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(+)-Norfenfluramine hydrochloride_Molecular_structure_CAS_37936-89-3)
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(+)-Norfenfluramine hydrochloride

Catalog No. N3288 Name Sigma Aldrich
CAS Number 37936-89-3 Website http://www.sigmaaldrich.com
M. F. C10H13ClF3N Telephone 1-800-521-8956
M. W. 239.6651296 Fax
Purity ≥98% (HPLC) Email
Storage Chembase ID: 153158

SYNONYMS

Title
(+)-Norfenfluramine 盐酸盐
IUPAC name
(2S)-1-[3-(trifluoromethyl)phenyl]propan-2-amine hydrochloride
IUPAC Traditional name
(2S)-1-[3-(trifluoromethyl)phenyl]propan-2-amine hydrochloride
Synonyms
S-(+)-α-Methyl-3-(trifluoromethyl)benzeneethanamine hydrochloride
JP 92
S-(+)-α-Methyl-3-(trifluoromethyl)benzeneethanamine 盐酸盐
NSC 43036

DATABASE IDS

MDL Number MFCD11045299
CAS Number 37936-89-3

PROPERTIES

Empirical Formula (Hill Notation) C10H12F3N · HCl
Purity ≥98% (HPLC)
Apperance white powder
Solubility H2O: >10 mg/mL
GHS Pictograms GHS07
GHS Signal Word Warning
GHS Hazard statements H315-H319-H335
European Hazard Symbols Irritant Irritant (Xi)
MSDS Link Download
Personal Protective Equipment dust mask type N95 (US), Eyeshields, Gloves
GHS Precautionary statements P261-P305 + P351 + P338
Risk Statements 36/37/38
Safety Statements 26-36/37
Storage Temperature 2-8°C
German water hazard class 3

DETAILS

Description (English)
Biochem/physiol Actions
(+)-Norfenfluramine is the major hepatic metabolite of (+)-fenfluramine and is primarily responsible for the anorexic effect, as well as side effects; (+)-norfenfluramine causes vasoconstriction and a blood pressure increase in rats with normal blood; acts primarily on the cytoplasmic pool of serotonin; more potent than fenfluramine at inducing dopamine release.
Description (简体中文)
Biochem/physiol Actions
(+)-Norfenfluramine is the major hepatic metabolite of (+)-fenfluramine and is primarily responsible for the anorexic effect, as well as side effects; (+)-norfenfluramine causes vasoconstriction and a blood pressure increase in rats with normal blood; acts primarily on the cytoplasmic pool of serotonin; more potent than fenfluramine at inducing dopamine release.

REFERENCES