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3-Nitroacetophenone

3-Nitroacetophenone Structure
CAS No.
121-89-1
Chemical Name:
3-Nitroacetophenone
Synonyms
1-(3-NITROPHENYL)ETHANONE;M-NITROACETOPHENONE;(3-nitrophenyl)methylketone;usafma-1;USAF ma-1;AKOS 233-65;AURORA 14018;3-Nitroacetofenon;AKOS BBS-00003220;3-NITROACETOPHENONE
CBNumber:
CB4400448
Molecular Formula:
C8H7NO3
Molecular Weight:
165.15
MOL File:
121-89-1.mol
MSDS File:
SDS
Modify Date:
2024/4/8 17:36:13

3-Nitroacetophenone Properties

Melting point 76-78 °C(lit.)
Boiling point 202 °C(lit.)
Density 1.3450 (rough estimate)
vapor pressure 0.32Pa at 25℃
refractive index 1.5468 (estimate)
Flash point 202°C
storage temp. Sealed in dry,Room Temperature
solubility DMSO (Slightly), Methanol (Slightly)
form Crystalline Powder
color Yellow to yellow-green
Odor Odorless
Water Solubility <0.01 g/100 mL at 20 ºC
BRN 743002
Stability Stable. Incompatible with strong oxidizing agents, strong bases.
InChIKey ARKIFHPFTHVKDT-UHFFFAOYSA-N
LogP 1.42
NIST Chemistry Reference 3-Nitroacetophenone(121-89-1)
EPA Substance Registry System 3-Nitroacetophenone (121-89-1)

SAFETY

Risk and Safety Statements

Symbol(GHS) 
GHS07
Signal word  Warning
Hazard statements  H302-H315-H319-H332-H335
Precautionary statements  P261-P280-P305+P351+P338
Hazard Codes  Xn
Risk Statements  21
Safety Statements  22-24/25
WGK Germany  2
RTECS  AM9625000
TSCA  Yes
HS Code  29147090
Toxicity mouse,LD50,intraperitoneal,200mg/kg (200mg/kg),National Technical Information Service. Vol. AD277-689,
NFPA 704
1
0 0

3-Nitroacetophenone price More Price(10)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich(India) N9381 3′-Nitroacetophenone ReagentPlus?, 99% 121-89-1 100G ₹1880 2022-06-14 Buy
Sigma-Aldrich(India) N9381 3′-Nitroacetophenone ReagentPlus?, 99% 121-89-1 500G ₹5700 2022-06-14 Buy
Sigma-Aldrich(India) 72610 3′-Nitroacetophenone purum, ≥98.0% (GC) 121-89-1 100G ₹2533.05 2022-06-14 Buy
TCI Chemicals (India) N0109 3'-Nitroacetophenone min. 98.0 % 121-89-1 25G ₹2300 2022-05-26 Buy
TCI Chemicals (India) N0109 3'-Nitroacetophenone min. 98.0 % 121-89-1 100G ₹3900 2022-05-26 Buy
Product number Packaging Price Buy
N9381 100G ₹1880 Buy
N9381 500G ₹5700 Buy
72610 100G ₹2533.05 Buy
N0109 25G ₹2300 Buy
N0109 100G ₹3900 Buy

3-Nitroacetophenone Chemical Properties,Uses,Production

Chemical Properties

white to light beige crystalline powder or yellow needle-like crystals. soluble in hot water and ether, slightly soluble in ethanol. can be volatile with water vapor.

Uses

3''-Nitroacetophenone is used as a reactant in the synthesis of fluorine based aminothiazoles with antimicrobial activity.

Preparation

3-Nitroacetophenone is synthesized from acetophenone by nitration.
Synthesis of 3-nitroacetophenone

Production Methods

Acetophenone is carefully dissolved in concentrated sulfuric acid at 0 ℃, and mixed acid is added slowly below 0 ℃. The crude product is precipitated by quenching into ice, filtered, and washed acid free. Purification, mainly from the ortho isomer, is achieved by recrystallization from ethanol with significant lowering of the overall yield to ca. 55 %.

General Description

3-nitroacetophenone is a light beige powder. It is an anthropogenic compound which is used as a synthetic intermediate in the production of dyes and other organic compounds. (NTP, 1992)

Air & Water Reactions

Insoluble in water.

Reactivity Profile

A nitrated ketone. Ketones are reactive with many acids and bases liberating heat and flammable gases (e.g., H2). The amount of heat may be sufficient to start a fire in the unreacted portion of the ketone. Ketones react with reducing agents such as hydrides, alkali metals, and nitrides to produce flammable gas (H2) and heat. Ketones are incompatible with isocyanates, aldehydes, cyanides, peroxides, and anhydrides. They react violently with aldehydes, HNO3, HNO3 + H2O2, and HClO4.

Fire Hazard

Flash point data for 3-Nitroacetophenone are not available, however 3-Nitroacetophenone is probably combustible.

Purification Methods

Distil the ketone in steam and crystallise it from EtOH. [Beilstein 7 IV 656.]

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