Skip to Content
Merck
CN

W395900

2-Phenylphenol

≥99%, FG

Synonym(s):

o-Phenylphenol, 2-Hydroxybiphenyl

Sign In to View Organizational & Contract Pricing.

Select a Size

About This Item

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

Key Documents

View All Documentation
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist

InChI key

LLEMOWNGBBNAJR-UHFFFAOYSA-N

InChI

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

SMILES string

Oc1ccccc1-c2ccccc2

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

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

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

Regulatory Information

危险化学品
This item has

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
SHBM3352
SHBM2272
STBJ0028
MKBW9166V
MKBV2818V

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Search for a COA

Already Own This Product?

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

Visit the Document Library

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)
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
Shujuan Zhang et al.
Water research, 44(6), 2067-2074 (2010-01-15)
With the significant increase in the production and use of carbon nanotubes (CNTs), they will be inevitably released into aquatic environments. Therefore, the fate and transport of CNTs in aqueous solutions have attracted extensive attention. In the present work, the
D Murray et al.
Environmental technology, 31(4), 455-466 (2010-05-11)
Algal blooms are a significant problem in the UK, particularly in water sources that supply potable water treatment works. A wide range of methods to control algae have been tested and, whilst many are effective, they all have disadvantages. The
Shusuke Tani et al.
Mutation research, 628(2), 123-128 (2007-01-26)
Oxidative mutation is mainly induced by reactive oxygen species (ROS), such as the superoxide anion radical (O(2)(-)) and hydrogen peroxide (H(2)O(2)). However, in Escherichia coli (E. coli), ROS are eliminated by enzymes such as superoxide dismutase and catalase, which are
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