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N,N,beta-Trimethyl-10H-phenothiazine-10-ethanamine

HCID 110669
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Basic information

CAS
303-14-0
Standard SMILES
CC(CN(C)C)N1c2ccccc2Sc2ccccc21
InChIKey
CGNHCKZJGQDWBG-UHFFFAOYSA-N
Molecular formula
C17H20N2S
Average molar mass
284.4 g/mol
Monoisotopic mass
284.13471982

Overview

Isopromethazine is a member of phenothiazines.

Names & identifiers

Preferred name
N,N,beta-Trimethyl-10H-phenothiazine-10-ethanamine
IUPAC
N,N-dimethyl-2-phenothiazin-10-ylpropan-1-amine
English name
Isopromethazine
Molecular formula
C17H20N2S
Molecular weight
284.42

Names & synonyms

Isopromethazine303-14-0IsomethazineFen-BridalProthiazinN,N,beta-Trimethyl-10H-phenothiazine-10-ethanamine10-(2-Dimethylaminoisopropyl)phenothiazine044033O3TYLILLY-01526RP-4460RefChem:149784Isophenergan
Show more names
Promethazine hydrochloride impurity Bdimethyl(2-phenothiazin-10-ylpropyl)amineN,N,β-Trimethyl-10H-phenothiazine-10-ethanamine10H-Phenothiazine-10-ethanamine,N,N,b-trimethyl-N,N-dimethyl-2-phenothiazin-10-yl-propan-1-amine10-(2-Dimethylamino-1-methylethyl)-10H-phenothiazine
Promethazine EP Impurity BN,N-dimethyl-2-phenothiazin-10-ylpropan-1-aminedimethyl[2-(10H-phenothiazin-10-yl)propyl]amineN,N-dimethyl-2-(10H-phenothiazin-10-yl)propan-1-amineLilly 01526UNII-044033O3TYRP 3389ISOPROMETHAZINE [MI]

Database identifiers

CAS
303-14-0
PubChem CID
110669
DTXSID
DTXSID10952662
ChEBI

Properties

Computed structural properties

XLogP
4.2
Topological polar surface area
31.8 Ų
Hydrogen bond donors
0
Hydrogen bond acceptors
3
Rotatable bonds
3
Heavy atoms
20
Formal charge
0
Complexity
298

Physicochemical properties

Melting point
62 · 62-64 °C
Boiling point
224 · 224-225 °C(Press: 11 Torr)
Density
1.142 · 1.142±0.06 g/cm3(Temp: 25 °C; Press: 760 Torr)(predicted)
solubility
Chloroform (Slightly), Methanol (Slightly, Sonicated)
form
Solid
pka
8.948 · 8.948±0.28(predicted)
color
Pale Beige to Pale Brown
FDA UNII
44033 O3TY · 044033O3TY

Chemistry & industry

Pharmacology

MeSH Pharmacological Classification · 3 items

Agents, usually topical, that relieve itching (pruritus).

Drugs that selectively bind to but do not activate histamine H1 receptors, thereby blocking the actions of endogenous histamine. Included here are the classical antihistaminics that antagonize or prevent the action of histamine mainly in immediate hypersensitivity. They act in the bronchi, capillaries, and some other smooth muscles, and are used to prevent or allay motion sickness, seasonal rhinitis, and allergic dermatitis and to induce somnolence. The effects of blocking central nervous system H1 receptors are not as well understood.

Agents that are used to treat allergic reactions. Most of these drugs act by preventing the release of inflammatory mediators or inhibiting the actions of released mediators on their target cells. (From AMA Drug Evaluations Annual, 1994, p475)

Applications

UsesIsopromethazine is an impurity of Promethazine (P757000), an antihistamine used as an central nervous system depressant.

Additional notes

DefinitionChEBI: Isopromethazine is a member of phenothiazines.

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Compound notes

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On this pageBasic informationOverviewNames & identifiersPropertiesChemistry & industryRelated reactionsCompound notes
CHEBI:135176
UNII
044033O3TY
EC Number
608-457-3
Nikkaji
J5.487I