盐酸丙嗪

Description

promazine hydrochloride · CAS 53-60-1 · C17H21ClN2S. UNII U16EOR79U4.

Identification

CAS Registry Number	53-60-1
PubChem CID	5887
Molecular formula	C17H21ClN2S
IUPAC name	N,N-dimethyl-3-phenothiazin-10-ylpropan-1-amine;hydrochloride
UNII (FDA)	U16EOR79U4

Computed Descriptors

Molecular Weight	320.9
Hydrogen Bond Donor Count	1
Hydrogen Bond Acceptor Count	3
Rotatable Bond Count	4
Exact Mass	320.1113975
Monoisotopic Mass	320.1113975
Topological Polar Surface Area	31.8
Heavy Atom Count	21
Formal Charge	0
Complexity	285

Physical description & handling notes

• >48.1 [ug/mL] (The mean of the results at pH 7.4)
• 161.4 Ų [M+H]+ [CCS Type: TW; Method: calibrated with polyalanine and drug standards]

GHS Hazard Classification

Reported hazard statements	H302 (100%), H317 (97.6%)

Documented Uses

• Used as an adjunct for short term treatment of moderate and severe psychomotor agitation. Also used to treat agitation or restlessness in the elderly.
• Animal Drugs -> FDA Approved Animal Drug Products (Green Book) -> Active Ingredients
• 10H-Phenothiazine-10-propanamine, N,N-dimethyl-, hydrochloride (1:1): INACTIVE
• Drugs used to prevent NAUSEA or VOMITING.
• Agents that control agitated psychotic behavior, alleviate acute psychotic states, reduce psychotic symptoms, and exert a quieting effect. They are used in SCHIZOPHRENIA; senile dementia; transient psychosis following surgery; or MYOCARDIAL INFARCTION; etc. These drugs are often referred to as neuroleptics alluding to the tendency to produce neurological side effects, but not all antipsychotics are likely to produce such effects. Many of these drugs may also be effective against nausea, emesis, and pruritus.
• Hepatic, primarily to N-desmethylpromazine and promazine sulfoxide. Absorption may be erratic and peak plasma concentrations show large interindividual differences. The metabolism occurs through oxidative processes mediated largely by hepatic microsomal and other drug metabolizing enzymes. Antoher step is the conjugaion with glucuronic acid. Other reactions include hydroxylation, demetylation, and sulfoxide formation. Moreover, metabolic alterations in side chain may also occur (A308, A631).

Synonyms

PROMAZINE HYDROCHLORIDE; 53-60-1; Promazine Hcl; Starazin; Talofen; DTXSID4046949; NSC-17468; 10-(gamma-Dimethylamino-n-propyl)phenothiazine hydrochloride; U16EOR79U4; 10H-Phenothiazine-10-propanamine, N,N-dimethyl-, monohydrochloride; Promazine hydrochloride (USP); Promazine hydrochloride [USP]; 10-(3-(Dimethylamino)propyl)phenothiazine monohydrochloride; DTXCID2026949; NSC17468; CHEBI:8460

Frequently Asked Questions

What are the CAS number and molecular formula of promazine hydrochloride?

CAS 53-60-1; molecular formula C17H21ClN2S; molecular weight — g/mol.

What other names is promazine hydrochloride known by?

PROMAZINE HYDROCHLORIDE, 53-60-1, Promazine Hcl, Starazin, Talofen, DTXSID4046949.

Is promazine hydrochloride classified as hazardous?

Hazard statements reported: H302, H317.

Facts on this page are taken from PubChem (US National Library of Medicine) and Wikidata. Grade-specific data — assay, moisture, particle size, packaging, shelf life — is issued per batch on the COA and is not published here.