Hordenine structure
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Common Name | Hordenine | ||
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CAS Number | 539-15-1 | Molecular Weight | 165.232 | |
Density | 1.0±0.1 g/cm3 | Boiling Point | 270.2±23.0 °C at 760 mmHg | |
Molecular Formula | C10H15NO | Melting Point | N/A | |
MSDS | Chinese USA | Flash Point | 123.5±21.3 °C | |
Symbol |
GHS07 |
Signal Word | Warning |
Use of HordenineHordenine, an alkaloid found in plants, inhibits melanogenesis by suppression of cyclic adenosine monophosphate (cAMP) production[1]. |
Name | hordenine |
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Synonym | More Synonyms |
Description | Hordenine, an alkaloid found in plants, inhibits melanogenesis by suppression of cyclic adenosine monophosphate (cAMP) production[1]. |
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Related Catalog | |
References |
Density | 1.0±0.1 g/cm3 |
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Boiling Point | 270.2±23.0 °C at 760 mmHg |
Molecular Formula | C10H15NO |
Molecular Weight | 165.232 |
Flash Point | 123.5±21.3 °C |
Exact Mass | 165.115356 |
PSA | 23.47000 |
LogP | 1.40 |
Vapour Pressure | 0.0±0.6 mmHg at 25°C |
Index of Refraction | 1.542 |
Symbol |
GHS07 |
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Signal Word | Warning |
Hazard Statements | H302-H317-H319 |
Precautionary Statements | P280-P305 + P351 + P338 |
Hazard Codes | Xn |
Risk Phrases | 22-36-43 |
Safety Phrases | 26-36/37 |
RIDADR | NONH for all modes of transport |
HS Code | 2922199090 |
Precursor 10 | |
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DownStream 10 | |
HS Code | 2922199090 |
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Summary | 2922199090. other amino-alcohols, other than those containing more than one kind of oxygen function, their ethers and esters; salts thereof. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0% |
Development of immunoassays for tyramine and tryptamine toxins of Phalaris aquatica L.
J. Agric. Food Chem. 48(1) , 27-32, (2000) The leaves of the perennial pasture grass Phalaris aquatica L. (phalaris) contain two groups of known toxins, indole alkaloids, primarily dimethyltryptamines and N-methyltyramines, which cause illness... |
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Some hematological and histopathological effects of the alkaloids gramine and hordenine on meadow voles (Microtus pennsylvanicus).
Toxicology 18(2) , 125-31, (1980) Meadow voles (Microtus pennsylvanicus) were used to evaluate the relative toxicity of the alkaloids, gramine and hordenine, which are present in reed canarygrass (Phalaris arundinacea) and to assess t... |
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Rapid formation of N-nitrosodimethylamine from gramine, a naturally occurring precursor in barley malt.
IARC Sci. Publ. (57) , 337-46, (1984) The two tertiary amine alkaloids, hordenine and gramine, which are biosynthesized in malt during germination, were subjected to nitrosation under conditions typical for the study of tertiary amine nit... |
4-[2-(Dimethylamino)ethyl]phenol |
Cactine |
Anhaline |
Peyocactine |
N,N-dimethyltyramine |
Hordenin |
Phenol, 4-[2-(dimethylamino)ethyl]- |
Hordetin |
Hordenine |
p-[2-(Dimethylamino)ethyl]phenol |
2-(4-Hydroxyphenyl)-N,N-dimethylethylamine (4-(2-Dimethylaminoethyl)phenol |
MFCD00051462 |
p-Hydroxy-N,N-dimethylphenethylamine |
4-(2-(Dimethylamino)ethyl)phenol |
Ordenina |
Eremursine |
EINECS 222-740-5 |
Anhalin |
Phenol, p-[2-(dimethylamino)ethyl]- |
Ordenine |
4-Hydroxy-N,N-dimethylphenethylamine |
N,N-Dimethyl-p-hydroxyphenethylamine |
Anhalin-d6 |
N,N-dimethyl-2-(4-hydroxyphenyl)ethylamine |