sq.m.

1. Construction, operation or decommissioning of the Project involving actions,

Details thereof (with approximate

Permanent or temporary change

Clearance of existing land,

1.3 Creation of new land uses? NO Not applicable

1.5 Construction works? NO Not applicable

1.6 Demolition works? NO Not applicable

Temporary sites used for

Above ground buildings,

Underground works including

1.10 Reclamation works? NO Not applicable

1.12 Offshore structures? NO Not applicable

Production capacity will remain same.

For details of solid / hazardous waste

Facilities for treatment or There are no changes in quantity of

Facilities for long term housing

The existing infrastructure and transportation

New road, rail, air, waterborne

Closure or diversion of existing

1.20 New or diverted transmission NO Not applicable

1.22 Stream crossings? NO Not applicable

No ground water is being utilize for any of the

Changes in water bodies or the Proper storm water discharge is installed.

Ongoing activity during

Influx of people to an area in

1.29 Introduction of alien species? NO Not applicable

Loss of native species or genetic

1.31 Any other actions? NO Not applicable

Sr. Information / Checklist Yes/ Details thereof (with approximate

S. No. Information / Checklist Yes Details thereof (with approximate

3.2 Changes in occurrence of NO None

3.4 Vulnerable groups of people NO Not applicable

3.5 Any other causes NO NIL

Sr. Information / Checklist Yes Details thereof (with approximate

4.1 Spoil, overburden or mine NO NIL

For detail please refer Annexure V

4.5 Surplus product NO Not applicable.

4.7 Construction or demolition NO Not applicable. No additional construction will be

4.8 Redundant machinery or NO Not applicable

4.9 Contaminated soils or other NO Not applicable

4.10 Agricultural wastes NO NIL

4.11 Other solid wastes NO NIL

Sr.No. Information Details thereof (with approximate

Emissions from combustion of fossil

For detail please refer in Annexure VI

There shall be fugitive emissions during

Dust or odors from handling of

5.6 Emissions from incineration of waste NO No such activity is proposed

Emissions from burning of waste in

5.8 Emissions from any other sources NO NIL

Sr. Details thereof (with approximate

The noise levels near the sources such as D.

From industrial or similar All machinery / equipment is having barriers /