3-Methyl-4-nitrobenzoic acid

$ 1.00 /1kg

Min. Order1 kg
Purity99%
Cas No3113-71-1
Supply AbilityCARA14
Update time2019-07-06

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Chemical Properties

Product Name	3-Methyl-4-nitrobenzoic acid
CAS No	3113-71-1
EC-No	221-479-4
Min. Order	1 kg
Purity	99%
Supply Ability	CARA14
Release date	2019/07/06

3-Methyl-4-nitrobenzoic acid Basic information

Product Name:	3-Methyl-4-nitrobenzoic acid
Synonyms:	3-METHYL-4-NITROBENZOIC ACID FOR SYNTHES;Methyl-4-nitrobenzoic;5-Carboxy-2-nitrotoluene, 4-Nitro-m-toluic acid;RARECHEM AL BO 0346;3-methyl-4-nitro-benzoicaci;Benzoic acid, 3-methyl-4-nitro-;m-Toluic acid, 4-nitro-;4-NITRO-3-METHYLBENZOIC ACID
CAS:	3113-71-1
MF:	C8H7NO4
MW:	181.15
EINECS:	221-479-4
Product Categories:	Aromatic Carboxylic Acids, Amides, Anilides, Anhydrides & Salts;Benzoic acid;Organic acids;pharmaceutical intermediates
Mol File:	3113-71-1.mol

3-Methyl-4-nitrobenzoic acid Chemical Properties

Melting point	216-218 °C(lit.)
Boiling point	314.24°C (rough estimate)
density	1.4283 (rough estimate)
refractive index	1.5468 (estimate)
storage temp.	Store below +30°C.
form	Amorphous Powder
color	Yellow
Water Solubility	<0.1 g/100 mL at 22 ºC
BRN	1959154
CAS DataBase Reference	3113-71-1(CAS DataBase Reference)
NIST Chemistry Reference	3-Methyl-4-nitrobenzoic acid(3113-71-1)
EPA Substance Registry System	Benzoic acid, 3-methyl-4-nitro-(3113-71-1)

Safety Information

Hazard Codes	Xi,Xn
Risk Statements	36/37/38-20/21/22
Safety Statements	26-36-36/37/39-22
WGK Germany	3
Hazard Note	Irritant
TSCA	Yes
HS Code	29163900

MSDS Information

Provider	Language
3-Methyl-4-nitrobenzoic acid	English
ACROS	English
SigmaAldrich	English
ALFA	English

3-Methyl-4-nitrobenzoic acid Usage And Synthesis

Chemical Properties	white to light yellow crystal powder
General Description	Needles or off white powder.
Air & Water Reactions	Insoluble in water.
Reactivity Profile	3-Methyl-4-nitrobenzoic acid 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.
Fire Hazard	Flash point data for 3-Methyl-4-nitrobenzoic acid are not available; however, 3-Methyl-4-nitrobenzoic acid is probably combustible.

3-Methyl-4-nitrobenzoic acid Preparation Products And Raw materials

Preparation Products

ethyl 4-chloroquinazoline-6-carboxylate-->4-Methyl-2-n-propyl-1H-benzimidazole-6-carboxylic acid-->7-METHYL-2-PROPYL-1H-BENZOIMIDAZOLE-5-CARBOXYLIC ACID METHYL ESTER-->3,4-dihydro-4-oxoquinazoline-6-carboxylic acid-->4-aminobenzene-1,3-dioic acid-->Methyl 4-amino-3-methylbenzoate-->4-NITROISOPHTHALIC ACID

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3-Methyl-4-nitrobenzoic acid

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