3-Aminophenol
3-Aminophenol structure
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Common Name | 3-Aminophenol | ||
|---|---|---|---|---|
| CAS Number | 591-27-5 | Molecular Weight | 109.126 | |
| Density | 1.2±0.1 g/cm3 | Boiling Point | 164 ºC (11 mmHg) | |
| Molecular Formula | C6H7NO | Melting Point | 121-124 ºC | |
| MSDS | Chinese USA | Flash Point | 155 ºC | |
| Symbol |
GHS07, GHS09 |
Signal Word | Warning | |
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Cellular apoptosis and cytotoxicity of phenolic compounds: a quantitative structure-activity relationship study.
J. Med. Chem. 48 , 7234-42, (2005) In this comprehensive study on the caspase-mediated apoptosis-inducing effect of 51 substituted phenols in a murine leukemia cell line (L1210), we determined the concentrations needed to induce caspase activity by 50% (I50) and utilized these data to develop ... |
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Recombinant Human Semenogelin-1 (Sg1) and Sg1 (1-159) form Detergent Stable Amyloid like Aggregates in vitro.
Protein Pept. Lett. 23 , 87-96, (2015) Senile seminal vesicle amyloidosis (SSVA) is associated with deposition of semenogelin-1 (Sg1) protein aggregates in seminal vesicles that may manifest as hematospermia. Sg1 is the predominant protein that entraps spermatozoa which are freed upon fragmentatio... |
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Influence of age on the absorption, metabolism, and excretion of cocoa flavanols in healthy subjects.
Mol. Nutr. Food. Res. 59 , 1504-12, (2015) An understanding of the pharmacokinetics of structurally related (-)-epicatechin metabolites (SREM) is a prerequisite for considering cocoa flavanols (CF) in the context of dietary recommendations. The objective of this study was to compare the absorption, me... |
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Spectrophotometric determination of folic acid in pharmaceutical preparations by coupling reactions with iminodibenzyl or 3-aminophenol or sodium molybdate-pyrocatechol.
Anal. Biochem. 307(2) , 316-21, (2002) Novel coupling reagents are used for the simple and sensitive spectrophotometric determination of folic acid either in pure form or in its pharmaceutical preparations. The methods are based on the probable diazotization of the p-aminobenzoylglutamic acid obta... |
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[Determination of seven aromatic amines in hair dyes by capillary electrophoresis coupled with field-amplified sample stacking].
Se Pu 29(11) , 1122-7, (2011) A method for the determination of 4,4'-methylenedianiline, aniline, o-anisidine, 3, 4-dimethylaniline, p-anisidine, 3-aminophenol, 1-naphthylamine in hair dyes was established by capillary electrophoresis coupled with field-amplified sample stacking. The opti... |
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Simultaneous spectrophotometric determination of PAS and its degradation product m-aminophenol.
Pharm. Acta Helv. 63(11) , 290-3, (1988)
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Catalytic antibodies: the rerouting of chemical reactions. Towards electrophilic aromatic substitution by carbon dioxide.
Ann. N. Y. Acad. Sci. 799 , 26-31, (1996)
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Toxic effects of aminophenols on aquatic life using the zebrafish embryo test and the comet assay.
Bull. Environ. Contam. Toxicol. 73(4) , 628-34, (2004)
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Isolation and characterization of a Pseudomonas sp. strain PH1 utilizing meta-aminophenol.
Can. J. Microbiol. 46(3) , 211-7, (2000) Pseudomonas sp. strain PH1 was isolated from soil contaminated with pharmaceutical and dye industry waste. The isolate PH1 could use m-aminophenol as a sole source of carbon, nitrogen, and energy to support the growth. PH1 could degrade up to 0.32 mM m-aminop... |
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Examination and expansion of the substrate range of m-hydroxybenzoate hydroxylase.
Biochem. Biophys. Res. Commun. 371(1) , 149-53, (2008) The gene encoding m-hydroxybenzoate hydroxylase (mobA) was cloned from Comamonas testosteroni GZ39. MobA converts m-hydroxybenzoate and to a lesser extent p-hydroxybenzoate to protocatechuate. To explore the structural and functional relationships in phenolic... |