| Weight | 33.998 g/mol |
|---|---|
| Formula | H3P |
| Hydrogen Acceptors | 0 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 0 |
Phosphine
phosphane · hydrogen phosphorus, PH3
7803-51-2, 51457-48-8, 12185-10-3, 7723-14-0
Score:
#26 in Physics
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- Palladium-Catalyzed Suzuki-Miyaura Cross-coupling Reactions Employing Dialkylbiaryl Phosphine Ligands (Accounts of Chemical Research, 2008)
- Mixed phosphine 2,2-bipyridine complexes of ruthenium (Inorganic Chemistry, 1978)
- Biaryl Phosphane Ligands in Palladium-Catalyzed Amination (Angewandte Chemie, 2008)
- Cyclometalated Phosphine-Based Pincer Complexes: Mechanistic Insight in Catalysis, Coordination, and Bond Activation (Chemical Reviews, 2003)
- Vibrational Spectra and Bonding in Metal Carbonyls. I. Infrared Spectra of Phosphine-substituted Group VI Carbonyls in the CO Stretching Region (Journal of the American Chemical Society, 1962)
- Selective carbon-carbon bond formation by cross-coupling of Grignard reagents with organic halides. Catalysis by nickel-phosphine complexes (Journal of the American Chemical Society, 1972)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - H220: Extremely flammable gas
Danger Flammable gases - Category 1 - H228: Flammable solid
Warning Flammable solids - Category 2 - H250: Catches fire spontaneously if exposed to air
Danger Pyrophoric liquids; Pyrophoric solids - Category 1 - H314: Causes severe skin burns and eye damage
Danger Skin corrosion/irritation - Category 1A, B, C - H330: Fatal if inhaled
Danger Acute toxicity, inhalation - Category 1, 2 - H400: Very toxic to aquatic life
Warning Hazardous to the aquatic environment, acute hazard - Category 1 - phosphane
- hydrogen phosphorus, PH3
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SMILESP
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- Pubchem - Phosphine
- Wikipedia - phosphine
Phosphine (IUPAC name: phosphane) is the compound with the chemical formula PH3. It is a colorless, flammable, toxic gas and pnictogen hydride. Pure phosphine is odorless, but technical grade samples have a highly unpleasant odor like garlic or rotting fish, due to the presence of substituted phosphine and diphosphane (P2H4).
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