123838
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
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
222-745-2
Beilstein/REAXYS Number:
1937761
MDL number:
Assay:
98%
InChI key
AXCHZLOJGKSWLV-UHFFFAOYSA-N
InChI
1S/C13H12O/c14-10-11-6-8-13(9-7-11)12-4-2-1-3-5-12/h1-9,14H,10H2
SMILES string
OCc1ccc(cc1)-c2ccccc2
assay
98%
mp
96-100 °C (lit.)
solubility
acetone: soluble 25 mg/mL
functional group
hydroxyl, phenyl
Quality Level
Related Categories
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
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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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)
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)
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)
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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