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8S61336

Supelco

SS Benzoic Acid

2000 μg/mL in dichloromethane, analytical standard

Synonym(s):

Benzoic acid solution

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About This Item

Empirical Formula (Hill Notation):
C7H6O2
CAS Number:
65-85-0
Molecular Weight:
122.12
EC Number:
200-838-9
MDL number:
MFCD00002398
UNSPSC Code:
41116107
NACRES:
NA.24

grade

analytical standard

Agency

EPA 8270

Assay

99.90%

form

liquid

CofA

current certificate can be downloaded

packaging

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

storage temp.

2-8°C

InChI

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

InChI key

WPYMKLBDIGXBTP-UHFFFAOYSA-N

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Recommended products

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

Pictograms

Health hazardExclamation mark
GHS08,GHS07

Signal Word

Warning

Hazard Statements

H315,H319,H336,H351

Hazard Classifications

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

Target Organs

Central nervous system

Storage Class Code

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

WGK

WGK 2

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
LRAD4209
LRAC3228
LC25955V
LC23335V
LC11312

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S Nacht et al.
Journal of the American Academy of Dermatology, 4(1), 31-37 (1981-01-01)
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.
Mayuko Nishino et al.
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
Wanchun Xiang et al.
ChemSusChem, 6(2), 256-260 (2013-01-25)
Sensing the sun: Incorporation of a cyanomethyl benzoic acid electron acceptor into donor-π-acceptor sensitizers for dye-sensitized-solar cell is shown to lead to devices with improved conversion efficiency when compared with more widely used cyanoacetic acid acceptor.
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