Basic information Safety Supplier Related

DL-M-O-METHYLEPINEPHRINE HYDROCHLORIDE

Basic information Safety Supplier Related

DL-M-O-METHYLEPINEPHRINE HYDROCHLORIDE Basic information

Product Name:
DL-M-O-METHYLEPINEPHRINE HYDROCHLORIDE
Synonyms:
  • (+-)-4-hydroxy-3-methoxy-alpha-((methylamino)methyl)benzenemethanolhydrochlo
  • 3-methoxy-adrenalinhydrochloride
  • 4-hydroxy-3-methoxy-alpha-((methylamino)methyl)-benzenemethanohydrochlorid
  • alpha-((methylamino)methyl)-vanillylalcohohydrochloride
  • 4-HYDROXY-3-METHOXY-ALPHA-[METHYLAMINOMETHYL]BENZENE-METHANOL HYDROCHLORIDE
  • 4-HYDROXY-3-METHOXY-ALPHA-(METHYLAMINOMETHYL)BENZYL ALCOHOL HYDROCHLORIDE
  • METANEPHRINE (HCL)
  • METANEPHRINE HYDROCHLORIDE
CAS:
881-95-8
MF:
C10H16ClNO3
MW:
233.69
EINECS:
212-922-2
Product Categories:
  • Intermediates & Fine Chemicals
  • Metabolites & Impurities
  • Standards - 13C & 2H for GC-Mass Spectrometry
  • Pharmaceuticals
Mol File:
881-95-8.mol
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DL-M-O-METHYLEPINEPHRINE HYDROCHLORIDE Chemical Properties

Melting point:
180-182?C
Density 
1.320 g/cm3
storage temp. 
2-8°C
solubility 
H2O: soluble
form 
powder
color 
white to off-white
Stability:
Hygroscopic
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-36
WGK Germany 
3
RTECS 
DA4798000

MSDS

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DL-M-O-METHYLEPINEPHRINE HYDROCHLORIDE Usage And Synthesis

Chemical Properties

Off-White to Pale Yellow Solid

Uses

A metabolite of Epinephrine (E588585). A naturraly occurring derivative of Epinephrine, found in urine and in certain tissues.

Biochem/physiol Actions

Metanephrine is an endogenous metabolite of ephinephrine, formed by catechol-O-methyl transferase activity. It is best known as a biomarker for cancers, as levels of free metanephrine are used to diagnose pheochromocytoma. Metanephrine was previously thought to be biologically inactive, but it is a more potent agonist at Trace amine associated receptor TAAR1 than either epinephrine or norepinephrine. Trace amine associated receptors (TAARs) are recently discovered GPCRs that are activated by endogenous trace amines (tyramine, tryptamine, synephrine, octopamine, β-phenylethylamine), which are chemically similar to monoaminergic neurotransmitters (epinephrine, norepinephrine, dopamine). Trace amines and TAARs are expressed in brain and are implicated in modulation of monoaminergic neurotransmission.

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