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Details

Stereochemistry ABSOLUTE
Molecular Formula C18H36O6
Molecular Weight 348.4748
Optical Activity UNSPECIFIED
Defined Stereocenters 5 / 5
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of LAURYL GLUCOSIDE

SMILES

CCCCCCCCCCCCO[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O

InChI

InChIKey=PYIDGJJWBIBVIA-UYTYNIKBSA-N
InChI=1S/C18H36O6/c1-2-3-4-5-6-7-8-9-10-11-12-23-18-17(22)16(21)15(20)14(13-19)24-18/h14-22H,2-13H2,1H3/t14-,15-,16+,17-,18-/m1/s1

HIDE SMILES / InChI

Molecular Formula C18H36O6
Molecular Weight 348.4748
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 5 / 5
E/Z Centers 0
Optical Activity UNSPECIFIED

Lauryl glucoside is a non-ionic biodegradable surfactant made from plants; it is a member of the alkyl glucoside group and is used in cleaning agents and emulsions in cosmetics. Lauryl glucoside can lead to the allergic reactions.

Approval Year

Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
PubMed

PubMed

TitleDatePubMed
Patents

Sample Use Guides

In Vivo Use Guide
Unknown
Route of Administration: Unknown
In Vitro Use Guide
Unknown
Substance Class Chemical
Created
by admin
on Fri Dec 15 18:32:20 UTC 2023
Edited
by admin
on Fri Dec 15 18:32:20 UTC 2023
Record UNII
76LN7P7UCU
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
LAURYL GLUCOSIDE
INCI  
INCI  
Official Name English
LAURYL GLUCOSIDE [INCI]
Common Name English
DODECYL D-GLUCOSIDE
Common Name English
GLUCOSIDE, DODECYL, D-
Common Name English
D-GLUCOPYRANOSIDE, DODECYL
Common Name English
.BETA.-D-GLUCOPYRANOSIDE, DODECYL
Systematic Name English
DODECYL .BETA.-D-GLUCOPYRANOSIDE
Systematic Name English
Code System Code Type Description
WIKIPEDIA
LAURYL GLUCOSIDE
Created by admin on Fri Dec 15 18:32:20 UTC 2023 , Edited by admin on Fri Dec 15 18:32:20 UTC 2023
PRIMARY
CAS
59122-55-3
Created by admin on Fri Dec 15 18:32:20 UTC 2023 , Edited by admin on Fri Dec 15 18:32:20 UTC 2023
PRIMARY
RXCUI
1364382
Created by admin on Fri Dec 15 18:32:20 UTC 2023 , Edited by admin on Fri Dec 15 18:32:20 UTC 2023
PRIMARY RxNorm
PUBCHEM
93321
Created by admin on Fri Dec 15 18:32:20 UTC 2023 , Edited by admin on Fri Dec 15 18:32:20 UTC 2023
PRIMARY
DRUG BANK
DB14746
Created by admin on Fri Dec 15 18:32:20 UTC 2023 , Edited by admin on Fri Dec 15 18:32:20 UTC 2023
PRIMARY
EPA CompTox
DTXSID30893048
Created by admin on Fri Dec 15 18:32:20 UTC 2023 , Edited by admin on Fri Dec 15 18:32:20 UTC 2023
PRIMARY
ECHA (EC/EINECS)
248-685-7
Created by admin on Fri Dec 15 18:32:20 UTC 2023 , Edited by admin on Fri Dec 15 18:32:20 UTC 2023
NON-SPECIFIC STEREOCHEMISTRY
FDA UNII
76LN7P7UCU
Created by admin on Fri Dec 15 18:32:20 UTC 2023 , Edited by admin on Fri Dec 15 18:32:20 UTC 2023
PRIMARY
EVMPD
SUB172268
Created by admin on Fri Dec 15 18:32:20 UTC 2023 , Edited by admin on Fri Dec 15 18:32:20 UTC 2023
PRIMARY
ECHA (EC/EINECS)
261-614-4
Created by admin on Fri Dec 15 18:32:20 UTC 2023 , Edited by admin on Fri Dec 15 18:32:20 UTC 2023
PRIMARY
CAS
27836-64-2
Created by admin on Fri Dec 15 18:32:20 UTC 2023 , Edited by admin on Fri Dec 15 18:32:20 UTC 2023
NON-SPECIFIC STEREOCHEMISTRY
SMS_ID
100000160470
Created by admin on Fri Dec 15 18:32:20 UTC 2023 , Edited by admin on Fri Dec 15 18:32:20 UTC 2023
PRIMARY
DAILYMED
76LN7P7UCU
Created by admin on Fri Dec 15 18:32:20 UTC 2023 , Edited by admin on Fri Dec 15 18:32:20 UTC 2023
PRIMARY
Related Record Type Details
ACTIVE MOIETY