123838

Sigma-Aldrich

Biphenyl-4-methanol

98%

Synonym(s):
4-Phenylbenzyl alcohol, 4-(Hydroxymethyl)biphenyl
Linear Formula:
C6H5C6H4CH2OH
CAS Number:
Molecular Weight:
184.23
Beilstein/REAXYS Number:
1937761
EC Number:
MDL number:
PubChem Substance ID:
NACRES:
NA.22
Pricing and availability is not currently available.

Quality Level

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.

Packaging

10 g in poly bottle

Personal Protective Equipment

dust mask type N95 (US),Eyeshields,Gloves

RIDADR

NONH for all modes of transport

WGK Germany

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Induction of morphological transformation in C3H/10T1/2 clone 8 cells.
A Poole et al.
Mutation research, 100(1-4), 219-221 (1982-01-01)
Copolymerisation of e-caprolactone and trimethylene carbonate catalysed by methanesulfonic acid.
Campos JM, et al.
Eur. Polymer J., 49(12), 4025-4034 (2013)
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)
The Journal of Organic Chemistry, 48, 2603-2603 (1983)
Ryo Mizoguchi et al.
Molecular pharmaceutics, 16(5), 2142-2152 (2019-04-05)
Co-amorphous technology was recently introduced to stabilize drugs in the amorphous state for drug development. We examined the predictability of the formation of co-amorphous systems and identified two reliable indicators of successful formation: (1) a negative Δ Hmix value and...

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