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8S61336

Supelco

Benzoic acid solution

2000 μg/mL in dichloromethane, analytical standard

Synonyme(s) :

Benzoic acid solution

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About This Item

Formule empirique (notation de Hill):
C7H6O2
Numéro CAS:
65-85-0
Poids moléculaire :
122.12
Numéro CE :
200-838-9
Numéro MDL:
MFCD00002398
Code UNSPSC :
41116107
Nomenclature NACRES :
NA.24

Qualité

analytical standard

Agence

EPA 8270

Pureté

99.90%

Forme

liquid

CofA (certificat d'analyse)

current certificate can be downloaded

Conditionnement

ampule of 2.5 mL

Concentration

2000 μg/mL in dichloromethane

Technique(s)

HPLC: suitable
gas chromatography (GC): suitable

Application(s)

cleaning products
cosmetics
food and beverages
personal care

Format

single component solution

Température de stockage

2-8°C

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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Produits recommandés

This product is being deleted. Product PHR1050-1G may be an acceptable replacement.

Pictogrammes

Health hazardExclamation mark
GHS08,GHS07

Mention d'avertissement

Warning

Mentions de danger

H315,H319,H336,H351

Classification des risques

Carc. 2 - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Organes cibles

Central nervous system

Code de la classe de stockage

6.1D - Non-combustible acute toxic Cat.3 / toxic hazardous materials or hazardous materials causing chronic effects

Classe de danger pour l'eau (WGK)

WGK 2

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable

Équipement de protection individuelle

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

Choose from one of the most recent versions:

Certificats d'analyse (COA)

Lot/Batch Number
LRAD4209
LRAC3228
LC25955V
LC23335V
LC11312

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The transepidermal penetration and metabolic disposition of 14C-benzoyl peroxide were assessed in vitro (excised human skin) and in vivo (rhesus monkey). In vitro, the benzoyl peroxide penetrated into the skin, through the stratum corneum or the follicular openings, or both
Copper-mediated C-H/C-H biaryl coupling of benzoic acid derivatives and 1,3-azoles.
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Angewandte Chemie (International ed. in English), 52(16), 4457-4461 (2013-03-21)
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
Dajie Lin et al.
Biosensors & bioelectronics, 45, 195-200 (2013-03-19)
An amplification strategy for signal tracing was developed by introducing a host-guest binding reaction into the assembly process of gold nanorods (AuNRs) superstructure. The amplification pathway firstly used a thio-β-cyclodextrin (SH-β-CD) functionalized gold nanoparticles to label signal antibody, and then
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