| CAS
NO. |
65-85-0 |

|
| EINECS NO. |
200-618-2 |
| FORMULA |
C6H5COOH |
| MOL
WT. |
122.12 |
| H.S.
CODE |
2916.31 |
|
TOXICITY
|
Oral rat LD50:
1700 mg/kg |
| SYNONYMS |
Benzenemethanoic Acid;
Carboxybenzene; |
|
Acide Benzoique
(French); Acido Benzoico; Benzenecarboxylic Acid; Benzeneformic
Acid; Benzoate; Benzoesaeure; Carboxybenzene; Dracylic Acid; Flowers of Benjamin; Flowers Of
Benzoin; Phenylcarboxylic Acid; Phenylformic Acid;
Salvo Liquid; Salvo Powder; Benzoesäure (German); ácido benzoico (Spanish); Acide benzoïque (French); Kyselina Benzoova (Czech); |
|
DERIVATION
|
|
|
CLASSIFICATION
|
CARBOCYCLIC
CARBOXYLIC ACIDS /
|
|
PHYSICAL AND CHEMICAL PROPERTIES
|
| PHYSICAL
STATE |
White,
crystalline flakes
|
| MELTING POINT |
122
C |
| BOILING
POINT |
249
C
|
| SPECIFIC GRAVITY |
1.321 |
| SOLUBILITY
IN WATER |
0.29 g/100 ml |
| pH |
2.8 (saturated solution at
25 C) |
| VAPOR DENSITY |
4.2 |
|
AUTOIGNITION
|
571
C
|
|
REFRACTIVE
INDEX
|
|
|
NFPA
RATINGS
|
Health: 2; Flammability: 1; Reactivity: 0 |
| FLASH
POINT |
121
C
|
| STABILITY |
Stable under ordinary
conditions |
|
GENERAL
DESCRIPTION & APPLICATIONS
|
|
Benzoic acid, the simplest aromatic carboxylic acid containing carboxyl group
bonded directly to benzene ring, is a white, crystalline organic compound;
melting at 122 C (starting sublime at 100 C); boiling at 249 C; slightly
soluble in water, soluble in ethanol, very slightly soluble in benzene and
acetone. Its aqua solution is weakly acidic. It occurs naturally in many plants
and resins. Benzoic acid is also detected in animals. The most of commercial
benzoic acid is produced by the reaction of toluene with oxygen at
temperatures around 200 C in the liquid phase and in the presence of cobalt and
manganese salts as catalysts. It can be prepared also by the oxidation of
benzene with concentrated sulphuric acid or carbon dioxide in the presence of
catalysts. Other methods are such as by the oxidation of benzyl alcohol,
benzaldehyde, cinnamic acid; by hydrolysis of benzonitrile, benzoyl chloride.
More than 90% of commercial benzoic acid is converted directly to phenol and
caprolactam. Its use in the production of glycol benzoates for the application
of plasticizer in adhesive formulations is increasing. It is also used in the
manufacture of alkyd resins and drilling mud additive for crude oil recovery
applications. It is used as a rubber polymerization activators and retardants.
Benzoic acid is converted to its salts and esters for the use of preservative
application in foods, drugs and personal products. Sodium benzoate, sodium salt
of benzoic acid, is used preferably as one of the principal anti-microbial
preservatives used in foods and beverages (but it's concentration is limited
usually not exceeding 0.1% because it is poisonous), as it is about 200 times
more soluble than benzoic acid. Sodium Benzoate is also used in medications,
anti-fermentation additives and tabletting lubricant for pharmaceuticals. The
industrial applications are as a corrosion inhibitor, as an additive to
automotive engine antifreeze coolants and in other waterborne systems, as a
nucleating agents for polyolefin, as a dye intermediate, as a stabilizer in
photographic processing and as a catalyst. Wide range of benzoic esters are used
as solvents, dying carrier, disinfectant additive, penetrating agent and
pesticides and manufacturing other compounds. |
| SALES
SPECIFICATION |
|
APPEARANCE
|
White,
crystalline flakes
|
| ASSAY |
99.5%
min |
| MOISTURE |
0.1%
max
|
| COLOR,
APHA |
50
max
|
|
MELTING
POINT
|
121.5
C min
|
|
RESSIDUE
ON IGNITION
|
0.1%
max
|
| TRANSPORTATION |
| PACKING |
25kgs
bag, 18mts in container
|
| HAZARD CLASS |
|
| UN
NO. |
|
| OTHER
INFORMATION |
|
Hazard
Symbols: XN, Risk Phrases: 22, Safety Phrases: n/a |