Identification | More | [Name]
4-Methyl-3-nitrobenzoic acid | [CAS]
96-98-0 | [Synonyms]
2-NITROTOLUENE-4-CARBOXYLIC ACID 3-NITRO-4-METHYLBENZOIC ACID 3-NITRO-P-TOLUIC ACID 4-METHYL-3-NITROBENZOIC ACID AKOS BBS-00007715 RARECHEM AL BO 1292 4-methyl-3-nitro-benzoicaci 4-Methyl-3-Nitrobenzoic Acid 3-Nitro-4-Methylbenzoic Acid 4-Methyl-3-nitrobenzoicacid,99% 4-Methyl-3-nitrobenzoic 3-Nitro-p-toluylsure 4-Methy-3-nitrobenzoic acid 4-METHYL-3-NITROBENZOIC ACID/3-NITRO-P-TOLUIC ACID 3-Nitro-p-toluic acid (COOH=1) | [EINECS(EC#)]
202-549-3 | [Molecular Formula]
C8H7NO4 | [MDL Number]
MFCD00007174 | [Molecular Weight]
181.15 | [MOL File]
96-98-0.mol |
Chemical Properties | Back Directory | [Appearance]
white to light yellow crystal powder | [Melting point ]
187-190 °C (lit.) | [Boiling point ]
314.24°C (rough estimate) | [density ]
1.4283 (rough estimate) | [refractive index ]
1.5468 (estimate) | [storage temp. ]
Sealed in dry,Room Temperature | [solubility ]
0.257g/l | [form ]
Crystalline Powder | [pka]
3.66±0.10(Predicted) | [color ]
White to light yellow | [Water Solubility ]
<0.1 g/100 mL at 22 ºC | [BRN ]
1874411 | [CAS DataBase Reference]
96-98-0(CAS DataBase Reference) | [EPA Substance Registry System]
96-98-0(EPA Substance) |
Safety Data | Back Directory | [Hazard Codes ]
Xn,Xi | [Risk Statements ]
R36/37/38:Irritating to eyes, respiratory system and skin . R20/21/22:Harmful by inhalation, in contact with skin and if swallowed . | [Safety Statements ]
S36/37/39:Wear suitable protective clothing, gloves and eye/face protection . S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice . S22:Do not breathe dust . S36:Wear suitable protective clothing . | [WGK Germany ]
1
| [TSCA ]
Yes | [HS Code ]
29163990 |
Hazard Information | Back Directory | [General Description]
Prismatic crystals or off-white powder. | [Reactivity Profile]
4-METHYL-3-NITROBENZOIC ACID(96-98-0) is a nitrated carboxylic acid. Carboxylic acids donate hydrogen ions if a base is present to accept them. They react in this way with all bases, both organic (for example, the amines) and inorganic. Their reactions with bases, called "neutralizations", are accompanied by the evolution of substantial amounts of heat. Neutralization between an acid and a base produces water plus a salt. Carboxylic acids with six or fewer carbon atoms are freely or moderately soluble in water; those with more than six carbons are slightly soluble in water. Soluble carboxylic acid dissociate to an extent in water to yield hydrogen ions. The pH of solutions of carboxylic acids is therefore less than 7.0. Many insoluble carboxylic acids react rapidly with aqueous solutions containing a chemical base and dissolve as the neutralization generates a soluble salt. Carboxylic acids in aqueous solution and liquid or molten carboxylic acids can react with active metals to form gaseous hydrogen and a metal salt. Such reactions occur in principle for solid carboxylic acids as well, but are slow if the solid acid remains dry. | [Air & Water Reactions]
Insoluble in water. | [Fire Hazard]
Information concerning the flash point of this chemical is not available. 4-METHYL-3-NITROBENZOIC ACID is probably combustible. | [Chemical Properties]
white to light yellow crystal powder | [Uses]
4-Methyl-3-nitrobenzoic acid was used in the synthesis of one-dimensional (1D) lanthanide coordination complexes. | [Purification Methods]
Recrystallise the acid from EtOH. The S-benzylisothiuronium salt has m 167168o (EtOH). The acid chloride [10397-30-5] has m 20-21o, b 185o/36mm, and the methyl ester [7356-11-8] crystallises as pale yellow needles from MeOH with m 51o. [Beilstein 9 H 502, 9 II 334, 9 III 2359.] |
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