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4-Nitroaniline

CAS No.
100-01-6
Chemical Name:
4-Nitroaniline
Synonyms
PNA;P-NITROANILINE;PARA NITRO ANILINE;4-NITROBENZENAMINE;P-nitroanilide;4-Nitro-phenylamine;P-NITROPHENYLAMINE;red2gbase;developerp;devolredgg
CBNumber:
CB9852549
Molecular Formula:
C6H6N2O2
Molecular Weight:
138.12
MDL Number:
MFCD00007858
MOL File:
100-01-6.mol
MSDS File:
SDS
Last updated:2024-02-18 17:28:16

4-Nitroaniline Properties

Melting point 147 °C
Boiling point 332 °C
Density 1,437 g/cm3
vapor density 4.77 (vs air)
vapor pressure 1.33 hPa (142 °C)
refractive index 1.6465 (estimate)
Flash point 329 °F
storage temp. Store below +30°C.
solubility ethanol: soluble25mg/mL, slightly hazy, yellow to brownish-yellow
pka 1(at 25℃)
Colour Index 37035
form crystalline
color yellow
Specific Gravity 1.437
Odor Ammonia odor
PH Range 7
Water Solubility 0.8 g/L (20 ºC)
Merck 14,6584
BRN 508690
Henry's Law Constant 1.15 x 10-9 atm?m3/mol at 25 °C (thermodynamic method-GC/UV spectrophotometry, Altschuh et al., 1999)
Exposure limits NIOSH REL: TWA 3; IDLH 300; OSHA PEL: TWA 6; ACGIH TLV: TWA 3 (adopted).
Dielectric constant 56.3(160.0℃)
Stability Stable. Incompatible with sodium hydroxide, strong oxidizing agents, strong reducing agents. May attack some plastics, rubber and coatings. May decompose explosively in the presence of initiators. Moisture sensitive. May be light and air-sensitive.
LogP 1.2 at 30℃
CAS DataBase Reference 100-01-6(CAS DataBase Reference)
EWG's Food Scores 2
FDA UNII 1MRQ0QZG7G
NIST Chemistry Reference p-Nitroaniline(100-01-6)
EPA Substance Registry System p-Nitroaniline (100-01-6)

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictogramsGHS hazard pictograms
GHS06,GHS08
Signal word  Danger
Hazard statements  H301+H311+H331-H373-H412
Precautionary statements  P273-P280-P301+P310-P302+P352+P312-P304+P340+P311-P314
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-16-1/2-7
RIDADR  UN 1661 6.1/PG 2
WGK Germany  2
RTECS  BY7000000
8
Autoignition Temperature 500 °C
Hazard Note  Toxic
TSCA  Yes
HazardClass  6.1
PackingGroup  II
HS Code  29214210
Toxicity Acute LD50 for wild birds 75 mg/kg, guinea pigs 450 mg/kg, mice 810 mg/kg, quail 1,000 mg/kg, rats 750 mg/kg (quoted, RTECS, 1985).
IDLA 300 mg/m3
NFPA 704
1
3 2

4-Nitroaniline Chemical Properties,Uses,Production

Chemical Properties

p-Nitroaniline consists of yellow crystals with a pungent, faint ammonia-like odor.

Chemical Properties

Yellow fine crystals

Physical properties

Bright yellow crystalline powder or flakes with a faint, ammonia-like, slightly pungent odor. Combustible.

Uses

Product of chromogenic reactions.

Uses

Dyestuff intermediate.

Uses

4-Nitroaniline is used in the synthesis of photorefractive polymers, as novel chromophores in analytical study. As well, due to the absorption spectrum associated with 4-Nitroaniline, it is used to de termine catechol derivatives in syntheses.

Definition

ChEBI: A nitroaniline carrying a nitro group at position 4.

Synthesis Reference(s)

The Journal of Organic Chemistry, 59, p. 4114, 1994 DOI: 10.1021/jo00094a021
Synthetic Communications, 20, p. 293, 1990 DOI: 10.1080/00397919008052297

General Description

Yellow solid with a mild odor. Sinks in water.

Air & Water Reactions

4-Nitroaniline may be sensitive to prolonged exposure to air and light. Insoluble in water. 4-Nitroaniline is sensitive to moisture.

Reactivity Profile

P-NITROANILINE may react vigorously with sulfuric acid above 392° F. 4-Nitroaniline may also react with sodium hydroxide at 266° F. Under pressure, 4-Nitroaniline may produce an explosive compound. 4-Nitroaniline is incompatible with strong oxidizers and strong reducing agents. 4-Nitroaniline is capable of explosive decomposition with strong initiators. 4-Nitroaniline will attack some forms of plastics, rubber and coatings.

Hazard

Explosion risk. Toxic when absorbed by skin. Methemoglobinemia, liver damage and eye irritant. Questionable carcinogen.

Health Hazard

Inhalation or ingestion causes headache, drowsiness, shortness of breath, nausea, methemoglobinemia, and unconsciousness; fingernails, lips, and ears become bluish; prolonged and excessive exposures may also cause liver damage. Contact with eyes causes irritation and possible corneal damage. Contact with skin causes irritation; continued exposure may cause same symptoms as inhalation or ingestion.

Flammability and Explosibility

Non flammable

Safety Profile

Poison by ingestion, intravenous, and intraperitoneal routes. Moderately toxic by intramuscular route. Mutation data reported. Acute symptoms of exposure are headache, nausea, vomiting, weakness and stupor, cyanosis and methemoglobinemia. Chronic exposure can cause liver damage. Experimental reproductive effects. Combustible when exposed to heat or flame. See NITRATES for explosion and disaster hazards. To fight fire, use water spray or mist, foam, dry chemical, CO2. Vigorous reaction with sulfuric acid above 200°C. Reaction with sodium hydroxide at 13O°C under pressure may produce the explosive sodium-4-nitrophenoxide. When heated to decomposition it emits toxic fumes of NOx. See also m- NITROANILINE, o-NITROANILINE, NITRO COMPOUNDS OF AROMATIC HYDROCARBONS, and ANILINE DYES.

Potential Exposure

p-Nitroaniline is used as an intermediate in the manufacture of dyes; antioxidants, pharmaceuticals, antiozonants, colors, pigments and pesticides.

Carcinogenicity

p-Nitroaniline has been tested in several strains of S. typhimurium. It was mutagenic in strain TA98 but not in strains TA97, TA100, TA1535, and TA1537, with and without S9. It caused gene mutation in mouse lymphoma cells and chromosomal aberrations in CHO cells in the presence of S9.

Environmental Fate

Biological. A Pseudomonas sp. strain P6, isolated from a Matapeake silt loam, was grown using a yeast extract. After 8 d, 4-nitroaniline degraded completely to carbon dioxide (Zeyer and Kearney, 1983). In activated sludge inoculum, following a 20-d adaptation period, no degradation was observed (Pitter, 1976).
Chemical/Physical: Spacek et al. (1995) investigated the photodegradation of 4-nitroaniline using titanium dioxide-UV light and Fenton’s reagent (hydrogen peroxide:substance – 10:1; Fe2+ 2.5 x 10-4 mol/L). Both experiments were conducted at 25 °C. The decomposition rate of 4-nitroaniline was very high by the photo-Fenton reaction in comparison to titanium dioxide-UV light (λ = 365 nm). Decomposition products identified in both reactions were nitrobenzene, pbenzoquinone, hydroquinone, oxalic acid, and resorcinol. Oxalic acid, hydroquinone, and pbenzoquinone were identified as intermediate products using HPLC.
At influent concentrations of 10, 1.0, 0.1, and 0.01 mg/L, the GAC adsorption capacities were 250, 140, 74, and 40 mg/g, respectively (Dobbs and Cohen, 1980).

Shipping

UN1661 Nitroanilines (m-, o-, p-), Hazard Class: 6.1; Labels: 6.1-Poisonous materials.

Purification Methods

It also crystallises from acetone. It is freed from o-and m-isomers by zone melting and sublimation. [Beilstein 12 IV 1613.]

Incompatibilities

A combustible liquid. A strong oxidizer. Incompatible with strong acids; sulfur, combustibles, organics, and other easily oxidizable materials. Will accelerate the burning of combustible materials. If large quantities are involved in a fire or the combustible material is finely divided, an explosion may result. Prolonged exposure to fire or heat may result in an explosion.

Waste Disposal

Incineration (982℃, 2.0 seconds minimum) with scrubbing for nitrogen oxides abatement. Consult with environmental regulatory agencies for guidance on acceptable disposal practices. Generators of waste containing this contaminant (≥100 kg/mo) must conform with EPA regulations governing storage, transportation, treatment, and waste disposal.

4-NITROANILINE STD SOLUTION 0.1 MOL/L N18, 1 L 4-NitroanilineA.R. 4-NitroanilinePure-(P-NitroAniline) 4-Nitroaniline,>97% 4-NitroanilineGr 4-NitroanilinePure P-NitroAniline(Pna)99% p-NITROANILINE extrapure p-NITROANILINE extrapure AR +Kitronnilin 4-Aminonitrobenzene 4-Nitraniline 4-nitro-anilin 4-nitro-benzenamin Aniline, 4-nitro- Aniline, p-nitro- aniline,p-nitro Azoamine Red 2H Azoamine Red Zh azoamineredzh Azofix Red GG Salt azofixredggsalt Azoic Diazo Component 37 azoicdiazocomponent37 Benzenamine, 4-nitro- Benzenamine,4-nitro- C.I. Azoic Diazo Component 37 C.I. Developer 17 c.i.azoicdiazocomponent37 c.i.developer17 ciazoicdiazocomponent37 cideveloper17 Developer P developerp Devol Red GG devolredgg Diazo Fast Red GG diazofastredgg Fast Red 2G Base Fast Red 2G Salt Fast Red Base 2J Fast Red Base GG Fast Red GG Base Fast Red MP Base Fast Red P Base Fast Red P Salt Fast Red Salt 2J Fast Red Salt GG fastred2gbase fastred2gsalt fastredbase2j fastredbasegg fastredggbase fastredmpbase fastredpbase fastredpsalt fastredsalt2j fastredsaltgg