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Merck
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Documentos

8S61336

Supelco

Benzoic acid solution

2000 μg/mL in dichloromethane, analytical standard

Sinónimos:

Benzoic acid solution

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About This Item

Fórmula empírica (notación de Hill):
C7H6O2
Número de CAS:
65-85-0
Peso molecular:
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

signalword

Warning

Hazard Classifications

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

target_organs

Central nervous system

Storage Class

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

wgk_germany

WGK 2

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

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

Choose from one of the most recent versions:

Certificados de análisis (COA)

Lot/Batch Number
LRAD4209
LRAC3228
LC25955V
LC23335V
LC11312

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If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

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Benzoic acid ≥99.5%, FCC, FG

Sigma-Aldrich

W213101

Benzoic acid

Benzoic acid analytical standard, (for the calibration of the melting point system), traceable to primary standards (LGC)

Supelco

73983

Benzoic acid

Naphthalene analytical standard

Supelco

84679

Naphthalene

Acetato de etilo anhydrous, 99.8%

Sigma-Aldrich

270989

Acetato de etilo

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
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
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)
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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