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Merck

242381

Sigma-Aldrich

Benzoesäure

ACS reagent, ≥99.5%

Synonym(e):

Benzenecarboxylic acid, Carboxybenzene

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About This Item

Lineare Formel:
C6H5COOH
CAS-Nummer:
Molekulargewicht:
122.12
Beilstein:
636131
EG-Nummer:
MDL-Nummer:
UNSPSC-Code:
12352100
eCl@ss:
39023903
PubChem Substanz-ID:
NACRES:
NA.21

Qualität

ACS reagent

Qualitätsniveau

Dampfdichte

4.21 (vs air)

Dampfdruck

10 mmHg ( 132 °C)

Assay

≥99.5%

Form

crystalline

Selbstzündungstemp.

1061 °F

Verpackung

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

Verunreinigungen

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

Glührückstand

≤0.005%

bp

249 °C (lit.)

mp (Schmelzpunkt)

121-125 °C (lit.)

Löslichkeit

water: soluble (2.9 g/l at 25 °C)

Anionenspuren

chloride (Cl-): ≤0.005%

Kationenspuren

heavy metals (as Pb): ≤5 ppm

Funktionelle Gruppe

carboxylic acid
phenyl

SMILES String

OC(=O)c1ccccc1

InChI

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

InChIKey

WPYMKLBDIGXBTP-UHFFFAOYSA-N

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Allgemeine Beschreibung

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.

Anwendung

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.

Piktogramme

Health hazardCorrosion

Signalwort

Danger

Gefahreneinstufungen

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

Zielorgane

Lungs

Lagerklassenschlüssel

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

WGK

WGK 1

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable


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Die Dokumentenbibliothek aufrufen

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
Ly Dieu Tran et al.
Journal of the American Chemical Society, 134(44), 18237-18240 (2012-10-30)
An auxiliary-assisted, copper catalyzed or promoted sulfenylation of benzoic acid derivative β-C-H bonds and benzylamine derivative γ-C-H bonds has been developed. The method employs disulfide reagents, copper(II) acetate, and DMSO solvent at 90-130 °C. Application of this methodology to the

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