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8S61336

Supelco

SS Benzoesäure

2000 μg/mL in dichloromethane, analytical standard

Synonym(e):

Benzoesäure -Lösung

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About This Item

Empirische Formel (Hill-System):
C7H6O2
CAS-Nummer:
65-85-0
Molekulargewicht:
122.12
EG-Nummer:
200-838-9
MDL-Nummer:
MFCD00002398
UNSPSC-Code:
41116107
NACRES:
NA.24

Qualität

analytical standard

Agentur

EPA 8270

Assay

99.90%

Form

liquid

Analysenzertifikat (CofA)

current certificate can be downloaded

Verpackung

ampule of 2.5 mL

Konzentration

2000 μg/mL in dichloromethane

Methode(n)

HPLC: suitable
gas chromatography (GC): suitable

Anwendung(en)

cleaning products
cosmetics
food and beverages
personal care

Format

single component solution

Lagertemp.

2-8°C

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

Piktogramme

Health hazardExclamation mark
GHS08,GHS07

Signalwort

Warning

Gefahreneinstufungen

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

Zielorgane

Central nervous system

Lagerklassenschlüssel

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

WGK

WGK 2

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable

Persönliche Schutzausrüstung

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

Choose from one of the most recent versions:

Analysenzertifikate (COA)

Lot/Batch Number
LRAD4209
LRAC3228
LC25955V
LC23335V
LC11312

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Benzoesäure ≥99.5%, FCC, FG

Sigma-Aldrich

W213101

Benzoesäure

Mettler-Toledo Kalibriersubstanz ME 18555, Benzoesäure analytical standard, (for the calibration of the melting point system), traceable to primary standards (LGC)

Supelco

73983

Mettler-Toledo Kalibriersubstanz ME 18555, Benzoesäure

Naphthalin analytical standard

Supelco

84679

Naphthalin

Ethylacetat anhydrous, 99.8%

Sigma-Aldrich

270989

Ethylacetat

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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.
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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
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