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04476

Sigma-Aldrich

Hordenine

≥97.0% (HPLC)

Synonym(s):

2-(4-Hydroxyphenyl)-N,N-dimethylethylamine, 4-(2-Dimethylaminoethyl)phenol, N,N-Dimethyltyramine, p-Hydroxy-N,N-dimethylphenethylamine, Anhaline, Cactine, Eremursin, Peyocactine

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50 MG
MYR 660.00

MYR 660.00


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50 MG
MYR 660.00

About This Item

Empirical Formula (Hill Notation):
C10H15NO
CAS Number:
Molecular Weight:
165.23
Beilstein:
2207615
EC Number:
MDL number:
UNSPSC Code:
41116107
PubChem Substance ID:
NACRES:
NA.25

MYR 660.00


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Quality Level

Assay

≥97.0% (HPLC)

form

powder or crystals

application(s)

metabolomics
vitamins, nutraceuticals, and natural products

SMILES string

CN(C)CCc1ccc(O)cc1
CN(C)CCc1ccc(O)cc1

InChI

1S/C10H15NO/c1-11(2)8-7-9-3-5-10(12)6-4-9/h3-6,12H,7-8H2,1-2H3

InChI key

KUBCEEMXQZUPDQ-UHFFFAOYSA-N

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This Item
GF59285863GF10944457GF23070990
Nickel rod, diam. 6.35 mm, ≥99.99% trace metals basis

267074

Nickel

assay

≥99.99% trace metals basis

assay

99%

assay

99%

assay

99%

form

rod

form

rod

form

rod

form

rod

density

8.9 g/mL at 25 °C (lit.)

density

8.9 g/mL at 25 °C (lit.)

density

8.9 g/mL at 25 °C (lit.)

density

8.9 g/mL at 25 °C (lit.)

bp

2732 °C (lit.)

bp

2732 °C (lit.)

bp

2732 °C (lit.)

bp

2732 °C (lit.)

mp

1453 °C (lit.)

mp

1453 °C (lit.)

mp

1453 °C (lit.)

mp

1453 °C (lit.)

resistivity

6.97 μΩ-cm, 20°C

resistivity

6.97 μΩ-cm, 20°C

resistivity

6.97 μΩ-cm, 20°C

resistivity

6.97 μΩ-cm, 20°C

Application

Hordenine is suitable to study the effect of reed canary grass alkoloids on in vito digestibility. It is also suitable for use as a standard to identify endogenous hordenine in ungerminated and germinated barley by HPLC/diode array detection analysis.[1] Hordenine may be used as an analytical reference material and in research on the activities of phenethylamine type alkaloids.

Biochem/physiol Actions

Hordenine is an alkaloid found in plants, e.g. the roots of germinating barley[2][3] and marine algae.[4] It is a metabolite in tyrosine metabolism, biosynthesized from tyramine by two subsequent N-methylations,[5] it is metabolized by monoamine oxidase.[6] Hordenine is a sympathomimetic and its pharmacological actions are of interest, as it is occasionally found in post race urine samples.[7] Hordenine inhibits melanogenesis by suppression of cyclic adenosine monophosphate (cAMP) production. cAMP is involved in the expression of melanogenesis-related proteins. Hordenine may be used in the inhibition of hyperpigmentation.[1] It is present in barley roots from the first day of seed germination, but is not present in seeds.[8]

Packaging

Bottomless glass bottle. Contents are inside inserted fused cone.

Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable


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