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Safety Information

440078

Sigma-Aldrich

Phenyl phenylacetate

96%

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About This Item

Linear Formula:
C6H5CH2CO2C6H5
CAS Number:
722-01-0
Molecular Weight:
212.24
MDL number:
MFCD00216650
UNSPSC Code:
12352100
PubChem Substance ID:
24867563

Assay

96%

form

solid

bp

158 °C/7 mmHg (lit.)

mp

40-42 °C (lit.)

SMILES string

O=C(Cc1ccccc1)Oc2ccccc2

InChI

1S/C14H12O2/c15-14(11-12-7-3-1-4-8-12)16-13-9-5-2-6-10-13/h1-10H,11H2

InChI key

USVNNHYNCCJCCP-UHFFFAOYSA-N

Gene Information

human ... EPHX2(2053)
mouse ... Ephx2(13850)

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

JAN Code

440078-VAR:
440078-25G:
440078-5G:
440078-BULK:

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Certificates of Analysis (COA)

Lot/Batch Number
02612BJ
07930AH
16802CN
08911LS
08022AU

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Molecular rearrangements. Part XX. Thermolysis of carboxylic acid esters.
Aly MM, et al.
Canadian Journal of Chemistry, 61(7), 1532-1535 (1983)
Photochemistry of phenyl phenylacetates adsorbed on pentasil andfaujasite zeolites.
Tung C-H and Ying Y-M.
J. Chem. Soc. Perkin Trans. II, 7, 1319-1322 (1997)
Selectivity in the photo-Fries reaction of phenyl phenylacetates included in a Nafion membrane.
Tung C-H and Xu X-H.
Tetrahedron Letters, 40(1), 127-130 (1999)
C D Carrington et al.
The Biochemical journal, 236(2), 503-507 (1986-06-01)
For the purpose of assessing the neurotoxic potential of organophosphorus compounds, it has been determined that paraoxon-preinhibited hen brain has both neurotoxicant (mipafox)-sensitive (neurotoxic esterase; NTE) and -insensitive esterase components. Several experiments designed to investigate the kinetic parameters governing the
L Haagen et al.
European journal of clinical chemistry and clinical biochemistry : journal of the Forum of European Clinical Chemistry Societies, 30(7), 391-395 (1992-07-01)
A new method for phenotyping human serum arylesterase (EC 3.1.1.2) is described and evaluated. The aromatic esters, phenyl acetate and 4-nitrophenyl acetate, were compared as substrates for spectrophotometric measurement of arylesterase activity. A method for arylesterase phenotyping, based upon inhibition

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