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242381

Sigma-Aldrich

Acide benzoique

ACS reagent, ≥99.5%

Synonyme(s) :

Benzenecarboxylic acid, Carboxybenzene

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About This Item

Formule linéaire :
C6H5COOH
Numéro CAS:
Poids moléculaire :
122.12
Numéro Beilstein :
636131
Numéro CE :
Numéro MDL:
Code UNSPSC :
12352100
eCl@ss :
39023903
ID de substance PubChem :

Qualité

ACS reagent

Niveau de qualité

Densité de vapeur

4.21 (vs air)

Pression de vapeur

10 mmHg ( 132 °C)

Pureté

≥99.5%

Forme

crystalline

Température d'inflammation spontanée

1061 °F

Conditionnement

poly bottle of 25, 100, 500 g
poly drum of 3 kg

Impuretés

MnO4- reducers, passes test
≤0.002% S compounds
≤0.005% CH3OH insol.

Résidus de calcination

≤0.005%

Point d'ébullition

249 °C (lit.)

Pf

121-125 °C (lit.)

Solubilité

water: soluble (2.9 g/l at 25 °C)

Traces d'anions

chloride (Cl-): ≤0.005%

Traces de cations

heavy metals (as Pb): ≤5 ppm

Chaîne SMILES 

OC(=O)c1ccccc1

InChI

1S/C7H6O2/c8-7(9)6-4-2-1-3-5-6/h1-5H,(H,8,9)

Clé InChI

WPYMKLBDIGXBTP-UHFFFAOYSA-N

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Catégories apparentées

Description générale

Benzoic acid is an organic aromatic monocarboxylic acid. It can be synthesized by the cobalt or manganese catalyzed atmospheric oxidation of toluene. Recently, benzoic acid has been prepared from toluene by employing TiO2 nanotubes electrode.
Benzoic acid reacts with hydrogenating reagents to afford hexahydrobenzoic acid. The thermal decomposition of the product in the presence of lime or alkali produces benzene and carbon dioxide.

Application

Benzoic acid has been used in the preparation of vials for the HPLC analysis of various polyamines in biological fluids, tissues and isolated/cultured cells.
It may be employed as an intermediate in the synthesis of the following:
  • paints
  • pigments
  • varnish
  • wetting agents
  • aroma compounds
  • benzoyl chloride
  • benzotrichloride
It may also be used to investigate the mechanism of complex addition reaction of hydroxyl radicals with various aromatic compounds.

Pictogrammes

CorrosionHealth hazard

Mention d'avertissement

Danger

Mentions de danger

Classification des risques

Eye Dam. 1 - Skin Irrit. 2 - STOT RE 1 Inhalation

Organes cibles

Lungs

Code de la classe de stockage

6.1C - Combustible, acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

Classe de danger pour l'eau (WGK)

WGK 1

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable


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Les clients ont également consulté

Zhaolai Dai et al.
Amino acids, 46(6), 1557-1564 (2014-03-19)
Polyamines (putrescine, spermine and spermidine) play a crucial role in the regulation of cell growth, differentiation, death and function. Accurate measurement of these substances is essential for studying their metabolism in cells. This protocol describes detailed procedures for sample preparation
Hydroxylation by electrochemically generated OH. radicals. Mono-and polyhydroxylation of benzoic acid: products and isomer distribution.
Oturan MA and Pinson J.
The Journal of Physical Chemistry, 99(38), 13948-13954 (1995)
Eagleson M.
Concise Encyclopedia Chemistry, 122-122 (1994)
Shutang Tan et al.
Cell reports, 33(9), 108463-108463 (2020-12-03)
The widely used non-steroidal anti-inflammatory drugs (NSAIDs) are derivatives of the phytohormone salicylic acid (SA). SA is well known to regulate plant immunity and development, whereas there have been few reports focusing on the effects of NSAIDs in plants. Our
G C Tremblay et al.
Pharmacology & therapeutics, 60(1), 63-90 (1993-10-01)
Detoxification of sodium benzoate by elimination as a conjugate with glycine, a nonessential amino acid, provides a pathway for the disposal of waste nitrogen. Since 1979, sodium benzoate has been widely used in the therapeutic regimen to combat ammonia toxicity

Articles

Acid and base chart lists the strength of acids and bases (strongest to weakest) in order. Simple to use laboratory reference chart for scientists, researchers and lab technicians.

Protocoles

Separation of 4-Hydroxybenzoic acid; Acetylsalicylic acid; Benzoic acid; Salicylic acid; Ethyl 4-hydroxybenzoate

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