Skip to Content
MilliporeSigma
All Photos(1)

Documents

123838

Sigma-Aldrich

Biphenyl-4-methanol

98%

Synonym(s):

4-(Hydroxymethyl)biphenyl, 4-Phenylbenzyl alcohol

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

About This Item

Linear Formula:
C6H5C6H4CH2OH
CAS Number:
3597-91-9
Molecular Weight:
184.23
Beilstein/REAXYS Number:
1937761
EC Number:
222-745-2
MDL number:
MFCD00004660
UNSPSC Code:
12352100
PubChem Substance ID:
24847585
NACRES:
NA.22

Quality Level

100

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

Looking for similar products? Visit Product Comparison Guide

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_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

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’.

Already Own This Product?

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

Visit the Document Library

Customers Also Viewed

Slide 1 of 5

1 of 5

Biphenyl-4-carboxylic acid 95%

Sigma-Aldrich

B34729

Biphenyl-4-carboxylic acid

Biphenyl-4-thiol 97%

Sigma-Aldrich

752207

Biphenyl-4-thiol

1-Indanone ReagentPlus®, ≥99%

Sigma-Aldrich

I2304

1-Indanone

4-Bromobenzyl alcohol 99%

Sigma-Aldrich

187054

4-Bromobenzyl alcohol

4-Methylbenzyl alcohol 98%

Sigma-Aldrich

127809

4-Methylbenzyl alcohol

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)
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
Mutation at the TK locus of mouse lymphoma L5178Y cells by 4CMB, 4HMB and BC.
C A Ross et al.
Mutation research, 100(1-4), 249-251 (1982-01-01)
Transformation of BHK 21 C13 cells by BC, 4CMB and 4HMB using the method of Styles.
A Poole et al.
Mutation research, 100(1-4), 215-217 (1982-01-01)
View All Related Papers

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