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2-Nitroaniline

Product Name
2-Nitroaniline
CAS No.
88-74-4
Chemical Name
2-Nitroaniline
Synonyms
ONA;O-NITROANILINE;1-AMINO-2-NITROBENZENE;o-Nitroanilin;O-NITRANILINE;aniline,o-nitro-;Aniline, o-nitro-;2-Nitrobenzenamine;ORTHO-NITROANILINE;Telmisartan Impurity 12
CBNumber
CB6287018
Molecular Formula
C6H6N2O2
Formula Weight
138.12
MOL File
88-74-4.mol
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2-Nitroaniline Property

Melting point:
70-73 °C (lit.)
Boiling point:
284 °C (lit.)
Density 
1,255 g/cm3
vapor pressure 
8.1 at 25 °C (Mabey et al., 1982)
refractive index 
1.6349 (estimate)
Flash point:
168 °C
storage temp. 
Store below +30°C.
solubility 
methanol: 0.1 g/mL, clear
Colour Index 
37025
pka
-0.26(at 25℃)
form 
Crystals or Flakes
color 
Orange to brown
PH
6.1 (10g/l, H2O, 20℃)(slurry)
Water Solubility 
1.1 g/L (20 ºC)
Merck 
14,6582
BRN 
509275
Henry's Law Constant
5.88 x 10-8 atm?m3/mol at 25 °C (thermodynamic method-GC/UV spectrophotometry, Altschuh et al., 1999)
Stability:
Stable. Incompatible with acids, acid chlorides, acid anhydrides, strong oxidizing agents, chloroformates, hexanitroethane.
LogP
1.85 at 25℃
CAS DataBase Reference
88-74-4(CAS DataBase Reference)
NIST Chemistry Reference
o-Nitroaniline(88-74-4)
EPA Substance Registry System
o-Nitroaniline (88-74-4)
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Safety

Hazard Codes 
T,F
Risk Statements 
23/24/25-33-52/53-39/23/24/25-11
Safety Statements 
28-36/37-45-61-28A-16-7
RIDADR 
UN 1661 6.1/PG 2
WGK Germany 
2
RTECS 
BY6650000
8
Autoignition Temperature
521 °C
TSCA 
Yes
HazardClass 
6.1
PackingGroup 
II
HS Code 
29214210
Hazardous Substances Data
88-74-4(Hazardous Substances Data)
Toxicity
LD50 orally in Rabbit: 1600 mg/kg LD50 dermal Rabbit > 7940 mg/kg
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Danger
Hazard statements

H373May cause damage to organs through prolonged or repeated exposure

H412Harmful to aquatic life with long lasting effects

Precautionary statements

P273Avoid release to the environment.

P280Wear protective gloves/protective clothing/eye protection/face protection.

P301+P310IF SWALLOWED: Immediately call a POISON CENTER or doctor/physician.

P314Get medical advice/attention if you feel unwell.

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N-Bromosuccinimide Price

Sigma-Aldrich
Product number
N9780
Product name
2-Nitroaniline
Purity
98%
Packaging
5g
Price
$36.4
Updated
2024/03/01
Sigma-Aldrich
Product number
N9780
Product name
2-Nitroaniline
Purity
98%
Packaging
100g
Price
$103
Updated
2024/03/01
Sigma-Aldrich
Product number
40324
Product name
2-Nitroaniline solution
Purity
5000?μg/mL in methanol, analytical standard
Packaging
1mL
Price
$51.5
Updated
2022/05/15
TCI Chemical
Product number
N0118
Product name
2-Nitroaniline
Purity
>99.0%(GC)
Packaging
25g
Price
$24
Updated
2023/06/20
TCI Chemical
Product number
N0118
Product name
2-Nitroaniline
Purity
>99.0%(GC)
Packaging
500g
Price
$112
Updated
2023/06/20
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2-Nitroaniline Chemical Properties,Usage,Production

Chemical Properties

orange solid

Uses

2-Nitroaniline is the main precursor to?phenylenediamines, which are converted to?benzimidazoles, a family of?heterocycles?that are key components in pharmaceuticals.

Uses

Dyestuff intermediate.

Production Methods

2-Chloronitrobenzene is heated with excess (10 mol/mol) strong aqueous ammonia in an autoclave. The temperature is gradually increased to 180 ℃ over 4 h and held there for 5 h more. The pressure builds up to around 4 MPa and is released to an ammonia recycle loop before the product is isolated by filtration and washing. The reaction is extremely exothermic, and too rapid heating or inadequate temperature control can result in a runaway reaction. Because of this hazard, I.G. Farbenindustrie developed a continuous amination unit for amination of chloronitrobenzenes; the process is summarized under 4-nitroaniline.

Synthesis Reference(s)

Journal of the American Chemical Society, 77, p. 5688, 1955 DOI: 10.1021/ja01626a066
Organic Syntheses, Coll. Vol. 1, p. 388, 1941

General Description

Orange solid with a musty odor. Sinks and mixes slowly with water.

Air & Water Reactions

Insoluble in water.

Reactivity Profile

2-Nitroaniline may be sensitive to prolonged exposure to light. Mixtures of 2-Nitroaniline with magnesium are hypergolic on contact with nitric acid. 2-Nitroaniline forms extremely explosive addition compounds with hexanitroethane. 2-Nitroaniline has a vigorous reaction with sulfuric acid above 392° F. 2-Nitroaniline is incompatible with acids, acid chlorides, acid anhydrides, chloroformates and strong oxidizers.

Hazard

Explosion risk. Toxic when absorbed by skin.

Health Hazard

Inhalation or ingestion causes headache, nausea, methemo- globinemia, vomiting, weakness, and stupor; cyanosis caused by contact usually develops in 4-6 hrs.; prolonged and excessive exposure may also cause liver damage. Contact with eyes or skin causes irritation; continued exposure may cause same symptoms as inhalation or ingestion.

Fire Hazard

Special Hazards of Combustion Products: Toxic oxides of nitrogen may form in fire.

Safety Profile

A poison. Moderately toxic by ingestion. Mildly toxic by skin contact. Mutation data reported. Mixtures with magnesium are hypergolic on contact with nitric acid. Forms extremely explosive addltion compounds with hexanitroethane. Vigorous reaction with sulfuric acid above 200°C. When heated to decomposition it emits toxic fumes of NOx. See also m- NITROANILINE, p-NITROANILINE, and ANILINE DYES.

Environmental Fate

Biological. Under aerobic and anaerobic conditions using a sewage inoculum, 2-nitroaniline degraded to 2-methylbenzimidazole and 2-nitroacetanilide (Hallas and Alexander, 1983). A Pseudomonas sp. strain P6, isolated from a Matapeake silt loam, did not grow on 2-nitroaniline as the sole source of carbon. However, in the presence of 4-nitroaniline, approximately 50% of the applied 2-nitroaniline metabolized to nonvolatile products which could not be identified by HPLC (Zeyer and Kearney, 1983). In activated sludge inoculum, following a 20-d adaptation period, no degradation was observed (Pitter, 1976).
Plant. 2-Nitroaniline was degraded by tomato cell suspension cultures (Lycopericon lycopersicum). Transformation products identified were 2-nitroanilino-β-D-glucopyranoside, β-(2- amino-3-nitrophenyl)glucopyranoside, and β-(4-amino-3-nitrophenyl)-glucopyranoside (Pogány et al., 1990).

Purification Methods

Crystallise the aniline from hot water (charcoal), then from aqueous 50% EtOH, or EtOH, and dry it in a vacuum desiccator. It has also been chromatographed on alumina, then recrystallised from *benzene. [Beilstein 12 IV 1563.]

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2-Nitroaniline Suppliers

Fuxin Pharmaceutical
Tel
+86-021-021-50872116 +8613122107989
Email
contact@fuxinpharm.com
Country
China
ProdList
10032
Advantage
58
Hubei Zhonglong Kangsheng Fine Chemical Co., Ltd.
Tel
18171205315
Email
1213219329@qq.com
Country
China
ProdList
3623
Advantage
58
Tel
4008-099-669
Email
23419001name@qq.com
Country
CHINA
ProdList
68144
Advantage
58
Tel
010-58103629
Email
185164601name@qq.com
Country
CHINA
ProdList
19437
Advantage
58

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