Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C6H14O3 |
| Molecular Weight | 134.1736 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CCOCCOCCO
InChI
InChIKey=XXJWXESWEXIICW-UHFFFAOYSA-N
InChI=1S/C6H14O3/c1-2-8-5-6-9-4-3-7/h7H,2-6H2,1H3
| Molecular Formula | C6H14O3 |
| Molecular Weight | 134.1736 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
Diethylene glycol monoethyl ether (under brand name Transcutol) is used as a vehicle in the formulation or manufacturing process of pharmaceuticals, cosmetics, and food additives. Transcutol is safe for use and has low irritancy inferred by numerous toxicological studies and precedence of use in approved topical medicines.
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Study of in vitro drug release and percutaneous absorption of fluconazole from topical dosage forms. | 2010-06 |
|
| Penetration enhancer-containing vesicles (PEVs) as carriers for cutaneous delivery of minoxidil. | 2009-10-01 |
|
| Homogeneous, surfactant-free gold nanoparticles encapsulated by polythiophene analogues. | 2009-04-21 |
|
| Airborne concentrations of volatile organic compounds, formaldehyde and ammonia in Finnish office buildings with suspected indoor air problems. | 2009-03 |
|
| The influence of cosurfactants and oils on the formation of pharmaceutical microemulsions based on PEG-8 caprylic/capric glycerides. | 2008-03-20 |
|
| Control of transdermal permeation of hydrocortisone acetate from hydrophilic and lipophilic formulations. | 2008 |
|
| Inhibition of hyaluronan export reduces collagen degradation in interleukin-1 treated cartilage. | 2008 |
|
| A GC/MS study of the drying of ballpoint pen ink on paper. | 2007-05-24 |
|
| In vitro and in vivo stability of caffeic acid phenethyl ester, a bioactive compound of propolis. | 2007-05-02 |
|
| An evaluation of the allelopathic potential of selected perennial groundcovers: foliar volatiles of catmint (Nepeta x faassenii) inhibit seedling growth. | 2006-08 |
|
| Biomonitoring of 2-(2-alkoxyethoxy)ethanols by analysing urinary 2-(2-alkoxyethoxy)acetic acids. | 2005-03-28 |
|
| Structure elucidation, synthesis, and contact allergenic activity of a major hydroperoxide formed at autoxidation of the ethoxylated surfactant C12E5. | 2003-05 |
|
| Enhanced skin permeation of a new capsaicin derivative (DA-5018) from a binary vehicle system composed of isopropyl myristate and ethoxydiglycol. | 2001-06 |
Patents
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 17:50:07 GMT 2025
by
admin
on
Mon Mar 31 17:50:07 GMT 2025
|
| Record UNII |
A1A1I8X02B
|
| Record Status |
Validated (UNII)
|
| Record Version |
|
-
Download
| Name | Type | Language | ||
|---|---|---|---|---|
|
Preferred Name | English | ||
|
Systematic Name | English | ||
|
Brand Name | English | ||
|
Common Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Code | English | ||
|
Systematic Name | English | ||
|
Brand Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Common Name | English |
| Classification Tree | Code System | Code | ||
|---|---|---|---|---|
|
EPA PESTICIDE CODE |
11504
Created by
admin on Mon Mar 31 17:50:07 GMT 2025 , Edited by admin on Mon Mar 31 17:50:07 GMT 2025
|
| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
|
1311147
Created by
admin on Mon Mar 31 17:50:07 GMT 2025 , Edited by admin on Mon Mar 31 17:50:07 GMT 2025
|
PRIMARY | RxNorm | ||
|
2-(2-ETHOXYETHOXY)ETHANOL
Created by
admin on Mon Mar 31 17:50:07 GMT 2025 , Edited by admin on Mon Mar 31 17:50:07 GMT 2025
|
PRIMARY | |||
|
111-90-0
Created by
admin on Mon Mar 31 17:50:07 GMT 2025 , Edited by admin on Mon Mar 31 17:50:07 GMT 2025
|
PRIMARY | |||
|
8146
Created by
admin on Mon Mar 31 17:50:07 GMT 2025 , Edited by admin on Mon Mar 31 17:50:07 GMT 2025
|
PRIMARY | |||
|
408451
Created by
admin on Mon Mar 31 17:50:07 GMT 2025 , Edited by admin on Mon Mar 31 17:50:07 GMT 2025
|
PRIMARY | |||
|
CHEMBL1230841
Created by
admin on Mon Mar 31 17:50:07 GMT 2025 , Edited by admin on Mon Mar 31 17:50:07 GMT 2025
|
PRIMARY | |||
|
C65380
Created by
admin on Mon Mar 31 17:50:07 GMT 2025 , Edited by admin on Mon Mar 31 17:50:07 GMT 2025
|
PRIMARY | |||
|
203-919-7
Created by
admin on Mon Mar 31 17:50:07 GMT 2025 , Edited by admin on Mon Mar 31 17:50:07 GMT 2025
|
PRIMARY | |||
|
C010111
Created by
admin on Mon Mar 31 17:50:07 GMT 2025 , Edited by admin on Mon Mar 31 17:50:07 GMT 2025
|
PRIMARY | |||
|
DTXSID2021941
Created by
admin on Mon Mar 31 17:50:07 GMT 2025 , Edited by admin on Mon Mar 31 17:50:07 GMT 2025
|
PRIMARY | |||
|
50
Created by
admin on Mon Mar 31 17:50:07 GMT 2025 , Edited by admin on Mon Mar 31 17:50:07 GMT 2025
|
PRIMARY | |||
|
SUB42639
Created by
admin on Mon Mar 31 17:50:07 GMT 2025 , Edited by admin on Mon Mar 31 17:50:07 GMT 2025
|
PRIMARY | |||
|
SUB11902MIG
Created by
admin on Mon Mar 31 17:50:07 GMT 2025 , Edited by admin on Mon Mar 31 17:50:07 GMT 2025
|
PRIMARY | |||
|
1193301
Created by
admin on Mon Mar 31 17:50:07 GMT 2025 , Edited by admin on Mon Mar 31 17:50:07 GMT 2025
|
PRIMARY | |||
|
m4404
Created by
admin on Mon Mar 31 17:50:07 GMT 2025 , Edited by admin on Mon Mar 31 17:50:07 GMT 2025
|
PRIMARY | Merck Index | ||
|
A1A1I8X02B
Created by
admin on Mon Mar 31 17:50:07 GMT 2025 , Edited by admin on Mon Mar 31 17:50:07 GMT 2025
|
PRIMARY | |||
|
C45678
Created by
admin on Mon Mar 31 17:50:07 GMT 2025 , Edited by admin on Mon Mar 31 17:50:07 GMT 2025
|
CONCEPT | Industrial Aid | ||
|
100000076096
Created by
admin on Mon Mar 31 17:50:07 GMT 2025 , Edited by admin on Mon Mar 31 17:50:07 GMT 2025
|
PRIMARY | |||
|
40572
Created by
admin on Mon Mar 31 17:50:07 GMT 2025 , Edited by admin on Mon Mar 31 17:50:07 GMT 2025
|
PRIMARY | |||
|
A1A1I8X02B
Created by
admin on Mon Mar 31 17:50:07 GMT 2025 , Edited by admin on Mon Mar 31 17:50:07 GMT 2025
|
PRIMARY |
| Related Record | Type | Details | ||
|---|---|---|---|---|
|
|
ACTIVE MOIETY |
|