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Details

Stereochemistry RACEMIC
Molecular Formula C13H22O2
Molecular Weight 210.3126
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of LINALYL PROPIONATE

SMILES

CCC(=O)OC(C)(CCC=C(C)C)C=C

InChI

InChIKey=WAQIIHCCEMGYKP-UHFFFAOYSA-N
InChI=1S/C13H22O2/c1-6-12(14)15-13(5,7-2)10-8-9-11(3)4/h7,9H,2,6,8,10H2,1,3-5H3

HIDE SMILES / InChI

Molecular Formula C13H22O2
Molecular Weight 210.3126
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Approval Year

PubMed

PubMed

TitleDatePubMed
Fragrance material review on linalyl propionate.
2003-07
Variation of major volatile constituents in various green teas from Southeast Asia.
2001-03
Substance Class Chemical
Created
by admin
on Mon Mar 31 19:02:30 GMT 2025
Edited
by admin
on Mon Mar 31 19:02:30 GMT 2025
Record UNII
BI845A018T
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
FEMA NO. 2645
Preferred Name English
LINALYL PROPIONATE
FCC   FHFI  
Systematic Name English
(±)-LINALYL PROPIONATE
Systematic Name English
LINALYL PROPIONATE [FCC]
Common Name English
PROPIONIC ACID, LINALYL ESTER
Common Name English
1,6-OCTADIEN-3-OL, 3,7-DIMETHYL-, 3-PROPANOATE
Systematic Name English
LINALOOL PROPIONATE
Systematic Name English
3,7-DIMETHYLOCTA-1,6-DIEN-3-YL PROPANOATE
Systematic Name English
1,6-OCTADIEN-3-OL, 3,7-DIMETHYL-, PROPANOATE
Systematic Name English
1,6-OCTADIEN-3-OL, 3,7-DIMETHYL-, PROPIONATE
Systematic Name English
LINALYL PROPANOATE
Systematic Name English
LINALYL PROPIONATE [FHFI]
Common Name English
NSC-46139
Code English
Classification Tree Code System Code
JECFA EVALUATION LINALYL PROPIONATE
Created by admin on Mon Mar 31 19:02:30 GMT 2025 , Edited by admin on Mon Mar 31 19:02:30 GMT 2025
CFR 21 CFR 172.515
Created by admin on Mon Mar 31 19:02:30 GMT 2025 , Edited by admin on Mon Mar 31 19:02:30 GMT 2025
Code System Code Type Description
FDA UNII
BI845A018T
Created by admin on Mon Mar 31 19:02:30 GMT 2025 , Edited by admin on Mon Mar 31 19:02:30 GMT 2025
PRIMARY
PUBCHEM
61098
Created by admin on Mon Mar 31 19:02:30 GMT 2025 , Edited by admin on Mon Mar 31 19:02:30 GMT 2025
PRIMARY
EPA CompTox
DTXSID1047574
Created by admin on Mon Mar 31 19:02:30 GMT 2025 , Edited by admin on Mon Mar 31 19:02:30 GMT 2025
PRIMARY
ECHA (EC/EINECS)
205-627-5
Created by admin on Mon Mar 31 19:02:30 GMT 2025 , Edited by admin on Mon Mar 31 19:02:30 GMT 2025
PRIMARY
NSC
46139
Created by admin on Mon Mar 31 19:02:30 GMT 2025 , Edited by admin on Mon Mar 31 19:02:30 GMT 2025
PRIMARY
JECFA MONOGRAPH
361
Created by admin on Mon Mar 31 19:02:30 GMT 2025 , Edited by admin on Mon Mar 31 19:02:30 GMT 2025
PRIMARY
CAS
144-39-8
Created by admin on Mon Mar 31 19:02:30 GMT 2025 , Edited by admin on Mon Mar 31 19:02:30 GMT 2025
PRIMARY