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Details

Stereochemistry ABSOLUTE
Molecular Formula C12H24O2
Molecular Weight 200.3178
Optical Activity UNSPECIFIED
Defined Stereocenters 3 / 3
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 2-(L-MENTHOXY)ETHANOL

SMILES

CC(C)[C@@H]1CC[C@@H](C)C[C@H]1OCCO

InChI

InChIKey=FVBGFZNFXUIHNC-GRYCIOLGSA-N
InChI=1S/C12H24O2/c1-9(2)11-5-4-10(3)8-12(11)14-7-6-13/h9-13H,4-8H2,1-3H3/t10-,11+,12-/m1/s1

HIDE SMILES / InChI

Molecular Formula C12H24O2
Molecular Weight 200.3178
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 3 / 3
E/Z Centers 0
Optical Activity UNSPECIFIED

2-(L-MENTHOXY)ETHANOL is used as a food additive and it has been described as bland and odorless with a minty aroma. There are currently no safety concerns regarding the use of this compound (latest evaluation 2008). It belongs to the class of organic compounds known as menthane monoterpenoids.

Approval Year

Substance Class Chemical
Created
by admin
on Mon Mar 31 20:17:54 GMT 2025
Edited
by admin
on Mon Mar 31 20:17:54 GMT 2025
Record UNII
5ZWW23169H
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
COOLACT5
Preferred Name English
2-(L-MENTHOXY)ETHANOL
FHFI  
Common Name English
2-(L-MENTHOXY)ETHANOL [FHFI]
Common Name English
ETHANOL, 2-(((1R,2S,5R)-5-METHYL-2-(1-METHYLETHYL)CYCLOHEXYL)OXY)-
Systematic Name English
2-(LAEVO-MENTHOXY) ETHANOL
Common Name English
FEMA NO. 4154
Code English
2-((1R,2S,5R)-2-ISOPROPYL-5-METHYL-CYCLOHEXOXY)ETHANOL
Systematic Name English
ETHANOL, 2-((5-METHYL-2-(1-METHYLETHYL)CYCLOHEXYL)OXY)-, (1R-(1.ALPHA.,2.BETA.,5.ALPHA.))-
Common Name English
2-L-MENTHOXYETHANOL
Common Name English
Code System Code Type Description
PUBCHEM
10219851
Created by admin on Mon Mar 31 20:17:54 GMT 2025 , Edited by admin on Mon Mar 31 20:17:54 GMT 2025
PRIMARY
RXCUI
1428832
Created by admin on Mon Mar 31 20:17:54 GMT 2025 , Edited by admin on Mon Mar 31 20:17:54 GMT 2025
PRIMARY RxNorm
JECFA MONOGRAPH
1831
Created by admin on Mon Mar 31 20:17:54 GMT 2025 , Edited by admin on Mon Mar 31 20:17:54 GMT 2025
PRIMARY
CAS
75443-64-0
Created by admin on Mon Mar 31 20:17:54 GMT 2025 , Edited by admin on Mon Mar 31 20:17:54 GMT 2025
PRIMARY
DAILYMED
5ZWW23169H
Created by admin on Mon Mar 31 20:17:54 GMT 2025 , Edited by admin on Mon Mar 31 20:17:54 GMT 2025
PRIMARY
DRUG BANK
DB11174
Created by admin on Mon Mar 31 20:17:54 GMT 2025 , Edited by admin on Mon Mar 31 20:17:54 GMT 2025
PRIMARY
FDA UNII
5ZWW23169H
Created by admin on Mon Mar 31 20:17:54 GMT 2025 , Edited by admin on Mon Mar 31 20:17:54 GMT 2025
PRIMARY
Related Record Type Details
ACTIVE MOIETY