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Merck

242381

Sigma-Aldrich

Benzoic acid

ACS reagent, ≥99.5%

Sinónimos:

Benzenecarboxylic acid, Carboxybenzene

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About This Item

Fórmula lineal:
C6H5COOH
Número de CAS:
Peso molecular:
122.12
Beilstein:
636131
Número CE:
Número MDL:
Código UNSPSC:
12352100
eCl@ss:
39023903
ID de la sustancia en PubChem:
NACRES:
NA.21

grado

ACS reagent

Nivel de calidad

densidad de vapor

4.21 (vs air)

presión de vapor

10 mmHg ( 132 °C)

Análisis

≥99.5%

formulario

crystalline

temp. de autoignición

1061 °F

envase

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

impurezas

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

residuo de ign.

≤0.005%

bp

249 °C (lit.)

mp

121-125 °C (lit.)

solubilidad

water: soluble (2.9 g/l at 25 °C)

trazas de anión

chloride (Cl-): ≤0.005%

trazas de catión

heavy metals (as Pb): ≤5 ppm

cadena SMILES

OC(=O)c1ccccc1

InChI

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

Clave InChI

WPYMKLBDIGXBTP-UHFFFAOYSA-N

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Descripción general

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.

Aplicación

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.

Pictogramas

Health hazardCorrosion

Palabra de señalización

Danger

Frases de peligro

Clasificaciones de peligro

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

Órganos de actuación

Lungs

Código de clase de almacenamiento

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

Clase de riesgo para el agua (WGK)

WGK 1

Punto de inflamabilidad (°F)

Not applicable

Punto de inflamabilidad (°C)

Not applicable


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Visite la Librería de documentos

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

Artículos

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.

Protocolos

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

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