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W312908

Sigma-Aldrich

Biphenyl

≥99%

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About This Item

Linear Formula:
C6H5C6H5
CAS Number:
92-52-4
Molecular Weight:
154.21
FEMA Number:
3129
Beilstein/REAXYS Number:
1634058
EC Number:
202-163-5
Council of Europe no.:
10978
MDL number:
MFCD00003054
UNSPSC Code:
12164502
PubChem Substance ID:
24901476
Flavis number:
1.013
NACRES:
NA.21

biological source

synthetic

agency

meets purity specifications of JECFA

vapor density

5.31 (vs air)

vapor pressure

9.46 mmHg ( 115 °C)

assay

≥99%

form

flakes
powder or crystals

autoignition temp.

1004 °F

expl. lim.

0.6 %, 111 °F
5.8 %, 166 °F

bp

255 °C (lit.)

mp

68-70 °C (lit.)

application(s)

flavors and fragrances

documentation

see Safety & Documentation for available documents

food allergen

no known allergens

organoleptic

geranium; green

SMILES string

c1ccc(cc1)-c2ccccc2

InChI

1S/C12H10/c1-3-7-11(8-4-1)12-9-5-2-6-10-12/h1-10H

InChI key

ZUOUZKKEUPVFJK-UHFFFAOYSA-N

Gene Information

human ... CYP1A2(1544) , ESR1(2099)

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General description

Biphenyl is an aromatic hydroacarbon that is generally used as a preservative for citrus fruits.

Disclaimer

For R&D or non-EU Food use. Not for retail sale.

pictograms

Exclamation markEnvironment
GHS07,GHS09

signalword

Warning

Hazard Classifications

Aquatic Acute 1 - Aquatic Chronic 1 - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

13 - Non Combustible Solids

wgk_germany

WGK 2

flash_point_f

230.0 °F - closed cup

flash_point_c

110 °C - closed cup

ppe

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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Drazenka Selesi et al.
FEMS microbiology ecology, 68(1), 86-93 (2009-02-04)
The aromatic hydrocarbon biphenyl is a widely distributed environmental pollutant. Whereas the aerobic degradation of biphenyl has been extensively studied, knowledge of the anaerobic biphenyl-oxidizing bacteria and their biochemical degradation pathway is scarce. Here, we report on an enrichment culture
Xiaofeng Chen et al.
The Journal of organic chemistry, 77(17), 7572-7578 (2012-08-07)
A highly efficient cross-coupling of diarylborinic acids and anhydrides with aryl chlorides and bromides has been effected by using a palladium catalyst system co-supported by a strong σ-donor N-heterocyclic carbene (NHC), N,N'-bis(2,6-diisopropylphenyl) imidazol-2-ylidene, and a strong π-acceptor phosphite, triphenylphosphite, in
Sheng-Hao Hsu et al.
Acta biomaterialia, 8(11), 4151-4161 (2012-07-31)
Low-shrinkage resin-based photocurable liquid crystalline epoxy nanocomposite has been investigated with regard to its application as a dental restoration material. The nanocomposite consists of an organic matrix and an inorganic reinforcing filler. The organic matrix is made of liquid crystalline
Guoxiang Jiang et al.
Carbohydrate polymers, 92(1), 758-764 (2012-12-12)
Ultrasound-assisted extraction was employed to extract polysaccharides from longan seed (LSP), with aids of a Box-Behnken statistical design to investigate the effects of ultrasonic power, time and liquid/solid ratio on the extraction recovery of the LSP. The structural analysis indicated
Frédéric R Leroux et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 18(45), 14232-14236 (2012-09-29)
A modular way towards biaryls: Highly enantioenriched biphenyls can be prepared based on a transition-metal-free aryl-aryl coupling followed by efficient desymmetrization or deracemization and chemoselective functionalization (see scheme).
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