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About This Item
Linear Formula:
H2NC6H3(C6H5)OH
CAS Number:
Molecular Weight:
185.22
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Recommended Products
grade
technical grade
Assay
90%
form
powder
mp
198-202 °C (lit.)
functional group
phenyl
SMILES string
Nc1cc(ccc1O)-c2ccccc2
InChI
1S/C12H11NO/c13-11-8-10(6-7-12(11)14)9-4-2-1-3-5-9/h1-8,14H,13H2
InChI key
IGIDZGNPFWGICD-UHFFFAOYSA-N
General description
2-Amino-4-phenylphenol is an aminoalcohol derivative. It participates in the synthesis of bisbenzoxazoles.
Application
2-Amino-4-phenylphenol is suitable as an internal standard to investigate the enzymatic activity of N-hydroxy-N-2-fluorenylacetamide (N-OH-2-FAA), a mammary gland carcinogen in the female Sprague-Dawley rat, by HPLC.
It may be used as a chelating agent for metal ions.
It may be used as a chelating agent for metal ions.
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 4 Dermal - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Target Organs
Respiratory system
Storage Class Code
11 - Combustible Solids
WGK
WGK 2
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
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Metal ion complexing properties of carcinogen metabolites.
J H WEISBURGER et al.
Biochemical pharmacology, 12, 179-191 (1963-02-01)
Synthesis and properties of 4, 4'-bis [5-alkyl (aryl) benzoxazol-2-yl]-2-hydroxy (alkoxy) biphenyls.
Ol'khovik VK, et al.
Russ. J. Org. Chem., 42(8), 1164-1168 (2006)
C L Ritter et al.
Carcinogenesis, 17(11), 2411-2418 (1996-11-01)
N-Hydroxy-N-2-fluorenylacetamide (N-OH-2-FAA) and its benzamide analogue N-OH-2-FBA are mammary gland carcinogens in the female Sprague-Dawley rat. Ovariectomy inhibits tumorigenicity of topically applied N-OH-2-FAA suggesting modulation of carcinogen-activating enzymes in the gland. This study concerned the activation of N-OH-2-FAA and N-OH-2-FBA
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