| Identification | More | [Name]
1-Methoxy-2,4-dinitrobenzene | [CAS]
119-27-7 | [Synonyms]
2,4-DINITROANISOLE
2,4-DINITROMETHOXYBENZENE
1-methoxy-2,4-dinitro-benzen
1-Methoxy-2,4-dinitrobenzene
1-methoxy-2,4-dinitro-Benzene
2,4-Dinitro-1-methoxy-benzene
2,4-Dinitroanisol
2,4-dinitro-anisol
2,4-Dinitrophenyl methyl ether
2,4-dinitrophenylmethylether
2,4-Nitroanisole
alpha-Dinitroanisole
Anisole, 2,4-dinitro-
Dinitroanisole
-Dinitroanisole
2,4-Dinitroanisole99%
2,4-dimitroanisole
3,4-Dinitromethoxybenzene
1,3-Dinitro-4-methoxybenzene | [EINECS(EC#)]
204-310-9 | [Molecular Formula]
C7H6N2O5 | [MDL Number]
MFCD00035745 | [Molecular Weight]
198.13 | [MOL File]
119-27-7.mol |
| Safety Data | Back Directory | [Hazard Codes ]
Xn | [Risk Statements ]
R20/21/22:Harmful by inhalation, in contact with skin and if swallowed .
R40:Limited evidence of a carcinogenic effect.
R22:Harmful if swallowed. | [Safety Statements ]
S7/8:Keep container tightly closed and dry .
S22:Do not breathe dust .
S36/37/39:Wear suitable protective clothing, gloves and eye/face protection . | [WGK Germany ]
3
| [RTECS ]
DA5250000
| [TSCA ]
Yes | [HazardClass ]
6.1 | [Safety Profile]
Poison by ingestion.
Mutation data reported. When heated to
decomposition it emits toxic fumes of NOx.
See also NITRO COMPOUNDS of
AROMATIC HYDROCARBONS and
NITRATES. | [Toxicity]
rat,LDLo,oral,100mg/kg (100mg/kg),National Academy of Sciences, National Research Council, Chemical-Biological Coordination Center, Review. Vol. 5, Pg. 16, 1953. |
| Hazard Information | Back Directory | [Chemical Properties]
yellow crystals or crystalline powder | [Uses]
It can be used as a dye ingredient. It is one of the insensitive nitroaromatic ingredients increasingly used as a replacement for 2,4,6-trinitrotoluene (TNT) in munitions. | [Definition]
ChEBI: A member of the class of dinitroanisoles that is 2-nitroanisole in which the hydrogen para to the methoxy group is replaced by a second nitro group. | [Production Methods]
2,4-Dinitrochlorobenzene is treated with methanolic sodium hydroxide in a process similar to that described for 4-nitroanisole. 2,4-Dinitrophenetole [610-54-8] is similarly manufactured by using ethanol. | [Flammability and Explosibility]
Notclassified | [Purification Methods]
Purify the anisole by repeated crystallisation from EtOH, MeOH or H2O and dry it in a vacuum desiccator over P2O5. The naphthalene complex has m 69o (from EtOH). [Beilstein 6 III 869, 6 IV 1385. |
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