Professional Documents
Culture Documents
of
Proposed Manufacturing Unit of Pharmaceuticals Intermediates
and Specialty Chemicals
for
At
Submitted to
State Expert Appraisal Committee (SEAC-I), Maharashtra
September 2020
Proposed Manufacturing Unit of Pharmaceuticals Intermediates and Specialty Chemicals 2020
TABLE OF CONTENTS
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LIST OF FIGURES
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LIST OF FIGURES
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ABBREVIATIONS
SH State Highway
NH National Highway
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LIST OF ANNEXURES
Annexure 1 - Master Layout
Annexure 2 - PNID Diagrams of all the products
Annexure 3 - Equipment list
Annexure 4 - Possession Receipt
Annexure 5 - Contour Plan
Annexure 6 - Toposheet Map
Annexure 7 - Acknowledgment of CER activities submitted to Collector, Nagpur District
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Executive Summary
M/s. Navitus Chemicals Private Limited (henceforth referred as “NCPL” in this report) has been
conceptualized to manufacture an array of divergent path-breaking intermediates valued in
domain of Communicable diseases vertical as well as non-Communicable diseases vertical. The
proposed manufacturing facility is located at plot No. A-24/100 & A-24/105, Umred Industrial
Area, Dist. Nagpur, Maharashtra has a plot area of 7981 sq.m. As per EIA notification 2006, its
amendments and S.O. 1223 (E), dated 27th March 2020, the aforesaid project falls under 5f
Category B2.The industry has proposed 26 products with proposed annual capacity of 1850
MTPA. NCPL will not limit itself only in pharmaceuticals sector but also manufacture Speciality
chemicals. In these sectors there is a huge demand for intermediates, which at present is fulfilled
by China. NCPL proposes manufacturing of Oxirane and intermediates used in manufacturing of
drugs important in COVID-19 treatment in immediate pipeline. Oxirane is used in manufacturing
of Lumefantrine intermediate. 4,7-Dichloroquinoline is a starting material of Chloroquine &
Hydroxychloroquine, 5-Chloro-2-Pentanone is a side chain material of Chloroquine &
Hydroxychloroquine and 6-Bromo-3-hydroxy pyrazine-2-carboxamide, an important starting
material of Favipiravir-Antiviral currently used in the treatment of COVID-19.
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Navitus Chemicals Private Ltd. (NCPL) has been conceptualized to manufacture an array of
divergent path-breaking intermediates valued in domain of Communicable diseases vertical as
well as non-Communicable diseases vertical.
The communicable diseases are major public health problem in the country. To control and
eliminate various communicable diseases specific national health programmes are being
implemented in the country. The National Vector Borne Disease Control Programme
(NVBDCP) is being implemented for control of Malaria, Dengue, Chikungunya and Japanese
Encephalitis (JE) and elimination of Kala-azar and Lymphatic Filariasis. Around 1 million cases
of malaria are being reported annually through public health system. 25,000-75,000 confirmed
dengue cases are being reported under NVBDCP annually in the country with case fatality ratio
of < 0.5%. Among the six diseases, Malaria, Kala-azar and Filaria have specific drug for
treatment. Even after achieving elimination of Kala-azar and filaria, drugs for these diseases will
continuously be required till eradication is being achieved. Malaria is outbreak- prone disease
and continuous availability of drug is to be ensured. There should be mechanism for sustenance
of production and uninterrupted supply of quality drugs. Outside India all African nations are
major consumers of anti-Malarial drugs.
7-Ethyl tryptophol is the starting material used in the manufacturing of Etodolac, which is used
as anti-inflammatory. 4-n- butyl resorcinol is an important compound used in skin whitening
creams. To name a few companies like Lupin, IPCA, Emcure are manufacturing Etodolac. These
companies are totally dependent on Chinese suppliers for 7-Ethyl tryptophol. The aim of the
company is to replace these Chinese suppliers by providing quality material at competitive price.
NCPL will not limit itself only in pharmaceuticals sector but also manufacture speciality
chemicals. In these sectors there is a huge demand for intermediates, which at present is fulfilled
by China. NCPL proposes manufacturing of Oxirane and intermediates used in manufacturing of
drugs important in COVID-19 treatment in immediate pipeline. Oxirane is used in Lumefantrine
intermediate.4,7-Dichloroquinoline is a starting material of Chloroquine & Hydroxychloroquine,
5-Chloro-2-Pentanone is a side chain material of Chloroquine & Hydroxychloroquine and 6-
Bromo-3-hydroxy pyrazine-2-carboxamide, an important starting material of Favipiravir-
Antiviral currently used in the trials for the treatment of COVID-19.
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production capacity of 288 MTPA. The list of products and annual production capacity are listed
in Table 2-2.
The core team consists of NCPL consists of Mr. Shailesh Dhabekar, Mr. Girish Lad, Mr. Sameer
Bhalerao and Mr. Shyam Titirmare. The team has vast experience in chemical industry. Their
roles and responsibilities and profiles are presented in Table 1-1 and Table 1-2 below.
Table 1-1: Role and Responsibility of Core Team Members
Sr. No Name Designation Responsibility
1. Shailesh Dhabekar Director 1 Liasoning & negotiation with manufacturers and
vendors
Finance Management
Human Resource Management.
2. Girish Lad Director 2 Marketing and Supply chain management
3. Sameer Bhalerao Director 3 Product Management
Scientific Communication.
Human Resource Management.
4. ShyamTitirmare Director 4 Technical Planning & Execution of project related
policies.
Trouble shooting in day to day activities.
Key point of communication between management &
employees.
Table 1-2: Profile of Core Team Members
Profile of Core Team Members
Shailesh Dhabekar- Director 1
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1.3 Need for the project and its importance to the country and our region
Considering current market situation and demand amid COVID-19, NCPL proposes
manufacturing of following products along with Oxirane (used in Lumefantrine intermediate) in
immediate pipeline:
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2. Project Description
The proposed project is a new project it does not include any interlinked and interdependent
projects.
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Nagpur
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Table 2-1: Physical and Social Infrastructure around the Project Site
Sr. No. Particulars Details (Aerial distance)
1. Project Location Umred Industrial Area
2. Nearest Highway SH 258- Wardha- Samudrapur-Umred Highway - 0.31 km
NH 247 - 1.67 km
3. Nearest city/town Umred
4. Nearest Fire Station Umred Fire Station -3.3 km
5. Nearest Airport Nagpur Airport – 39.41 km
6. Nearest Railway Umred Railway Station- 2.38 km
Station
7. Water body Hirvatalav - 2.40 km NE
Pandherbodi Talav- 3.67 km SW
Makardhokda Dam and Reservoir - 11.08 km NW
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4. 5-Chloro-2-Pentanone 72 0.74
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7. (2S,3S)-1,2-Epoxy-3-(Boc-amino)-4- 48 0.38
phenylbutane
2-(3-chloropropyl)-2,5,5-trimethyl-1,3- 24 0.176
14.
dioxane
23. 60 0.24
Tyramine HCl
6-Bromo-3-hydroxy pyrazine-2- 36 0.83
24.
carboxamide
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1) 2-(2,7-dichloro-9-H-fluoren-4-yl)oxirane:
a. Brief Process
Fluorene is chlorinated using Chlorine gas & a catalyst. DMF is used as solvent. The obtained
2,7-Dichlorofluorene is reacted with Chloroacetyl chloride in presence of Aluminum chloride.
The acetylated product is then reduced with Sodium borohydride & treated with sodium
hydroxide to get the product. Final material is isolated from Methanol.
b. Route of Synthesis
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2) 7-Ethyl trytophol:
a. Brief Process:
2-Ethyl aniline is diazotized with Sodium nitrite & HCl in aqueous medium. The diazotized mass
is then reduced to get 2-Ethyl phenyl hydrazine HCl. This product is then treated with 2-3-
Dihydrofuran to get 7-Ethyl trytophol.
b. Route of Synthesis
c. Mole Balance
No. of Input No. of Output
Input moles wt Output moles wt
7-Ethyl Phenyl Hydrazine
HCl 1 172.5 7-Ethyl tryptophol 1 189
Ammonium
2,3 - Dihydrofuran 1 70 Chloride 53.5
Total 242.5 Total 242.5
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d. Material Balance
Input kg Output kg
2-Ethyl aniline 500.0 7-Ethyl tryptophol 652
Toluene 1200.0 Recovered Toluene 1158 (96.5%)
HCl 1000.0 Organic waste 122
NaNO2 308.0 Effluent 3172
Reducing agent 563.0 Handling and Process loss 274
2,3-Dihydrofuran 300.0
Catalyst 7.0
Water 1500.0
Total 5378.0 Total 5378.0
3) 4,7-Dichloroquinoline:
a. Brief Process:
3-Chloroaniline is heated with Methyl methoxy-methlyene malonate to get intermediate which is
further heated & treated with Sodium hydroxide to get Sodium salt of 7-Chloro-4-hydroxy-3-
quinoline carboxylic acid. This salt is heated for de-carboxylation to get 7-Chloro-3-hydroxy
quinoline. The hydroxyl group is converted to Chloro by using Phosphorus oxychloride to get
4,7-Dichloroquinoline.
b. Route of Synthesis
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c. Mole Balance
No. of No. of Output
Input moles Input wt Output moles wt
m-Chloroaniline 4,7-Dichloro
1 127.5 quinoline 1 198
Methyl methoxy
methylene malonate 1 174 Methanol 3 96
Phosphorus Oxychloride 1 51 Carbon dioxide 1 44
Sodium
HCl 2 73 phosphate 1 54
Sodium
Sodium hydroxide 3 120 Chloride 2 117
water 2 36
Total 545.5 Total 545
d. Material Balance
Input kg Output Kg
m-Chloroaniline 500.00 4,7-Dichloro quinoline 699
Methyl methoxy methylene malonate 716.00 Organic waste 92
Diphenyl ether 1500.00 Carbon dioxide evolved 172.55
Caustic solution 50 % 790.00 Recovered Methanol 376
Conc HCl 35 % 900.00 1476
Recovered Diphenyl ether (98%)
POCl3 300.00 Aq. layer to ETP 4678
Water 3000.00 1168
Recovered MCB (97%)
MCB 1200.00 Handling and Process loss 244.45
Total 8906 Total 8906
4) 5-Chloro-2-pentanone:
a. Brief Process:
2-Acetyl butyrolactone is heated in presence of Hydrochloric acid. Carbon dioxide gas is
evolved during heating to give 5-Chloro-2-pentanone.
b. Route of Synthesis
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c. Mole Balance
Input Output
Input No. of moles wt Output No. of moles wt
2-Acetyl 1 128 5-Chloro-2- 1 120.5
butyrolactone pentanone
Hydrochloric acid 1 36.5 Carbon dioxide 1 44
Total 164.5 Total 164.5
d. Material Balance
Input kg Output kg
2-Acetyl butyrolactone 750.00 5-Chloro-2-pentanone 628.5
Conc. HCl 35% 600.00 Organic waste 77
Carbon dioxide evolved 257.8
Effluent to ETP 370
Handling and process loss 16.7
Total 1350 Total 1350
5) 4-n-Butyl resorcinol:
a. Brief Process
Resorcinol is reacted with Butyryl chloride in presence of a catalyst to get acylated product. This
product is then reduced using Hydrazine hydrate to get 4-n-Butyl resorcinol.
b. Route of Synthesis
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c. Mole Balance
Input No. of moles Input wt Output No. of moles Output wt
4-n-butyl
Resorcinol 1 110 resorcinol 1 166
n-Butyryl
chloride 1 106.5 HCl 1 36.5
Hydrazine 1 32 Nitrogen 1 28
Water 1 18
Total 248.5 Total 248.5
d. Material Balance
Input kg Output kg
Resorcinol 200.00 4-n-butyl resorcinol 275
MDC 1200.00 Recovered MDC 1153 (96%)
n-Butyryl chloride 200.00 Recovered catalyst 50
Catalyst 50.00 Evaporator feed 901
Water 600.00 Organic waste 30
80 % Hydrazine 77.00 Handling and Process loss 68
Caustic lye 150.00
Total 2477 Total 2477
6) Cetyl ethyldimonium ethosulphate:
a. Brief Process
Cetyl alcohol is sulphonated by using p-Toluene sulphonyl chloride. This intermediate is reacted
with Di-methylamine to get Cetyl di-methylamine. Finally diethyl sulphate is reacted with Cetyl
di-methylamine to get Cetyl ethyldimonium ethosulphate.
b. Route of Synthesis
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c. Mole Balance
Input No. of Output
Input No. of moles wt Output moles wt
Cetyl ethyl dimonium
Cetyl alcohol 1 242.5 ethosulphate 1 423.7
p-Toluene p-Toluene Sulfonic acid
Sulfonyl Chloride 1 190.50 dimethyl amine salt 1 217
Dimethyl amine 2 90 HCl 1 36.5
Diethyl Sulphate 1 154
Total 677 Total 677
d. Material Balance
Input kg Output kg
Cetyl alcohol 300.0 Cetyl ethyl dimonium ethosulphate 483
1148
MDC 1200.0 Recovered MDC (95.67%)
p-Toluene sulfonyl chloride 250.0 Recovered IPA 1168 (97.3%)
Sodium bicarbonate 115.0 Evaporator feed 1280
Water 900.0 Organic waste 53
Catalyst 15.0 Handling and process loss 191
Diethyl sulphate 190.0
IPA 1200.0
Dimethyl amine 40 % 153.0
Total 4323.0 Total 4323.0
7) (2S, 3S)-1,2-Epoxy-3-(Boc-amino)-4-phenylbutane:
a. Brief Process:
Chloroketone is reacted with Sodium borohydride in presence of a catalyst to get Chloro alcohol
which is further cyclised using Sodium hydroxide to get (2S,3S)-1,2-Epoxy-3-(Boc-amino)-4-
phenylbutane.
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b. Mole Balance
No. of Input No. of Output
Input moles wt Output moles wt
(3S)-3-(tertbutoxy (2S,3S)-1,2-epoxy-
carbonyl)-amino-1- 3-(BOC-amino)4-
chloro-4-phenyl butane 1 297.5 Phenyl butane 1 263
Hydrogen
(from NaBH4) 1 2 NaCl 1 58.5
NaOH 1 40 Water 1 18
Total 339.5 Total 339.5
c. Material Balance
Input kg Output Kg
Chloroketone 500.00 (2S,3S)-1,2-epoxy-3-(BOC- 406
amino)4-Phenyl butane
NaBH4 31.70 Recovered MDC 2401
(96.04%)
MDC 2500.00 Recovered Methanol 1357.9
(96.99%)
NaOH 50 % 135.00 Recovered catalyst S 1.50
Methanol 1400.00 Evaporator feed 732
Water 600.00 Organic waste 38
Catalyst S 1.50 Process and Handling loss 231.8
Total 5168.2 Total 5168.2
8) (2R, 3S)-1,2-Epoxy-3-(Boc-amino)-4-phenylbutane:
a. Brief Process
Chloroketone is reacted with Sodium borohydride in presence of a catalyst to get Chloro alcohol
which is further cyclised using Sodium hydroxide to get (2R,3S)-1,2-Epoxy-3-(Boc-amino)-4-
phenylbutane.
b. Route of Synthesis
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c. Mole Balance
No. of No. of Output
Input moles Input wt Output moles wt
(3S)-3-(tertbutoxy (2R,3S)-1,2-epoxy-3-
carbonyl)-amino-1- (BOC-amino) 4-
chloro-4-phenyl butane 1 297.5 Phenyl butane 1 263
Hydrogen
(from NaBH4) 1 2 NaCl 1 58.5
NaOH 1 40 Water 1 18
Total 339.5 Total 339.5
d. Material Balance
Input kg Output Kg
Chloroketone 500.00 (2R, 3S)-1,2-Epoxy-3-(Boc-
amino)-4-phenylbutane 404
NaBH4 31.70 1361
Recovered IPA (97.21%)
MDC 2500.00 2397
Recovered MDC (95.88%)
NaOH 50 % 135.00 Recovered Catalyst 1.5
IPA 1400.00 Evaporator feed 726
Water 600.00 Organic waste 40
Catalyst R 1.50 Process and Handling loss 241.7
Total 5168.2 Total 5168.2
9) tert-Butyl (2S,3R)-3-hydroxy-4-(N-isobutyl-4-nitrophenylsulfonamido)-1-phenylbutan-2-
ylcarbamate(BOC-nitro):
a. Brief Process
BOC-Amino alcohol is reacted with p-Nitrobenzene sulphonyl chloride using MDC as solvent &
Sodium bicarbonate as base to get the product.
b. Route of Synthesis
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c. Mole Balance
Input No. of moles Input wt Output No. of moles Output wt
BOC-Amine 1 336 BOC-nitro 1 521
p-Nitrobenzene Hydrogen
1 221.5 1 36.5
sulfonyl chloride chloride
Total input 557.5 Total Output 557.5
d. Material Balance
Input kg Output Kg
Boc-Amine 400.00 BOC-nitro 590
p-NO2 benzene sulfonyl chloride 255.00 Recovered MDC 2880 (96.6%)
Sodium Carbonate 130.00 Recovered Methanol 1149 (95.75%)
MDC 3000.00 Effluent 1166
Water 1000.00 Organic waste 41
Methanol 1200.00 Handling and Process loss 159
Total 5985.00 Total 5985.00
10) 2-Carboxy benzaldehyde:
a. Brief Process
Phthalide is reacted with Dichloro hydantoin in presence of a catalyst & then it is hydrolyzed
with water to get 2-Carboxy benzaldehyde.
b. Route of Synthesis
c. Mole Balance
Input No. of moles Input wt Output No. of moles Output wt
Phthalide 1 134 2-Carboxy benzaldehyde 1 150
Water 1 18 Hydrogen Bromide 1 81
DBDMH 0.5 143 DMH 0.5 64
Total 295 Total 295
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d. Material Balance
Input Kg Output Kg
Phthalide 800.00 2-Carboxy benzaldehyde 806
1,3-Dibromo,5-5 dimethyl hydantoin 900.00 Recovered MCB 3125 (97.66%)
MCB 3200.00 Evaporator feed 3150
Catalyst 4.00 Organic waste 95
Water 2500.00 Handling and Process loss 228
Total 7404 Total 7404
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c. Mole Balance
No. of Input No. of Output
Input moles wt Output moles wt
2-Phenylethyl methyl 4-(2-methoxy-
ether 1 136 ethyl)phenol 1 152
Acetyl chloride 1 78.5 Methyl acetate 1 74
Methanol 1 32 Hydrogen chloride gas 1 36.5
Hydrogen Peroxide 1 34 water 1 18
Total 280.5 Total 280.5
d. Material Balance
Input Kg Output Kg
2-Phenylethyl methyl ether 1250.0 4-(2-methoxy-ethyl)phenol 1240
Acetyl chloride 758.0 2866
Recovered MDC (95.53%)
MDC 3000.0 Recovered catalyst 125
Catalyst 125.0 Effluent 5848
H2O2 50 % 656.0 Organic waste 165
Methanol 400.0 Handling and Process loss 218
Caustic lye 50 % 773.0
Total 10462 Total 10462
12) Cyclen:
a. Brief Process:
Triethylene tetramine is reacted with Glyoxal to get imine as intermediate. In-situ this imine is
reduced with Sodium borohydride to get Cyclen.
b. Route of Synthesis
c. Mole Balance
Input No. of moles Input wt Output No. of moles Output wt
Triethylene tetramine 1 146 Cyclene 1 172
Glyoxal 1 58 Water 2 18
Hydrogen from NaBH4 1 4
Total 208 Total 208
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d. Material Balance
Input Kg Output Kg
Triethylene tetramine 200.00 Cyclene 219
40 % Glyoxal 220.00 Organic waste 16
Sodium borohydride 26.30 Recovered MCB 487 (97.4%)
MCB 500.00 Water from Glyoxal &
reaction 297
Water 100.00 Handling and Process loss 27.3
Total 1046.3 Total 1046.3
c. Mole Balance
No. of No. of Output
Input moles Input wt Output moles wt
Phenyl hydrazine 4-Hydroxy
hydrochloride 1 144.5 carbazole 1 183
Ammonium
1,3-Cyclohexanedione 1 112 Chloride 1 53.5
Water 1 18
Hydrogen
(absorbed by
aromatizing agent) 1 2
Total 256.5 Total 256.5
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d. Material Balance
Input kg Output Kg
Phenyl hydrazine HCl 600.00 4-Hydroxy Carbazole 691.5
1,3-Cyclohexanedione 480.00 Recovered n-Butanol 1228.8 (96%)
n-Butanol 1280.00 Effluent 1526
Catalyst 30.00 Organic waste 64
Water 1200.00 Handling and Process loss 79.7
Total 3590 Total 3590
14) 7-Chloroquinaldine:
a. Brief Process:
3-Chloroaniline & paraldehyde are reacted under reflux conditions in presence of Hydrochloric
acid & n-Butanol. Aqueous layer is separated & Sodium hydroxide is added to isolate 7-
Chloroquinaldine.
b. Route of Synthesis
c. Mole Balance
No. of No. of Output
Input moles Input wt Output moles wt
3-
Chloroaniline 1 127.50 7-Chloroquinaldine 1 177.5
Paraldehyde 0.66 88 Water 3 54
HCl 1 36.5 NaCl 1 58.5
Hydrogen (absorbed
NaOH 1 40 by aromatizing agent) 1 2
Total 292 Total 292
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d. Material Balance
Input kg Output Kg
3-Chloroaniline 700 7-Chloroquinaldine 782
Paraldehyde 760 Recovered n-Butanol 576 (96%)
n-Butanol 600.00 Evaporator feed 2696
Con HCl 800.00 Organic waste 210
Water 1000.00 Handling and Process loss 156
Caustic lye 560.00
Total 4420 Total 4420
15) 2-(3-chloropropyl)-2,5,5-trimethyl-1,3-dioxane:
a. Brief Process:
5-Chloro pentanone & Neopentyl glycol are reacted in presence of a catalyst &Toluene as
solvent. Water is removed to get the product.
b. Route of Synthesis
c. Mole Balance
No. of Input No. of Output
Input moles wt Output moles wt
2-(3-chloropropyl)-
5-Chloro-2- 2,5,5-
pentanone 1 120.5 trimethyl-1,3-dioxane 1 202.5
Neopentyl glycol 1 104 Water 1 18
Total 224.5 Total 224.5
d. Material Balance
Input kg Output kg
5-Chloro-2-pentanone 2-(3-chloropropyl)-2,5,5-
250.00 400
trimethyl-1,3-dioxane
Toluene 500.00 Organic waste 35
Neopentyl glycol 482
225.00
Recovered Toluene (96.4%)
Catalyst Water generated goes to
2.50 37
evaporator
Handling and Process loss 23.5
Total 977.50 Total 977.50
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c. Mole Balance
No. of Input No. of Output
Input moles wt Output moles wt
3-Ethyl-4- N-{2-[4-(aminosulfonyl)
methyl-2-oxo- phenyl]ethyl}-3-ethy;-4-
1 125.00 1 351
pyrroline methyl-2-oxo-2,5-dihydro-
1H-pyrrole-1-carboxamide
2-Phenyl ethyl
1 147.00 1 18
isocyanate Water
Chlorosulphonic
1 116.50 1 36.5
acid HCl
Ammonia 1 17
Total 405.5 Total 405.5
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d. Material Balance
Input kg Output Kg
3-Ethyl-4-methyl-2-oxo- 200.00 N-[2-[4-(Aminosulfonyl) phenyl]
pyrroline ethyl]-3-ethyl-2,5-dihydro-4-
methyl-2-oxo-1H-pyrrole-1-
carboxamide 615
2-Phenyl ethyl isocyanate 245.00 Organic waste 103
Chlorosulphonic acid 410.00 774
Recovered IPA (96.75%)
Ammonia 25 % solution 550.00 1922
Recovered MDC (96.1%)
IPA 800.00 Evaporator feed 2532
MDC 2000.00 Handling and process loss 59
Water 1800.00
Total 6005.00 Total 6005.00
17) (S)-2-(Aminomethyl)-1-ethylpyrrolidine:
a. Brief Process
L-Proline is reacted with Diethyl sulphate in presence of a base to get N-Ethyl –L-proline ethyl
ester. This ester is then reduced to alcohol by using Sodium borohydride. The alcohol product is
treated with Methane sulphonyl chloride & then with ammonia to get (S)-2-(Aminomethyl)-1-
ethylpyrrolidine.
b. Route of Synthesis
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c. Mole Balance
No. of Output
Input No. of moles Input wt Output moles wt
(S)-2-Aminomethyl-1-
L-Proline 1 115 ethylpyrrolidine 1 128
Diethyl Sulfate 1 154 Ethanol 1 46
Ammonia 1 17 Sodium Sulphate 1 142
Hydrogen (from
reducing agent) 2 4 Water 3 54
NaOH 2 80
Total 370 Total 370
d. Material Balance
Input kg Output Kg
L-Proline 300.0 (S)-2-Aminomethyl-1-ethylpyrrolidine 297
Diethyl sulphate 202.0 Organic waste 38.4
Water 1600.0 Effluent 1966
Caustic lye 210.0 In-organic salts 272
NaBH4 48.6 Handling and process loss 9.2
NH3 25 % 222.0
Total 2582.6 Total 2582.6
18) 2-Cyano phenol:
a. Brief Process:
Salicylic acid is converted to its ammonium salt by using Ammonia & Diphenyl ether as solvent.
Catalyst is added & mass is heated. Dehydration takes place to get 2-Cyano phenol.
b. Route of Synthesis
c. Mole Balance
Input No. of moles Input wt Output No. of moles Output wt
Salicylic acid 1 138 2-Cyano phenol 1 119
Ammonia 1 17 Water 2 18
Total 155 Total 155
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d. Material Balance
Input kg Output kg
Salicylic acid 1250.00 2-Cyano phenol 1004.00
Ammonia 155.00 Organic waste 232.00
Diphenyl ether 4000.00 Recovered Diphenyl ether 3880 (97%)
Catalyst 125.00 Water generated sent to evaporator 326
Handling and process loss 88
Total 5530.00 Total 5530.00
19) 2-Cyclohexen-1-one:
a. Brief Process:
Cyclohexanone is reacted with 1,3-Dibromo-5,5-di-methyl hydantoin(DBDMH) in presence of
Monoethylene glycol. The intermediate obtained is treated with alkali & further deprotection of
ethylene glycol is carried out to get 2-Cyclohexen-1-one.
b. Route of Synthesis
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c. Mole Balance
No. of
Input moles Input wt Output No. of moles Output wt
2-Cyclohexen-
Cyclohexanone 1 98 1-one 1 96
DBDMH 0.5 143 DMH 0.5 64
Sodium
Hydroxide 1 40 NaBr 1 103
MEG 1 62 Water 1 18
MEG 1 62
Total 343 Total 343
d. Material Balance
Input Kg Output Kg
Cyclohexanone 1250.0 2-Cyclohexen-1-one 1028.0
DBDMH 1850.0 Organic waste 198.0
MEG 800.0 Recovered DBDMH 828.0
PTSA 60.0 Recovered MEG 776.0 (97%)
Caustic lye 50 % 1024.0 Recovered Ethyl acetate 816.0 (96%)
Ethyl acetate 850.0 Evaporator feed 5110.0
Water 3200.0 Handling and Process loss 278
Total 9034.0 Total 9034.00
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c. Mole Balance
No. of Input No. of Output
Input moles wt Output moles wt
4-methoxy 4-Methoxy
Aniline 1 123 phenylhydrazine HCl 1 174.5
NaNO2 1 69 NaCl 1 58.5
HCl 1 36.5 Water 2 36
Hydrogen from
reducing agent 2 4
Total 269 Total 269
d. Material Balance
Input Kg Output kg
4-Methoxy aniline 400.0 4-Methoxy phenylhydrazine HCl 516
NaNO2 231.0 Organic waste 58
HCl 800.0 Recovered Butanol 781 (97.63%)
Butanol 800.0 Effluent to ETP 4046
Water 3000.0 Handling and Process loss 225
Reducing agent 425.0
Total 5656 Total 5656
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c. Mole Balance
No. of Input No. of Output
Input moles wt Output moles wt
2-Amino-6-Methoxy
4-methoxy Aniline 1 123 benzothiazole 1 180
Ammonium
thiocyanate 1 76.1 Ammonium Chloride 1 53.5
Chlorine 1 70.9 Hydrogen chloride 1 36.5
Total 270 Total 270
d. Material Balance
Input kg Output Kg
p-Anisidine 600.0 2-Amino-6-methoxy benzothiazole 816
Sodium thiocyanate 415.0 Organic waste 65.5
MDC 4000.0 3840.0
Recovered MDC (96%)
Chlorine 347.0 Evaporator feed 3722
NH3 25 % 335.0 Handling and Process loss 253.5
H2O 3000.0
Total 8697.0 Total 8697.0
22) Tyramine HCl:
a. Brief Process
Tyramine free base is taken in Isopropyl alcohol. HCl is added to the reaction mass to get
Tyramine HCl.
b. Route of Synthesis
c. Mole Balance
Input No. of moles Input wt Output No. of moles Output wt
Tyramine 1 137 Tyramine HCl 1 173.5
HCl 1 36.5
Total 173.5 Total 173.5
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d. Material Balance
Input kg Output kg
Tyramine 600.00 Tyramine Hydrochloride 737.5
1958
HCl 165.00 Recovered IPA (97.9%)
IPA 2000.00 Organic waste 34.5
Handling and Process loss 35
Total Input 2765 Total output 2765
23) 8-Nitroquinaldine:
a. Brief Process:
2-Nitroaniline is reacted with Paraldehyde in presence of a Hydrochloric acid& a catalyst. To
isolate the product the acidity is neutralized with caustic solution.
b. Route of Synthesis
c. Mole Balance
Input No. of moles Input wt Output No. of moles Output wt
2-Nitro aniline 1 138 8-Nitroquinaldine 1 188
Paraldehyde 0.66 132 Water 3 56
HCl 1 36.5 Sodium Chloride 1 58.5
NaOH 1 40
Total 302.5 Total 302.5
d. Material Balance
Input kg Output kg
2-Nitro aniline 500.0 8-Nitroquinaldine 501.0
Paraldehyde 458.0 Organic waste 157.0
35 % HCl 800.0 Recovered MCB 486.0 (97.2%)
Water 1400.0 Evaporator feed 2304.0
Water recovered during
Catalyst 50.0 241.0
drying of the product
Caustic lye 50 % 490.0 Inorganic salts 336.0
MCB 500.0 Handling and Process loss 170
Total 4198.0 Total 4198.0
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c. Mole Balance
No. of Input No. of Output
Input moles wt Output moles wt
2-Amino 1 117 6-Bromo-3-hydroxy- 1 218
propanediamid pyrazine-2-carboxamide
e
Glyoxal 1 58 Hydrogen bromide 1 80.9
Bromine 1 159.8 Water 2 36
Total input 334.8 Total Output 334.9
d. Material Balance
Input kg Output kg
2-Amino propane diamide 200.0 6-Bromo-3-hydroxy
pyrazine-2-carboxamide 302.0
40 % Glyoxal 250.0 Organic waste 84.0
Caustic lye 50 % 140.0 Recovered Acetonitrile 867.0 (96.33%)
Bromine 275.0 Evaporator feed 1596.0
Acetonitrile 900.0 Handling and Process
loss 116
Water 1200.0
Total 2965.0 Total 2965.0
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c. Mole Balance
No. of No. of Output
Input moles Input wt Output moles wt
2,4- dichloro 1 191 5-Sulfamoyl-2,4- 1 270
benzoic acid dichlorobenzoic acid
Chlorosulfuric 1 233 HCl 1 36.5
acid
Ammonia 2 17 H2SO4 1 98
Ammonium Chloride 1 53.5
Total input 458 Total Output 458
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d. Material Balance
Input kg Output Kg
2,4-Dichloro benzoic acid 5-Sulfamoyl-2,4-Dichloro
500.0 615.0
benzoic acid
Chlorosulphonic acid 645.0 Organic waste 103.0
MDC 2500.0 Recovered MDC 2389.0 (95.56%)
Ammonia 1952.0
800.0
Recovered IPA (97.6%)
IPA 2000.0 Evaporator feed 2458.0
Water 1400.0 Handling and Process loss 328
Total 7845.0 Total 7845.0
26) 4-Chloro benzaldehyde
a. Brief Process
4-Chloro toluene is side chain chlorinated in presence of a catalyst. The side chain chlorinated
product is hydrolyzed & extracted in Chlorobenzene & distilled to get pure product
b. Route of Synthesis
c. Mole Balance
No. of Input No. of Output
Input moles wt Output moles wt
p-chloro p-chloro
Toluene 1 126.5 benzaldehyde 1 140.5
Water 2 36 HCl 4 146
Chlorine 2 142 water 1 18
Total 304.5 Total 304.5
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d. Material Balance
Input kg Output Kg
p-Chlorotoluene 1250.0 4-Chloro benzaldehyde 1638
Chlorine gas 1420.0 HCl gas 730.0
Catalyst 30.0 Recovered MCB 1168 (97.33%)
H2SO4 1000.0 Effluent 5022
Water 4000.0 Organic waste 342.0
MCB 1200.0
Total 8900.0 Total 8900.0
Material balance:
The data submitted is from lab batches. The project proponent is confident of achieving better
recoveries of solvents in plant, as the processes are in closed loop & reactors will be equipped
with primary & secondary condensers. Low boiling solvents recovery will have secondary
condensers with -8°C brine solutions which will help to improve recovery percentage resulting
in better material balance.
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2. (2S,3S)-1,2-Epoxy-3-(Boc-amino)-4-phenylbutane
(3S)-3-(tert- Solid. packed in 25 Road
1.0 ton
butoxycarbonyl) amino- Kg bags
a.
1-chloro-4-
phenylbutane
b. Methylene dichloride Liquid. Tanker Road
Solid. 25 Kg bags Road
c. Sodium borohydride placed in 200 Kg
drum
d. Sodium hydroxide Solid. 50 Kg bags Road
3. (2R,3S)-3-(tert-Butoxycarbonyl)amino-1,2-epoxy-4-phenylbutane
(3S)-3-(tert- Solid packed in 25 Road
1.0 ton
butoxycarbonyl) amino- Kg bags
a.
1-chloro-4-
phenylbutane
b. Methylene dichloride Liquid. Tanker Road
Solid. 25 Kg bags Road
c. Sodium borohydride placed in 200 Kg
drum
d. Sodium hydroxide Solid. 50 Kg bags Road
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5. 7-Ethyl trytophol
Liquid. 200 Kg Road
a. 2-Ethyl aniline 2.0 ton
drums
Liquid. Tanker Road
b. Conc. HCl 11.5 ton
Solid. 50 Kg bags Road
c. Sodium nitrite 0.5 ton
Solid. 50 Kg bags Road
d. Reducing agent 2.0 ton
Liquid, 200 Kg Road
e. 2,3-Dihydro furan 2.0 ton
drums
f. Toluene 5.0 ton Liquid. Tanker Road
6. 2-Carboxy benzaldehyde
Solid. 50 Kg bags Road
a. Phthalide 1.0 ton
Solid. 50 Kg bags Road
b. Dibromohydantoin 2.0 ton
Liquid. Tanker Road
c. Chlorobenzene 5.0 ton
7. 4-Hydroxy carbazole
Phenyl hydrazine Solid. 50 Kg bags Road
a. 2.0 ton
Hydrochloride
Solid. 50 Kg bags Road
b. Cyclohexane-1,3-dione 2.0 ton
Liquid. Tanker Road
c. n-Butanol 5.0 ton
Solid. 50 Kg bags Road
d. Aromatizing agent 1.0 ton
8. 4,7-Dichloroquinoline
Liquid. 200 Kg Road
a. 3-Chloroaniline 3.0 ton
drum
Methyl methoxy Liquid. 200 Kg Road
b. 3.0 ton
methylene malonate drum
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12. 5-Chloro-2-pentanone
Liquid. 200 Kg Road
a. 2-Acetylbutyrolactone 3.0 ton
drum
b. Conc HCl Liquid. Tanker Road
13. 4-(2-Methoxyethyl)phenol
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14. Cyclen
Liquid. 200 Kg Road
a. Triethylenetetramine 0.5 ton
drum
Liquid. Tanker Road
b. N-Butanol
Liquid. 200 Kg Road
c. Glyoxal 0.5 ton
drum
Solid. 25 Kg bags Road
0.5 ton
d. Sodium borohydride placed in 200 Kg
drum
15. 2-Cyclohexen-1-one
Liquid. 200 Kg Road
a. Cyclohexanone 5.0 ton
drum
Liquid. Tanker Road
b. Ethyl acetate 5.0 ton
Liquid. 200 Kg Road
c. Monoethylene glycol 3.0 ton
drum
Solid. 25 Kg bags Road
p-Toluene sulphonic 0.5 ton
d. placed in 200 Kg
acid
drum
Solid. 25 kg card- Road
e. DBDMH 5.0 ton
board drum
f. 50 % caustic lye Liquid. Tanker Road
16. 7-Chloroquinaldine
Liquid. 200 Kg Road
a. 3-Chloroaniline 2.0 ton
drum
Liquid. Tanker Road
b. Conc. HCl
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17. 8-Nitroquinaldine
Solid. 25 Kg bags Road
a. 2-Nitroaniline 3.0 ton
Liquid. Tanker Road
b. Conc HCl
18. N-Ethyl-L-prolinamide
Solid. 25 Kg bags Road
a. L-Proline 2.0 ton
Liquid. 40 Kg Road
b. Diethyl sulphate 2.0 ton
Carbouy
Liquid. Tanker Road
c. Caustic lye
200 Lts drum Road
d. Ammonia solution 2.0 ton
Liquid. Tanker Road
e. N-Butanol
Solid. 25 Kg bags Road
2.0 ton
f. Reducing agent placed in 200 Kg
drum
19. Tyramine HCl
Solid. 25 Kg bags Road
a. Tyramine 2.0 ton
Gas. Cylinder Road
b. HCl 0.5 ton
Liquid. Tanker Road
c. IPA 5.0 ton
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2.9 Availability of water its source, Energy/ power requirement and source
During operation of proposed project 66.66 KLD of water will be required for industrial &
domestic purpose. It will be supplied by MIDC pipeline. The total power requirement in the form
of connected load is 600 kVA and demand load of 400 kVA. It will be supplied by MSEDCL.
Solar panels of 20 kVA will be installed which will be used for lights in the entire premises. 300
kVA capacity of DG set will be installed at the site which will be used to run critical processes &
emergency lights. D.G set will be used backup source in case of power failure. Fuel used for
D.G. set will be High speed Diesel with requirement of 200 Liters/day. Detailed water budget is
presented in Table 2-4.
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Particulars/ Waste
Fresh Recycled Loss
Water Water
(KLD) (KLD) (KLD)
Requirement (KLD) Remark
Sewage will be treated in STP.
Domestic 4 0 0.2 3.8 3.8KL will be used for
gardening
5.962 KL goes for aluminates
recovery to registered vendor
Products from Oxirane manufacturing.
25 19.038 5.962 19.038
manufacturing 19.038 KL recovered from
MEE will be directly used in
next batch
2.9KL will be cooling tower
makeup considering 20%
evaporation losses. Once the
Cooling tower 14.5 11.6 1.9 1 TDS crosses 500, the water
will be used for gardening.
1KL per day blow day will be
used for gardening
Hot water System is similar to Thermic
10* 0 10 0
Generator fluid. No losses
Total requirement is 13.16KL
out of which 4.8KL will be
Gardening 13.16 4.8 13.16 0 treated water from STP
(3.8KL) and water blowdown
from Cooling tower (1KL)
Total Water
66.66 35.438 31.225 23.838
requirement
*Once in a lifetime
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2.10 Quantity of wastes to be generated (liquid and solid) and scheme for their
Management/disposal
In operation phase generated solid waste will be segregated. Details of hazardous & non-
hazardous are presented in Table 2-5 and Table 2-6. Hazardous waste is sent to Butibori
CHWTSDF and non-hazardous waste is disposed-off through authorized vendor/
recycler/reprocessor. The liquid waste and trade effluent within the plant will be collected by a
pipe network and treated in ZLD plant. Domestic Sewage waste will be treated in 5 KLD
Sewage Treatment Plant (STP). 0.54 kg per day of treated sludge will be generated from STP.
Table 2-5: Hazardous waste quantification and disposal
Hazardous waste Category Proposed Disposal
(kg/month)
Process waste/Residue 28.1 8100 CHWTSDF
ETP Sludge 35.3 200 CHWTSDF
Discarded drums/Bags 100 CHWTSDF or sale to
33.1
Authorized Recycler
Salts from MEE 37.3 15075 CHWTSDF
Liners 33.1 100 CHWTSDF
Quantification of industrial dry waste like wooden pallets, Glass scrap, Plastic, Paper corrugated
box, Cartons that will be generated in the project is presented in Table 2-6: Details of non-
Hazardous waste. E-Waste of 500 kg/annum will be generated and it will be disposed through
authorized e-waste recyclers. Total excavation material will be about 500 cu.m. It will be used in
refilling.
Table 2-6: Details of non-Hazardous waste
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commissioning of the project activities. However, as per notification S.O. 1223 (E), dated 27th
March 2020, MoEF has directed expeditious disposal of proposal relating to Active
Pharmaceutical Ingredients (API) as Category B2 in light of present situation arising from
COVID-19 outbreak. This OM is valid till 30th September 2020. The proposed project shall be
appraised as Category „B2‟ project.
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3. Site Analysis
3.1 Connectivity
The proposed project site is connected to Nagpur through road and rail linkages. National
Highway NH 247 is at a distance of 1.67 km from project site whereas, SH-258 (Wardha-
Samudrapur-Umred Highway) is at about 300 meters from the project site. Umred has
connectivity to Nagpur district via rail line, which further extends to Bhivapur and Nagbhid. The
nearest airport, Nagpur Airport is about 39.4 km from the project site. The nearest railway
station is Umred situated at2.38 km from the project site.
A-24/100 and A-24/105 7981 sq.mt Private M/s. Navitus Chemicals Pvt. Ltd.
3.3 Topography
The slope of the project site is from north to South direction. The highest and lowest contours
are98.500 m and 96.750 m respectively and the difference is 1.750 m. Contour map is attached
as Annexure-V. The Toposheet map of 1:50,000 scale is attached as Annexure – VI.
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Nagpur).
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Temperature
The temperature generally rises from the beginning of March till June, which is the hottest
month of the year with mean minimum and maximum temperatures of 20.3oC and 36.7oC
respectively. With the onset of monsoons by the end of June, temperature begins to fall. The
drop in day temperature is much more than the drop in night temperature. The night temperature
falls rapidly after the withdrawal of monsoons by mid-September. The month of December is
coolest month with the mean maximum and minimum temperatures being 28.3 oC and 12.1oC
respectively. Sky is generally clear with light surface winds blow from North or North-easterly
direction. The normal minimum temperature is 12.0°C to 14.0°C with slight rise in the mean
daily minimum temperature. The mean maximum temperature is around 29.0°C.
Humidity
Except during monsoon months is generally low throughout the year. During summer season,
humidity is lowest (20.7%). During monsoon months, it goes as high as 80- 90%. The highest
level of humidity (88%) is observed in the month of August.
Rainfall
At Nagpur, the annual rainfall is 1250.7 mm. About 60 to 70 % of the annual rainfall is reviewed
in the monsoon months. The rain in Nagpur is heavily dominated by the south-westerly monsoon
winds. Precipitation in form of rain is received during monsoon months. The number of rainy
days in a year is about 56.9 at Nagpur.
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4. Planning Brief
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4.5 Amenities/Facilities
Facilities like rest rooms, parking area, first aid and recreation facilities will be provided in the
proposed project. In addition to this D.G set as power back up will be installed. No other
additional facilities are proposed.
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5. Proposed Infrastructure
5.5 Connectivity
The project site is well connected by road and rail to Nagpur city and other localities of Nagpur
district. Due to available internal roads and existing connectivity to other regions of Nagpur
district no additional infrastructure is proposed.
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in septic tank/ soak pit. During operation phase, about 3.6 KLD of domestic sewage will be
generated. It will be treated in STP (Capacity 5 CMD) and treated water will be used for
gardening purpose. Details of STP are provided below and influent and effluent characteristics
are presented in Table 5-1.
The Sewage Treatment plant will consist of following units:
Screen chamber
Raw Sewage Sump
MBBR
Secondary Tube Settler
Sludge Drying Beds
Clarified Water Tank
Pressure Sand Filter
Activated Carbon Filter
Treated water Tank
Screen Chamber
Overflow from septic tank comes to Screen Chamber. Screen Chamber is constructed in R.C.C.
at a level of inlet Sewage shall be provided with a screen. This will remove the floating matter
present in the incoming Sewage like plastics, fibers and any other floating material.
Raw Sewage Sump
This tank serves as the holding tank for the incoming Sewage. The overflow of sewage from
septic tank after passing through septic tank is collected in this tank. This will help in loading the
sewage with a consistent flow and will accommodate the variation in flow during the peak
period. From here it is pumped to the MBBR in require steady rate for the biological process and
reaction. This sump would be constructed in RCC.
Moving Bed Bio Reactor
MBBR unit will be equipped with a grid of piping and air diffusers through which compressed
air is passed and distributed throughout the tank in the form of fine bubbles using diffusers. PVC
fill media in the form of Moving bio carriers will also be provided for the immobilization of the
additional bio mass. The PVC Bio carriers increases the contact period of air and water and helps
in maintaining the MLSS in aeration tank. Here fine bubble flexible EPDM membrane diffusers
will aerate Sewage along with Bio carriers In MMBR the organic impurities will get oxidized
with the help of microbial organism in to inorganic form. For the first run of the plant the
microbial culture is brought from outside and as the culture grows then the sludge from the
settler acts as the culture.
Secondary Tube Settler
A Tube Settler shall be provided for the settlement of fully aerated Sewage from MBBR unit.
The Settling Tank shall be provided with Tube Deck. Settled sludge at the bottom of Tube Setter
will be discharged to sludge drying beds as per operational requirements. This Sludge being fully
mineralized is suitable for the sun drying on
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The project site is located in notified industrial area and developed by MIDC under Government
of Maharashtra for setting up of industries. It does not involve resettlement and rehabilitation.
The manufacturing of proposed products is planned to commence in6 months after obtaining
Environmental Clearance and other necessary authorizations. The capital investment of the
project is INR 1300 Lakhs. The project schedule and project cost are presented in Table 4-1
and Table 7-1 and respectively.
Table 7-1: Project Cost
S No Particulars Amount (In Lakhs)
1. Land acquisition 100
2. Pre-Operative Expenses 55
3. Civil Work 220
4. Machinery* 730
5. QC & PD Lab Equipment 35
6. Commissioning &Pre-operative funds 60
7. EMP (capital cost of pollution 100
control systems)
Total 1300
*ETP cost is included in Plant machinery
In light of the ongoing COVID-19 pandemic, the proposed project plans to manufacture three
intermediates which serve as starting material for manufacture of APIs for COVID-19 treatment.
The project is located in notified industrial area. There will be no change in land use. The
proposed project will be equipped with the pollution control facilities to handle the pollution
load generated due to its proposed operations. Zero Liquid Discharge for effluent treatment will
be provided. D.G. set with acoustic enclosure will be installed. The proposed project will create
job opportunities (Direct & Indirect) by employing 80 nos. of personnel and will create
opportunities for ancillary business in the project area. Corporate Environmental Responsibility
(CER) activities like construction of toilets and installing solar panels at Nagar Parishad School
at Umrer are among many activities that will be undertaken based on Office Memorandum No.
F.No. 22-65/2017-IA.III dated 1stMay 2018 on CER by MoEF. Acknowledgment of CER
77
BE/PFR Navitus/020/04Rev no. 00
Proposed Manufacturing Unit of Pharmaceuticals Intermediates and Specialty Chemicals 2020
activities submitted to Collector, Nagpur District is attached as Annexure 7. The project will
have tax benefit to the country and foreign exchange savings and Revenue generation for
Government of Maharashtra. Thus, the proposed manufacturing unit shall provide opportunities
for employment creation, import reduction, and saving in foreign currency.
78
BE/PFR Navitus/020/04Rev no. 00
ANNEXURE- 1
1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20
G 05 G 05 FSI STATEMENT
GATE
9.0m [29'-6"]
ENTRY
N N
UG RANK (FIRE) = 60 SQ.M 2.63%
6 m WIDE ROAD
7.1m [23'-1"]
((6.0 x 10.0) x 3.5(deep)
TANK FARM
UG TANK (DOMESTIC) = 12 SQ.M 0.52%
P 04
15.3m [49'-11"]
5 x 21m SECURITY ((6.0 x 2.0) x 3.5(deep)
P 05 G 01 CABIN 01
STORE + ADMIN + LAB (G+1) = 1200 SQ.M 15.03%
6 m WIDE ROAD
25.4m [83'-1"]
4 x 5m
3.1m [10']
((40.0 x 15.0) x 2)
M
WASTE MATERIAL STORAGE
TANK FARM = 105 SQ.M 1.31% M
2.5 x 9 m (5.0 x 21.0)
WASTE MATERIAL STORAGE = 22.5 SQ.M 0.28%
18.9m [61'-11"]
DRUM YARD
UG TANK FIRE (2.5 x 9)
6 x 10 x 3.5 m
G 05 7.5 x 9m DRUM YARD = 67.5SQ.M 0.84%
G 07 G 02 (7.5 x 9)
30 M WIDE ROAD
EVAPORATOR (MEE) = 70 SQ.M 0.87%
L L
UG TANK DOMESTIC (10.0 x 7.0)
6 x 2.5 x 3.5 m
54.5m [178'-6"]
CHLORINE SHED = 25 SQ.M 0.31%
(5.0 x 5.0)
7 x 4.5 x 2 m
7 x 4.5 x 2 m
LIFT HOIST = 4 SQ.M 0.05%
ETP 01
ETP 02
EVAPORATOR (2.0 x 2.0)
10 x 7 m
PLANT 01 = 541.5 SQ.M 6.78%
K ((19.0 x 9.5) x3 (G+2) K
6 m WIDE ROAD
6 m WIDE ROAD
CHLORINE G 07
(3.5 x 5.0)
J J
SHED ETP 01 = 31.5 SQ.M 0.39%
5x5m
((7.0 x 4.5) x2 (deep)
PLANT 02 ETP 02 = 31.5 SQ.M 0.39%
19 x 9.5 m
((7.0 x 4.5) x2 (deep)
P 02 ETP 03 = 31.5 SQ.M 0.39%
6 m WIDE ROAD 6 m WIDE ROAD ((7.0 x 4.5) x2 (deep)
I UTILITY ROOM = 200 SQ.M 2.50% I
G 03
(15.0 x 15.0)
G 03
SECURITY CABIN 02 = 20 SQ.M 0.25%
COMPOUND WALL
115.3m [377'-9"]
+2.4m HIGH
72.3m [236'-8"] (5.0 x 4.0)
TRANSFORMER ROOM = 36 SQ.M 0.45%
6 m WIDE ROAD
(6.0 x 6.0)
H H
G 05
TOTAL F.S.I = 3062 SQ.M 38.37%
PARKING STATEMENT
AREA UNDER PARKING 01 = 122.36 SQ.M
AREA UNDER PARKING 02 = 63.25 SQ.M
59.7m [195'-7"]
E
G 03 GREEN BELT 02 = 38.2 SQ.M E
D UTILITY ROOM D
15 x 15 m
G 05
1.5m [5']
LEGENDS
@ 2.4m FROM GL.
COMPOUND WALL
COMPOUND WALL
33.8m [110'-8"]
+2.4m HIGH
PROJECT :- UMRED INDUSTRIAL AREA, DISTT. NAGPUR.
EXIT
B B
CLIENT :- M/s. NAVITUS CHEMICAL PVT. LTD.
20 M WIDE ROAD
A A
Address E-Mail ID
1st Floor, Junipers - Hemant Building, contact@techture.co.in
Plot No. 2, IT Park, South Ambazari Road, Website
Nagpur - 440011, Maharashtra, India www.techture.co.in
1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20
ANNEXURE- 2
ANNEXURE- 3
Equipment list
Sr. No. Equipment MOC Volume Quantity
Reactors
1 Glass lined MSGLR 3.0 KL 4
2 Glass lined MSGLR 7.0 KL 1
3 Glass lined MSGLR 10.0 KL 1
4 Glass lined MSGLR 1.6 KL 1
5 Stainless steel SSR 7.0 KL 4
6 Stainless steel SSR 5.0 KL 2
7 Stainless steel SSR 3.0 KL 2
8 Stainless steel SSR 1.6 KL 2
Condensor
9 Graphite 15 sqm 3
10 SSR 15 sqm 12
Receiver tank
11 Stirred tank PP 3.0 KL 1
12 Tank HDPE 3.0 KL 5
13 Tank SS 304 3.0 KL 10
14 Tank SS 304 1.0 KL 5
15 Tank SS 304 0.5 KL 6
16 Tank MSGL 7.0 KL 1
17 Tank PP 10 KL 2
18 Tank SS 304 7.0 KL 2
19 Tank SS 304 5.0 KL 2
20 Tankfarm (09) MS 10 KL 8
21 Centrifuge MSRL 48" 2
22 Nutch filter SS 304 2.0 K 2
23 Centrifuge SSR 36" 2
24 ANFD SS 316 5.0 KL 1
25 ANFD SS 316 3.0 KL 1
26 Tray Dryer SS 316 96 tray 1
27 Tray Dryer SS 316 48 tray 1
28 FBD SS 316 100 Kg/Hr 1
29 Pumps 30
30 Ejector system 2
31 Tray Dryer SS 316 96 tray 2
32 Balance 4
33 Boiler 3.0 Ton 1
34 Dowtherm 1.0 Ton 1
35 Cooling tower 500 Tr 1
36 Cooling tower 100 Tr 1
37 Chiller 40 Tr 1
38 Material lift(2 No) 2
39 Evaporator MS Halar 800 Lt/Hr 1
ANNEXURE- 4
ANNEXURE- 5
N 2304780 N 2304780
E 324750
E 324800
E 324850
E 324900
E 324950
E 325000
E 325050
E 324700
LEGENDS
SYMBOL DESCRIPTION SYMBOL DESCRIPTION
N 2304730 N 2304730
TOWARDS
END
N 2304680 N 2304680
N 2304630 N 2304630
NOTES :
1) ALL DIMENSION ARE IN METER
2) GRID SIZE 50m x 50m.
TOWARDS
MIDC AREA
N 2304580 N 2304580 M/s. NAVITUS CHEMICAL PVT. LTD.
UMRED, DISTT. NAGPUR.
imaGIS Engineering
Solutions Pvt. Ltd
E 325050
E 324700
E 324800
E 324850
E 324900
E 324950
E 325000
UMRED INDUSTRIAL AREA, DISTT. NAGPUR.
TOWARDS
MIDC AREA FINAL DRAWING
N 2304530 N 2304530
1 : 500 IESPL / 20-21 / UMS / TPO 160 17/06/20 02
ANNEXURE- 6
79°18′0.00″ 79°24′0.00″
Survey of India Toposheet Indicating Boundary of the Proposed Navitus Chemicals Pvt. Ltd. and 10km radial distance (Study area)
SOI TOPOSHEET MAP
Scale 1:50000
Legend
Navitus Chemicals Pvt. Ltd. Plot Boundary
20°54′0.00″
20°54′0.00″
10km Radial distance (Study Area)
20°48′0.00″
20°48′0.00″
79°18′0.00″ 79°24′0.00″
ANNEXURE- 7