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5-Methyl-2-nitrobenzoic acid

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5-Methyl-2-nitrobenzoic acid Basic information

Product Name:
5-Methyl-2-nitrobenzoic acid
Synonyms:
  • 5-METHYL-2-NITROBENZOIC ACID
  • 6-NITRO-M-TOLUIC ACID
  • 6-NITRO-M-TOLUYLIC ACID
  • 3-METHYL-6-NITROBENZOIC ACID
  • 5-methyl-2-nitro-benzoicaci
  • 2-NITRO-5-METHYLBENZOIC ACID
  • 6-nitro-p-toluic acid
  • 5-Methyl-2-nitrobenzoic
CAS:
3113-72-2
MF:
C8H7NO4
MW:
181.15
EINECS:
221-481-5
Product Categories:
  • Aromatic Carboxylic Acids, Amides, Anilides, Anhydrides & Salts
  • Benzoic acid
Mol File:
3113-72-2.mol
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5-Methyl-2-nitrobenzoic acid Chemical Properties

Melting point:
134-136 °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
form 
Powder or Crystalline Powder
pka
2.21±0.25(Predicted)
color 
White to yellow
Water Solubility 
4.7g/L(20 ºC)
BRN 
1959031
Stability:
Stable. Incompatible with strong oxidizing agents.
CAS DataBase Reference
3113-72-2(CAS DataBase Reference)
EPA Substance Registry System
5-Methyl-2-nitrobenzoic acid (3113-72-2)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-36/37/39-37
WGK Germany 
3
TSCA 
Yes
HS Code 
29163990

MSDS

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5-Methyl-2-nitrobenzoic acid Usage And Synthesis

Chemical Properties

off-white crystalline powder

Uses

5-Methyl-2-nitrobenzoic acid is used in the preparation of methyl-N-(5-methyl-2-nitrophenyl) carbamate.

General Description

Crystals or very light yellow solid.

Air & Water Reactions

Insoluble in water.

Reactivity Profile

5-Methyl-2-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 5-Methyl-2-nitrobenzoic acid are not available; however, 5-Methyl-2-nitrobenzoic acid is probably combustible.

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