Skip to Content
MilliporeSigma
All Photos(1)

Key Documents

View All Documentation

13761

Sigma-Aldrich

2-Benzylphenol

≥98.0% (GC)

Synonym(s):

α-Phenyl-o-cresol, 2-Hydroxydiphenylmethane

Sign Into View Organizational & Contract Pricing
All Photos(1)

About This Item

Linear Formula:
C6H5CH2C6H4OH
CAS Number:
28994-41-4
Molecular Weight:
184.23
Beilstein/REAXYS Number:
2045725
EC Number:
249-361-8
MDL number:
MFCD00002242
UNSPSC Code:
12352100
PubChem Substance ID:
57647115
NACRES:
NA.22

Quality Level

100

assay

≥98.0% (GC)

form

solid

bp

312 °C (lit.)

mp

49-51 °C (lit.)
49-51 °C

solubility

methanol: soluble 1 g/10 mL, clear, almost colorless

functional group

phenyl

SMILES string

Oc1ccccc1Cc2ccccc2

InChI

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

InChI key

CDMGNVWZXRKJNS-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

Application

2-Benzylphenol was used as starting reagent in the synthesis of 2-benzylacetate. It was also used in the the synthesis of 6- and 8-benzyl derivatives of 2-(dialkylamino)chromones.

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 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
BCCF7919
338593/1
338593/1
330838/1
324127/1

Don't see the Right Version?

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

Search for a COA

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Masateru Ono et al.
Chemical & pharmaceutical bulletin, 50(10), 1416-1417 (2002-10-10)
A new ortho-benzoyloxyphenyl acetic acid ester, called vaccihein A (1), was isolated from the fruit of rabbiteye blueberry (Vaccinium ashei). The chemical structure was determined on the basis of spectroscopic data. Compound 1 had antioxidative activity using the ferric thiocyanate
A Balbi et al.
Il Farmaco; edizione scientifica, 37(9), 582-596 (1982-09-01)
Some 2-(dialkylamino)chromones phenyl substituted in position 6 or 7 or 8 were synthesized by reaction of N,N-dialkylethoxycarbonylacetamides with 4- or 3- or 2-biphenylol, respectively, in the presence of phosphorus oxychloride. The pharmacological activity of these compounds was then evaluated and
Yu-Zhe Chen et al.
Photochemical & photobiological sciences : Official journal of the European Photochemistry Association and the European Society for Photobiology, 8(7), 916-925 (2009-07-08)
Photo-Fries rearrangements and associated photoreactions of four o-cresyl acylates were investigated in cyclohexane and in unstretched and stretched polyethylene (PE) films with different degrees of crystallinity. The esters differ in the number of phenyl substituents attached to the methyl group
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

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service