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p-Nitroacetophenone

p-Nitroacetophenone

CAS: 100-19-6

Molecular Formula: C8H7NO3

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p-Nitroacetophenone - Names and Identifiers

Name p-Nitroacetophenone
Synonyms AURORA KA-7140
AKOS BBS-00003219
P-NITROACETOPHENONE
p-Nitroacetophenone
4-NITROACETOPHENONE
4-Nitroacetophenone
p-acetylnitrobenzene
4'-Nitroacetophenone
4'-NITROACETOPHENONE
1-(4-nitrophenyl)ethanone
p-nitrophenyl methyl ketone
1-(4-NITROPHENYL)ETHAN-1-ONE
4'-Nitroacetophenone 1-(4-Nitrophenyl)ethan-1-one p-Nitroacetophenone
CAS 100-19-6
EINECS 202-827-4
InChI InChI:1S/C8H7NO3/c1-6(10)7-2-4-8(5-3-7)9(11)12/h2-5H,1H3
InChIKey YQYGPGKTNQNXMH-UHFFFAOYSA-N

p-Nitroacetophenone - Physico-chemical Properties

Molecular FormulaC8H7NO3
Molar Mass165.15
Density1.3450 (rough estimate)
Melting Point75-78°C(lit.)
Boling Point202°C(lit.)
Flash Point201-202°C
Water SolubilityInsoluble in water.
Vapor Presure0.00511mmHg at 25°C
AppearanceCrystalline Powder
ColorYellow
BRN607777
Storage ConditionSealed in dry,Room Temperature
Refractive Index1.5468 (estimate)
Physical and Chemical PropertiesThe pure character is light yellow crystal or needle crystal.
melting point 80~82 ℃
boiling point 202 ℃
solubility soluble in hot ethanol, ether and benzene, insoluble in water.
UseUsed as pharmaceutical chloramphenicol intermediates and dye intermediates

p-Nitroacetophenone - Risk and Safety

Hazard SymbolsXn - Harmful
Harmful
Risk CodesR36 - Irritating to the eyes
R22 - Harmful if swallowed
Safety DescriptionS22 - Do not breathe dust.
S24/25 - Avoid contact with skin and eyes.
WGK Germany3
RTECSAM9627000
HS Code29147090
Hazard NoteHarmful

p-Nitroacetophenone - Upstream Downstream Industry

Raw MaterialsSulfuric acid
Nitric acid
Ethylbenzene
Downstream Productschloroamphenicol

p-Nitroacetophenone - Nature

Open Data Verified Data

pure product is light yellow crystal or needle crystal. The melting point was 80-82 °c. Boiling Point 202 °c. Soluble in hot ethanol, ether and benzene, insoluble in water.

Last Update:2025-06-10 22:55:16

p-Nitroacetophenone - Preparation Method

Open Data Verified Data
  1. ethylbenzene nitrated with mixed acid at 30-35 °c to obtain nitroethylbenzene. After rectification, P-nitroethylbenzene and O-nitroethylbenzene were obtained. P-nitroacetophenone was obtained by the oxidation of p-nitroethylbenzene in the presence of cobalt stearate at 140-150 ℃ and 0.2MPa in air. The reaction product was washed with water, neutralized, centrifuged and dried to obtain a finished product.
  2. p-nitrobenzoyl chloride method.
Last Update:2022-01-01 10:50:42

p-Nitroacetophenone - Safety

Open Data Verified Data
    Toxicity was unknown. Production equipment should be sealed, and operators should wear protective equipment.
  • the container is packed with plastic bags lined with iron or wood barrels. 25k or 50kg net per barrel. Store in a dry, ventilated place.
Last Update:2025-06-10 22:55:16

p-Nitroacetophenone - Reference Information

NIST chemical information information provided by: webbook.nist.gov (external link)
EPA chemical substance information information provided by: ofmpeb.epa.gov (external link)
purpose used as pharmaceutical chloramphenicol intermediate and dye intermediate
organic synthesis intermediate, it is a raw material for the manufacture of medicines such as chloromycetin and chloromycetin.
production method 1. Ethylbenzene Nitration with mixed acid at 30-35 °c to obtain nitration of nitration of nitroethylbenzene. After rectification, P-nitroethylbenzene and O-nitroethylbenzene were obtained. P-nitroethylbenzene is oxidized with air in the presence of the catalyst cobalt stearate at 140-150 °c and a pressure of 0.2MPa to give P-nitroacetophenone. The reaction product was washed with water, neutralized, centrifuged and dried to obtain a finished product. Raw material consumption quota: ethylbenzene 2519kg/t, nitric acid 1535kg/t, sulfuric acid 697kg/t, hydrochloric acid 12kg/t, soda ash 81kg/t, caustic soda 111kg/t, ethanol 100kg/t, methanol 70kg/t. 2. P-nitrobenzoyl chloride method.
Last Update:2024-04-09 19:55:45
p-Nitroacetophenone
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Mobile: +86-13605431940
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View History
p-Nitroacetophenone
Raw Materials for p-Nitroacetophenone
Sulfuric acid
Nitric acid
Ethylbenzene
Downstream Products for p-Nitroacetophenone
chloroamphenicol
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