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Details

Stereochemistry RACEMIC
Molecular Formula C6H12O2
Molecular Weight 116.1583
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of GLYCIDYL ISOPROPYL ETHER

SMILES

CC(C)OCC1CO1

InChI

InChIKey=NWLUZGJDEZBBRH-UHFFFAOYSA-N
InChI=1S/C6H12O2/c1-5(2)7-3-6-4-8-6/h5-6H,3-4H2,1-2H3

HIDE SMILES / InChI
Molecular Formula C6H12O2
Molecular Weight 116.1583
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Approval Year

Unknown
149124
PubMed

PubMed

TitleDatePubMed
Modification of wood with isopropyl glycidyl ether and its effects on decay resistance and light stability.
2006-07
Substance Class Chemical
Created
by admin
on Mon Mar 31 21:45:03 GMT 2025
Edited
by admin
on Mon Mar 31 21:45:03 GMT 2025
Record UNII
1V3116630G
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
GLYCIDYL ISOPROPYL ETHER
Systematic Name English
NSC-4127
Preferred Name English
GLYCIDYL ISOPROPYL ETHER, (±)-
Systematic Name English
(ISOPROPOXYMETHYL)OXIRANE
Systematic Name English
2,3-EPOXYPROPYL-ISOPROPYL ETHER
Systematic Name English
ISOPROPYL EPOXYPROPYL ETHER
Systematic Name English
NSC-46562
Code English
2-(ISOPROPOXYMETHYL)OXIRANE
Systematic Name English
2,3-EPOXYPROPYL ISOPROPYL ETHER
Systematic Name English
(ISOPROPYLOXYMETHYL)OXIRANE
Systematic Name English
1,2-EPOXY-3-ISOPROPOXYPROPANE
Systematic Name English
OXIRANE, 2-((1-METHYLETHOXY)METHYL)-
Systematic Name English
OXIRANE, ((1-METHYLETHOXY)METHYL)-
Systematic Name English
3-ISOPROPOXY-1,2-EPOXYPROPANE
Systematic Name English
PROPANE, 1,2-EPOXY-3-ISOPROPOXY-
Systematic Name English
((1-METHYLETHOXY)METHYL)OXIRANE
Systematic Name English
2-((1-METHYLETHOXY)METHYL)OXIRANE
Systematic Name English
3-ISOPROPYLOXYPROPYLENE OXIDE
Systematic Name English
ISOPROPYL GLYCIDYL ETHER [HSDB]
Common Name English
Code System Code Type Description
FDA UNII
1V3116630G
Created by admin on Mon Mar 31 21:45:03 GMT 2025 , Edited by admin on Mon Mar 31 21:45:03 GMT 2025
PRIMARY
ECHA (EC/EINECS)
223-672-9
Created by admin on Mon Mar 31 21:45:03 GMT 2025 , Edited by admin on Mon Mar 31 21:45:03 GMT 2025
PRIMARY
HSDB
4302
Created by admin on Mon Mar 31 21:45:03 GMT 2025 , Edited by admin on Mon Mar 31 21:45:03 GMT 2025
PRIMARY
EPA CompTox
DTXSID6025480
Created by admin on Mon Mar 31 21:45:03 GMT 2025 , Edited by admin on Mon Mar 31 21:45:03 GMT 2025
PRIMARY
PUBCHEM
19920
Created by admin on Mon Mar 31 21:45:03 GMT 2025 , Edited by admin on Mon Mar 31 21:45:03 GMT 2025
PRIMARY
CAS
4016-14-2
Created by admin on Mon Mar 31 21:45:03 GMT 2025 , Edited by admin on Mon Mar 31 21:45:03 GMT 2025
PRIMARY
NSC
46562
Created by admin on Mon Mar 31 21:45:03 GMT 2025 , Edited by admin on Mon Mar 31 21:45:03 GMT 2025
PRIMARY
NSC
4127
Created by admin on Mon Mar 31 21:45:03 GMT 2025 , Edited by admin on Mon Mar 31 21:45:03 GMT 2025
PRIMARY
NIH
NCATS
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