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H25808

Sigma-Aldrich

4-Benzylphenol

99%

Sinónimos:

α-Phenyl-p-cresol, 4-Hydroxydiphenylmethane

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About This Item

Fórmula lineal:
C6H5CH2C6H4OH
Número de CAS:
101-53-1
Peso molecular:
184.23
EC Number:
202-950-3
MDL number:
MFCD00002384
UNSPSC Code:
12352100
PubChem Substance ID:
24895510
NACRES:
NA.22

Quality Level

100

assay

99%

bp

198-200 °C/10 mmHg (lit.)

mp

79-81 °C (lit.)

SMILES string

Oc1ccc(Cc2ccccc2)cc1

InChI

1S/C13H12O/c14-13-8-6-12(7-9-13)10-11-4-2-1-3-5-11/h1-9,14H,10H2

InChI key

HJSPWKGEPDZNLK-UHFFFAOYSA-N

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pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

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

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk_germany

WGK 2

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

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Certificados de análisis (COA)

Lot/Batch Number
MKCS7669
MKCK7616
MKCH8942
MKCC8510
MKBV2968V

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Hanna Andersson et al.
Bioorganic & medicinal chemistry, 16(14), 6924-6935 (2008-06-17)
Analogues of the hexapeptide angiotensin IV (Ang IV, Val(1)-Tyr(2)-Ile(3)-His(4)-Pro(5)-Phe(6)) encompassing a 4-hydroxydiphenylmethane scaffold replacing Tyr(2) and a phenylacetic or benzoic acid moiety replacing His(4)-Pro(5)-Phe(6) have been synthesized and evaluated in biological assays. The analogues inhibited the proteolytic activity of cystinyl
Kei Takemoto et al.
Mutation research, 519(1-2), 199-204 (2002-08-06)
The genotoxic potential of benzophenone and its metabolically related compounds, benzhydrol and p-benzoylphenol, was investigated using human cytochrome P450 (P450) enzymes. Benzophenone and its two metabolites (0.1-1mM) showed a suppression of bacterial growth without any P450 system, but no induction
A W Stocklinski
Xenobiotica; the fate of foreign compounds in biological systems, 11(6), 425-432 (1981-06-01)
1. Urine and faeces, and two-hour bile samples from adult male rats dosed with [14C]diphenylmethane were analysed for benzhydrol and 2- and 4-hydroxydiphenyl-methane by silica gel GF t.l.c. and 14C-determination. 2. Mean values of 48.4% and 17.7% of the administered
Brandi D Sanders et al.
Bioorganic & medicinal chemistry, 17(19), 7031-7041 (2009-09-08)
The sirtuin proteins are broadly conserved NAD(+)-dependent deacetylases that are implicated in diverse biological processes including DNA recombination and repair, transcriptional silencing, longevity, apoptosis, axonal protection, insulin signaling, and fat mobilization. Because of these associations, the identification of small molecule
Peter J McNamara et al.
Antimicrobial agents and chemotherapy, 53(5), 1898-1906 (2009-02-19)
Menstrual toxic shock syndrome is a rare but potentially life-threatening illness manifest through the actions of Staphylococcus aureus toxic shock syndrome toxin 1 (TSST-1). Previous studies have shown that tampon additives can influence staphylococcal TSST-1 production. We report here on
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