harmine hydrochloride hydrate

9H-pyrido[3,4-b]indole, 7-methoxy-1-methyl-, hydrochloride (1:1)

CAS: 343-27-1 C13 H13 Cl N2 O MW: 248.71181000

Identification

Nameharmine hydrochloride hydrate
IUPAC7-methoxy-1-methyl-9H-pyrido[3,4-b]indole;hydrochloride
CAS Number343-27-1
EINECS206-443-8
FDA UNIIT89I34ODAA
Molecular FormulaC13 H13 Cl N2 O
Molecular Weight248.71181000
MDL NumberMFCD00012641

Regulatory

Physical Properties

Assay 95.00 to 100.00
Food Chemicals Codex Listed No
Melting Point 264.00 to 266.00 °C. @ 760.00 mm Hg
Boiling Point 421.40 °C. @ 760.00 mm Hg (est)
Vapor Pressure 0.000001 mmHg @ 25.00 °C. (est)
Flash Point 284.00 °F. TCC ( 139.80 °C. ) (est)
logP (o/w) 3.173 (est)
Soluble in water, 13.66 mg/L @ 25 °C (est)

No sensory data available

Safety Information

Preferred SDSView
Oral/Parenteral Toxicityintravenous-mouse LD50 38 mg/kg
Dermal ToxicityNot determined
Inhalation ToxicityNot determined

GHS Classification

['GHS Classification in accordance with 29 CFR 1910 (OSHA HCS)', 'GHS Label elements, including precautionary statements']

Safety in Use

Categorypharmaceuticals / chemical synthisis
Recommendation for harmine hydrochloride hydrate usage levels up tonot for fragrance use.
Recommendation for harmine hydrochloride hydrate flavor usage levels up tonot for flavor use.

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Potential Uses

None Found

Natural Occurrence

rue wild rue seeds

Synonyms

harmine hydrochloride harmine monohydrochloride harmine, hydrochloride 7- methoxy-1-methyl-9H-pyrido(3,4-b)indole hydrochloride 7- methoxy-1-methyl-9H-pyrido[3,4-b]indole hydrochloride 7- methoxy-1-methyl-9H-pyrido[3,4-b]indole;hydrochloride 7- methoxy-1-methylbeta-carboline, chloride 9H- pyrido(3,4-b)indole, 7-methoxy-1-methyl-, monohydrochloride 9H- pyrido[3,4-b]indole, 7-methoxy-1-methyl-, hydrochloride (1:1) 9H- pyrido[3,4-b]indole, 7-methoxy-1-methyl-, monohydrochloride PubMed: Harmine hydrochloride inhibits Akt phosphorylation and depletes the pool of cancer stem-like cells of glioblastoma. PubMed: Negative-mode MALDI mass spectrometry for the analysis of pigments using tetrathiafulvalene as a matrix. PubMed: Solid-phase fluorescence and ionization efficiency in negative-ion matrix-assisted laser desorption/ionization of neutral oligosaccharides: interaction between beta-carboline matrix and ammonium salt. PubMed: Structural features controlling the binding of beta-carbolines to the benzodiazepine receptor.