Skip to Content
MilliporeSigma
All Photos(1)

Documents

W395900

Sigma-Aldrich

2-Phenylphenol

≥99%, FG

Synonym(s):

o-Phenylphenol, 2-Hydroxybiphenyl

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

About This Item

Linear Formula:
C6H5C6H4OH
CAS Number:
90-43-7
Molecular Weight:
170.21
FEMA Number:
3959
Beilstein/REAXYS Number:
606907
EC Number:
201-993-5
MDL number:
MFCD00002208
UNSPSC Code:
12164502
PubChem Substance ID:
24901953
NACRES:
NA.21

biological source

synthetic

grade

FG

reg. compliance

EU Regulation 1333/2008 & 178/2002
EU Regulation 178/2002
FDA 21 CFR 117

vapor pressure

7 mmHg ( 140 °C)

assay

≥99%

bp

282 °C (lit.)

mp

57-59 °C (lit.)

application(s)

flavors and fragrances

documentation

see Safety & Documentation for available documents

food allergen

no known allergens

organoleptic

odorless

SMILES string

Oc1ccccc1-c2ccccc2

InChI

1S/C12H10O/c13-12-9-5-4-8-11(12)10-6-2-1-3-7-10/h1-9,13H

InChI key

LLEMOWNGBBNAJR-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

General description

2-Phenylphenol is generally used as an anti-fungal agent for the post-harvest protection of citrus fruits.

signalword

Danger

Hazard Classifications

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

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk_germany

WGK 2

flash_point_f

255.2 °F - closed cup

flash_point_c

124 °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’.

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 1

1 of 1

Thiabendazole ≥99%, powder

Sigma-Aldrich

T8904

Thiabendazole

Fungicide residues. Part VI. Determination of residues of post-harvest fungicides on citrus fruit by high-performance liquid chromatography.
Farrow JE, et al.
Analyst, 102(1219), 752-758 (1977)
Han Chen et al.
Bioresource technology, 99(15), 6928-6933 (2008-02-26)
The effect of 2-hydroxybiphenyl (2-HBP), the end product of dibenzothiophene (DBT) desulfurization via 4S pathway, on cell growth and desulfurization activity was investigated by Microbacterium sp. The experimental results indicate that 2-HBP would inhibit the desulfurization activity. Providing 2-HBP was
Ghasemali Mohebali et al.
Microbiology (Reading, England), 153(Pt 5), 1573-1581 (2007-04-28)
It has been previously reported that resting-cells, non-proliferating cells, of Gordonia alkanivorans RIPI90A can convert dibenzothiophene (DBT) to 2-hydroxybiphenyl (2-HBP) via the 4S pathway in a biphasic system. The main goal of the current work was to study the behaviour
Jianqing Li et al.
Toxicology mechanisms and methods, 22(6), 432-437 (2012-03-08)
Ortho-phenylphenol (OPP) has been found to cause carcinomas in the urinary tract of rats. Since OPP is a potent genotoxic compound, and used as fungicides and antibacterial agents in fruits and fruit products, search for newer, better agents for protection
L Alves et al.
Bioresource technology, 102(19), 9162-9166 (2011-07-20)
The acute toxicity of some compounds used in fossil fuels biodesulphurisation studies, on the respiration activity, was evaluated by Gordonia alkanivorans and Rhodococcus erythropolis. Moreover, the effect of 2-hydroxybiphenyl on cell growth of both strains was also determined, using batch
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