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Details

Stereochemistry ACHIRAL
Molecular Formula C19H42N.HO
Molecular Weight 301.5508
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of CETRIMONIUM HYDROXIDE

SMILES

[OH-].CCCCCCCCCCCCCCCC[N+](C)(C)C

InChI

InChIKey=WJLUBOLDZCQZEV-UHFFFAOYSA-M
InChI=1S/C19H42N.H2O/c1-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20(2,3)4;/h5-19H2,1-4H3;1H2/q+1;/p-1

HIDE SMILES / InChI

Molecular Formula C19H42N
Molecular Weight 284.5435
Charge 1
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Molecular Formula HO
Molecular Weight 17.0073
Charge -1
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Description
Curator's Comment: Description was created based on several sources, including http://www.americanpharmaceuticalreview.com/Featured-Articles/38886-Antimicrobial-Preservatives-Part-One-Choosing-a-Preservative-System/ | https://books.google.ru/books?id=EMrSBwAAQBAJ&printsec=frontcover&hl=ru#v=onepage&q&f=false | https://www.ncbi.nlm.nih.gov/pubmed/9880479 | http://www.medindia.net/doctors/drug_information/cetrimide.htm

Cetrimide is a quaternary ammonium compound. Cetrimide was first introduced as a combined cleanser and skin antiseptic by Barnes (1942). Cetrimide combines excellent detergent properties and minimal toxicity with a useful antiseptic action. Cetrimide affects membrane permeability allowing ‘leaking’ of essential cell constituents leading to cell death. This medication is a skin antiseptic and disinfectant prescribed for seborrhoeic dermatitis and wound cleansing. The cream has a bactericidal activity against gram-positive bacteria and incompatible with soaps and other anionic surfactants.

Originator

Curator's Comment: Cetrimide was first introduced as a combined cleanser and skin antiseptic by Barnes (1942). http://www.sciencedirect.com/science/article/pii/S0140673600701000 reference retrieved from https://www.ncbi.nlm.nih.gov/pubmed/18132350

Approval Year

TargetsConditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Curative
CETRIMIDE

Approved Use

Cetrimide is a skin antiseptic and disinfectant prescribed for seborrhoeic dermatitis and wound cleansing. The cream has a bactericidal activity against gram-positive bacteria and incompatible with soaps and other anionic surfactants.
Primary
CETRIMIDE

Approved Use

Cetrimide is a skin antiseptic and disinfectant prescribed for seborrhoeic dermatitis and wound cleansing. The cream has a bactericidal activity against gram-positive bacteria and incompatible with soaps and other anionic surfactants.
PubMed

PubMed

TitleDatePubMed
The effects of two quaternary ammonium compounds on citric acid and sterol synthesis in Aspergillus niger.
1963 Apr
Antiseptics and disinfectants: activity, action, and resistance.
1999 Jan
Patents

Sample Use Guides

Wound cleansing - Topical : Adult: Apply 0.1-1% aqueous solution or 0.5% cream onto affected area. Seborrhoeic dermatitis - Topical : Adult: Apply 10% shampoo solution onto the scalp.
Route of Administration: Topical
Cetrimide, at 30 ug/ml inhibited growth of Aspergillus niger.
Substance Class Chemical
Created
by admin
on Sat Dec 16 09:39:50 GMT 2023
Edited
by admin
on Sat Dec 16 09:39:50 GMT 2023
Record UNII
8Q7D6895LV
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
CETRIMONIUM HYDROXIDE
Common Name English
1-HEXADECANAMINIUM, N,N,N-TRIMETHYL-, HYDROXIDE (1:1)
Systematic Name English
CETRIMIDE [JAN]
Common Name English
AMMONIUM, HEXADECYLTRIMETHYL-, HYDROXIDE
Systematic Name English
CETYLTRIMETHYLAMMONIUM HYDROXIDE
Systematic Name English
1-HEXADECANAMINIUM, N,N,N-TRIMETHYL-, HYDROXIDE
Systematic Name English
HEXADECYLTRIMETHYLAMMONIUM HYDROXIDE
Systematic Name English
TRIMETHYLHEXADECYLAMMONIUM HYDROXIDE
Systematic Name English
Code System Code Type Description
PUBCHEM
68166
Created by admin on Sat Dec 16 09:39:50 GMT 2023 , Edited by admin on Sat Dec 16 09:39:50 GMT 2023
PRIMARY
ECHA (EC/EINECS)
208-022-4
Created by admin on Sat Dec 16 09:39:50 GMT 2023 , Edited by admin on Sat Dec 16 09:39:50 GMT 2023
PRIMARY
FDA UNII
8Q7D6895LV
Created by admin on Sat Dec 16 09:39:50 GMT 2023 , Edited by admin on Sat Dec 16 09:39:50 GMT 2023
PRIMARY
EPA CompTox
DTXSID40883410
Created by admin on Sat Dec 16 09:39:50 GMT 2023 , Edited by admin on Sat Dec 16 09:39:50 GMT 2023
PRIMARY
DRUG BANK
DBSALT001771
Created by admin on Sat Dec 16 09:39:50 GMT 2023 , Edited by admin on Sat Dec 16 09:39:50 GMT 2023
PRIMARY
CAS
505-86-2
Created by admin on Sat Dec 16 09:39:50 GMT 2023 , Edited by admin on Sat Dec 16 09:39:50 GMT 2023
PRIMARY
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