2-Nitroanisole Chemical Properties

Melting point:

9-12 °C (lit.)

Boiling point:

273 °C (lit.)

Density 

1.254 g/mL at 25 °C (lit.)

refractive index 

n20/D 1.561(lit.)

Flash point:

>230 °F

storage temp. 

Refrigerator, Under Inert Atmosphere

solubility 

alcohol: soluble(lit.)

form 

Oil

color 

Pale Yellow

Specific Gravity

1.254

Water Solubility 

1.45 g/L (20 ºC)

Merck 

14,6584

BRN 

1868032

Dielectric constant

43.0

Stability:

Stable. Incompatible with strong oxidizing agents.

CAS DataBase Reference

91-23-6(CAS DataBase Reference)

IARC

2A (Vol. 65, 127)

NIST Chemistry Reference

Benzene, 1-methoxy-2-nitro-(91-23-6)

EPA Substance Registry System

o-Nitroanisole (91-23-6)

Safety Information

Hazard Codes 

T

Risk Statements 

45-22

Safety Statements 

53-45

RIDADR 

UN 2730 6.1/PG 3

WGK Germany 

3

RTECS 

BZ8790000

TSCA 

Yes

HazardClass 

6.1

PackingGroup 

III

HS Code 

29093090

Hazardous Substances Data

91-23-6(Hazardous Substances Data)

MSDS

• Language:English Provider:2-Nitroanisole
• Language:English Provider:SigmaAldrich
• Language:English Provider:ACROS
• Language:English Provider:ALFA

2-Nitroanisole Usage And Synthesis

Chemical Properties

yellow to amber liquid

Chemical Properties

2-Nitroanisole is a yellowish or light-red to amber liquid. May be transported in molten form.

Uses

2-Nitroanisole has been employed as solvatochromic probe to examine cybotactic region of pure and mixed supercritical fluid solvent systems.

Uses

2-Nitroanisole is an intermediate in the synthesis of various potential therapeutic compounds.

Production Methods

Methanolic sodium hydroxide is added slowly to a solution of 2- chloronitrobenzene in methanol at 70 ℃; the mixture is then heated gradually to 95 ℃ under pressure to complete the reaction. After dilution with water the product 2-Nitroanisole is separated as an oil, in 90 % yield, and methanol is recovered from the aqueous layer.

Definition

ChEBI: A member of the class of 2-nitroanisoles that is anisole in which one of the hydrogens ortho to the methoxy group is replaced by a nitro group.

Synthesis Reference(s)

Tetrahedron Letters, 29, p. 4501, 1988 DOI: 10.1016/S0040-4039(00)80531-6

General Description

2-Nitroanisole (2-methoxynitrobenzene is an industrial and environmental pollutant causing tumors of the urinary bladder in rats and mice. Tumorigenic potential of 2-nitroanisole has been evaluated by host-mediated in vitro and in vivo assay.

Hazard

Questionable carcinogen.

Safety Profile

Confirmed carcinogen. Moderately toxic by ingestion. Mutation data reported. Explosive reaction with sodium hydroxide + zinc. Vigorous reaction with hydrogen + catalyst (at 250°C/34bar). When heated to decomposition it emits toxic fumes of NOx. See also p- NITROANISOLE.

Potential Exposure

A dye intermediate and for synthesis of other chemicals. NFPA has reported an explosion on during reduction with a nickel catalyst. Occupational exposure to 2-nitroanisole may occur through inhalation and dermal contact with this compound at workplaces where the chemical is produced or used.

Carcinogenicity

o-Nitroanisole is reasonably anticipated to be a human carcinogenbased on sufficient evidence of carcinogenicity from studies in experimental animals.

Shipping

UN2730 Nitroanisoles, liquid, Hazard Class: 6.1; Labels: 6.1-Poisonous materials. UN3458 Nitroanisoles, solid, Hazard Class: 6.1; Labels: 6.1-Poisonous materials.

Purification Methods

Purify it by repeated vacuum distillation in the absence of oxygen. [Beilstein 6 IV 1249.]

Incompatibilities

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. Explodes at temperatures ＞110℃. Combustible-liquid or fine powder may form explosive mixture with air. Nitroanisole reacts explosively with (sodium hydroxide ＋ zinc). It reacts vigorously with hydrogen1 catalyst (@ 250℃ & 25,500 mmHg).

Waste Disposal

Use a licensed professional waste disposal service to dispose of this material. Dissolve or mix the material with a combustible solvent and burn in a chemical incinerator equipped with an afterburner and scrubber. All federal, state, and local environmental regulations must be observed.

2-Nitroanisole(91-23-6)Related Product Information

• 3-Nitrobenzaldehyde
• 3-Nitroanisole
• 4-Nitrobenzoic acid
• 2-Methoxyethanol
• Sodium 3-nitrobenzenesulphonate
• Nitrobenzene
• 4-Methyl-2-nitroanisole
• 1,3-Dinitrobenzene
• 1-Methoxy-2,4-dinitrobenzene
• 3-Methyl-2-nitroanisole
• 4-Methoxy-3-nitrobenzoic acid
• 2,5-Dimethoxy-4-nitroaniline
• 5-METHOXY-2-METHYL-4-NITROANILINE, TECH., 95
• 3-METHOXY-2-NITROBENZOIC ACID
• 3-Methoxy-4-nitrobenzoic acid
• 3-METHOXY-4-NITROBENZYL ALCOHOL
• 4-Nitroanisole
• 2-Nitroanisole