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123838

Sigma-Aldrich

Biphenyl-4-methanol

98%

Synonym(s):

4-(Hydroxymethyl)biphenyl, 4-Phenylbenzyl alcohol

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About This Item

Linear Formula:
C6H5C6H4CH2OH
CAS Number:
Molecular Weight:
184.23
Beilstein:
1937761
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Assay

98%

mp

96-100 °C (lit.)

solubility

acetone: soluble 25 mg/mL

SMILES string

OCc1ccc(cc1)-c2ccccc2

InChI

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

InChI key

AXCHZLOJGKSWLV-UHFFFAOYSA-N

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General description

Biphenyl-4-methanol acts as monofunctional alcohol initiator during the ring-opening polymerization of trimethylene carbonate (TMC) catalyzed by CH3SO3H and copolymerisation of ε-caprolactone and TMC.

Application

Biphenyl-4-methanol was used as reagent for the rapid quantitative determination of lithium alkyls.

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

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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A New Insight Into the Mechanism of the Ring-Opening Polymerization of Trimethylene Carbonate Catalyzed by Methanesulfonic Acid.
Campos JM, et al.
Macromolecular Chemistry and Physics, 214(1), 85-93 (2013)
The Journal of Organic Chemistry, 48, 2603-2603 (1983)
UKEMS trial compounds: induction of unscheduled DNA synthesis in HeLa S3 cells.
R H Barrett
Mutation research, 100(1-4), 207-209 (1982-01-01)
DNA damage and its repair in cultured human alveolar tumor cells treated with benzyl chloride, 4-chloromethylbiphenyl or 4-hydroxymethylbiphenyl.
R Mirzayans et al.
Mutation research, 100(1-4), 203-206 (1982-01-01)
The cytotoxic and mutagenic effects of 4CMB, BC and 4HMB in V79 Chinese hamster cells.
F Mirzayans et al.
Mutation research, 100(1-4), 239-244 (1982-01-01)

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