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Details

Stereochemistry RACEMIC
Molecular Formula C8H14N4O7
Molecular Weight 278.2194
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of N-(1,3-BIS(HYDROXYMETHYL)-2,5-DIOXO-4-IMIDAZOLIDINYL)-N,N'-BIS(HYDROXYMETHYL)UREA

SMILES

OCNC(=O)N(CO)C1N(CO)C(=O)N(CO)C1=O

InChI

InChIKey=SOROIESOUPGGFO-UHFFFAOYSA-N
InChI=1S/C8H14N4O7/c13-1-9-7(18)10(2-14)5-6(17)12(4-16)8(19)11(5)3-15/h5,13-16H,1-4H2,(H,9,18)

HIDE SMILES / InChI

Molecular Formula C8H14N4O7
Molecular Weight 278.2194
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Diazolidinylurea is a broad-spectrum antimicrobial preservative used in cosmetics and pharmaceutical preparations. It is especially active against gram-negative bacteria and is often combined with parabens. Diazolidinylurea is the most active member of the imidazolidinyl urea group, that acts as a formaldehyde releasers. Diazolidinylurea is used in many cosmetics, skin care products, shampoos, and conditioners, as well as a wide range of products including bubble baths, baby wipes, and household detergents.

Approval Year

Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Inactive ingredient
Pain Relief Cream by ALLURE LABS INC.

Approved Use

Topical Analgesic Uses: For the temporary relief of minor aches and pains of muscles and joints associated with arthritis, simple backache, strains, sprains and bruises.

Launch Date

2017
Doses

Doses

DosePopulationAdverse events​
6000 mg/m2 single, topical
Highest studied dose
Dose: 6000 mg/m2
Route: topical
Route: single
Dose: 6000 mg/m2
Sources:
unhealthy, ADULT
Health Status: unhealthy
Age Group: ADULT
Sex: M+F
Food Status: UNKNOWN
Sources:
PubMed

PubMed

TitleDatePubMed
ROAT: morphology of ROAT on arm, neck and face in formaldehyde and diazolidinyl urea sensitive individuals.
2006-01
[Contact sensitization to pharmaceutic aids in dermatologic cosmetic and external use preparations].
2004-05
Substance Class Chemical
Created
by admin
on Mon Mar 31 18:50:22 GMT 2025
Edited
by admin
on Mon Mar 31 18:50:22 GMT 2025
Record UNII
N9VX1IBW6K
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
N,N'-BIS(HYDROXYMETHYL)-N'-(1,3-BIS(HYDROXYMETHYL)-2,5-DIOXO-4-IMIDAZOLIDINYL)UREA
Preferred Name English
N-(1,3-BIS(HYDROXYMETHYL)-2,5-DIOXO-4-IMIDAZOLIDINYL)-N,N'-BIS(HYDROXYMETHYL)UREA
Systematic Name English
UREA, N-(1,3-BIS(HYDROXYMETHYL)-2,5-DIOXO-4-IMIDAZOLIDINYL)-N,N'-BIS(HYDROXYMETHYL)-
Systematic Name English
N-HYDROXYMETHYL-N-(1,3-DI(HYDROXYMETHYL)-2,5-DIOXOIMIDAZOLIDIN-4-YL)-N'-HYDROXY-METHYLUREA
Systematic Name English
Classification Tree Code System Code
EPA PESTICIDE CODE 128971
Created by admin on Mon Mar 31 18:50:22 GMT 2025 , Edited by admin on Mon Mar 31 18:50:22 GMT 2025
Code System Code Type Description
RXCUI
1990423
Created by admin on Mon Mar 31 18:50:22 GMT 2025 , Edited by admin on Mon Mar 31 18:50:22 GMT 2025
PRIMARY
FDA UNII
N9VX1IBW6K
Created by admin on Mon Mar 31 18:50:22 GMT 2025 , Edited by admin on Mon Mar 31 18:50:22 GMT 2025
PRIMARY
DAILYMED
N9VX1IBW6K
Created by admin on Mon Mar 31 18:50:22 GMT 2025 , Edited by admin on Mon Mar 31 18:50:22 GMT 2025
PRIMARY
PUBCHEM
62277
Created by admin on Mon Mar 31 18:50:22 GMT 2025 , Edited by admin on Mon Mar 31 18:50:22 GMT 2025
PRIMARY
EPA CompTox
DTXSID0029559
Created by admin on Mon Mar 31 18:50:22 GMT 2025 , Edited by admin on Mon Mar 31 18:50:22 GMT 2025
PRIMARY
ECHA (EC/EINECS)
278-928-2
Created by admin on Mon Mar 31 18:50:22 GMT 2025 , Edited by admin on Mon Mar 31 18:50:22 GMT 2025
PRIMARY
CAS
78491-02-8
Created by admin on Mon Mar 31 18:50:22 GMT 2025 , Edited by admin on Mon Mar 31 18:50:22 GMT 2025
PRIMARY