N-Phenylhydroxylamine structure
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Common Name | N-Phenylhydroxylamine | ||
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CAS Number | 100-65-2 | Molecular Weight | 109.12600 | |
Density | 1.214g/cm3 | Boiling Point | 215.8ºC at 760mmHg | |
Molecular Formula | C6H7NO | Melting Point | 83 - 84ºC | |
MSDS | Chinese USA | Flash Point | 120.2ºC | |
Symbol |
GHS06 |
Signal Word | Danger |
Name | N-phenylhydroxylamine |
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Synonym | More Synonyms |
Density | 1.214g/cm3 |
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Boiling Point | 215.8ºC at 760mmHg |
Melting Point | 83 - 84ºC |
Molecular Formula | C6H7NO |
Molecular Weight | 109.12600 |
Flash Point | 120.2ºC |
Exact Mass | 109.05300 |
PSA | 32.26000 |
LogP | 1.56070 |
Vapour Pressure | 0.085mmHg at 25°C |
Index of Refraction | 1.649 |
Storage condition | ?20°C |
Stability | Unstable - deteriorates with storage. Incompatible with strong oxidizing agents. |
CHEMICAL IDENTIFICATION
HEALTH HAZARD DATAACUTE TOXICITY DATA
MUTATION DATA
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Precursor 8 | |
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DownStream 10 | |
HS Code | 2928000090 |
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Summary | 2928000090 other organic derivatives of hydrazine or of hydroxylamine VAT:17.0% Tax rebate rate:9.0% Supervision conditions:none MFN tariff:6.5% General tariff:20.0% |
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Genotoxic activities of aniline and its metabolites and their relationship to the carcinogenicity of aniline in the spleen of rats.
Crit. Rev. Toxicol. 35(10) , 783-835, (2005) Aniline (in the form of its hydrochloride) has been shown to induce a rather rare spectrum of tumors in the spleen of Fischer 344 rats. The dose levels necessary for this carcinogenic activity were in... |
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Biotransformation of hydroxylaminobenzene and aminophenol by Pseudomonas putida 2NP8 cells grown in the presence of 3-nitrophenol.
Appl. Environ. Microbiol. 66(6) , 2336-42, (2000) Biotransformation products of hydroxylaminobenzene and aminophenol produced by 3-nitrophenol-grown cells of Pseudomonas putida 2NP8, a strain grown on 2- and 3-nitrophenol, were characterized. Ammonia... |
N-Phenylhydroxylamine |
EINECS 202-875-6 |