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W312908

Sigma-Aldrich

Biphenyl

≥99%

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About This Item

Linear Formula:
C6H5C6H5
CAS Number:
Molecular Weight:
154.21
FEMA Number:
3129
Beilstein:
1634058
EC Number:
Council of Europe no.:
10978
MDL number:
UNSPSC Code:
12164502
PubChem Substance ID:
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

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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

Signal Word

Warning

Hazard Statements

Hazard Classifications

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

Target Organs

Respiratory system

Storage Class Code

13 - Non Combustible Solids

WGK

WGK 2

Flash Point(F)

230.0 °F - closed cup

Flash Point(C)

110 °C - closed cup

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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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
Shi-Rong Liu et al.
Organic letters, 15(4), 878-881 (2013-02-05)
A BODIPY-based fluorescent probe, HCSe, has been successfully developed for the rapid detection of hypochlorous acid based on the specific HOCl-promoted oxidation of diphenyl selenide in response to the amount of HOCl. Confocal fluorescence microscopy imaging using RAW264.7 cells showed
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
Ondrej Uhlik et al.
PloS one, 7(7), e40653-e40653 (2012-07-19)
Bacteria were identified associated with biodegradation of aromatic pollutants biphenyl, benzoate, and naphthalene in a long-term polychlorinated biphenyl- and polyaromatic hydrocarbon-contaminated soil. In order to avoid biases of culture-based approaches, stable isotope probing was applied in combination with sequence analysis
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

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