Hordenine

Modify Date: 2024-01-01 22:49:35

Hordenine Structure
Hordenine structure
Common Name Hordenine
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
GHS07
Signal Word Warning

 Use of Hordenine


Hordenine, an alkaloid found in plants, inhibits melanogenesis by suppression of cyclic adenosine monophosphate (cAMP) production[1].

 Names

Name hordenine
Synonym More Synonyms

 Hordenine Biological Activity

Description Hordenine, an alkaloid found in plants, inhibits melanogenesis by suppression of cyclic adenosine monophosphate (cAMP) production[1].
Related Catalog
References

[1]. Kim SC, et al. Hordenine, a single compound produced during barley germination, inhibits melanogenesis in human melanocytes. Food Chem. 2013 Nov 1;141(1):174-81.

 Chemical & Physical Properties

Density 1.0±0.1 g/cm3
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

 Safety Information

Symbol GHS07
GHS07
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

 Synthetic Route

 Customs

HS Code 2922199090
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%

 Articles24

More Articles
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...

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...

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...

 Synonyms

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
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