P28808
Phenylphosphinic acid
99%
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About This Item
Linear Formula:
C6H5P(O)(OH)H
CAS Number:
Molecular Weight:
142.09
Beilstein:
2802244
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Quality Level
Assay
99%
form
powder
mp
83-85 °C (lit.)
SMILES string
O[PH](=O)c1ccccc1
InChI
1S/C6H7O2P/c7-9(8)6-4-2-1-3-5-6/h1-5,9H,(H,7,8)
InChI key
MLCHBQKMVKNBOV-UHFFFAOYSA-N
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General description
Phenylphosphinic acid is also known as phenylphosphonous acid. Kinetics of oxidation of phenylphosphinic acid by metal and non metal oxidants was investigated in a study.2
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 4 Oral - Skin Corr. 1B
Storage Class Code
8A - Combustible corrosive hazardous materials
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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E Maria Donner et al.
Drug and chemical toxicology, 26(2), 125-133 (2003-06-21)
Phenylphosphinic acid was fed in graded concentrations of either 0 (control), 100, 1,000, or 10,000 ppm to rats for 28 days. These concentrations provided average daily doses of 8, 76, and 779 mg/kg (males) and 9, 83, and 859 mg/kg
Loïc J Charbonnière et al.
Inorganic chemistry, 44(20), 7151-7160 (2005-09-27)
A new ligand, LC, bis-[(6'-carboxy-2,2'-bipyridine-6-yl)]phenylphosphine oxide, in which the tridentate 6-carboxy-2,2'-bipyridyl arms are directly linked to a phenylphosphine oxide fragment, has been synthesized. The corresponding [Ln.LC]Cl.xH2O complexes (Ln = Eu, x = 4, and Tb, x = 3) were isolated
Kunio Ikemura et al.
Dental materials journal, 28(3), 267-276 (2009-08-11)
The behavior of water-soluble photoinitiators with crown ethers in dental adhesives is unknown. This study investigated the effect of sodium acylphosphine oxide (APO-Na) with crown ether in a hydrophobic adhesive on adhesion to teeth. Sodium 2,4,6-trimethylbenzoyl-phenylphosphine oxide (TMPO-Na = APO-Na)
Li-Biao Han et al.
The Journal of organic chemistry, 70(24), 10121-10123 (2005-11-19)
[reaction: see text] A variety of functionalized optically pure (R(P))-alkylphenylphosphinates are readily prepared by stereospecific radical or base-catalyzed additions of the easily available (R(P))-menthyl phenylphosphinate to alkenes.
J Seliger et al.
Magnetic resonance in chemistry : MRC, 46(10), 969-973 (2008-08-23)
The (17)O nuclear quadrupole resonance (NQR) frequencies have been measured in phenylphosphinic acid and phenylphosphonic acid using nuclear quadrupole double resonance. The quadrupole coupling constants have been determined with an uncertainty of +/- 10 kHz and the asymmetry parameter eta
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