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Details

Stereochemistry ACHIRAL
Molecular Formula C28H56O2
Molecular Weight 424.743
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of MYRISTYL MYRISTATE

SMILES

CCCCCCCCCCCCCCOC(=O)CCCCCCCCCCCCC

InChI

InChIKey=DZKXJUASMGQEMA-UHFFFAOYSA-N
InChI=1S/C28H56O2/c1-3-5-7-9-11-13-15-17-19-21-23-25-27-30-28(29)26-24-22-20-18-16-14-12-10-8-6-4-2/h3-27H2,1-2H3

HIDE SMILES / InChI

Molecular Formula C28H56O2
Molecular Weight 424.743
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Inactive ingredient
SYNALAR TS

Approved Use

SYNALAR solution is indicated for the relief of the inflammatory and pruritic manifestations of corticosteriod-responsive dermatoses.

Launch Date

2012
PubMed

PubMed

TitleDatePubMed
Online monitoring of biotransformations in high viscous multiphase systems by means of FT-IR and chemometrics.
2010-07-15
Fatty acyl-CoA reductase and wax synthase from Euglena gracilis in the biosynthesis of medium-chain wax esters.
2010-03
Substance Class Chemical
Created
by admin
on Mon Mar 31 18:50:58 GMT 2025
Edited
by admin
on Mon Mar 31 18:50:58 GMT 2025
Record UNII
4042ZC00DY
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
MYRISTYL MYRISTATE
INCI   VANDF  
INCI  
Official Name English
HALLSTAR MM
Preferred Name English
MACKADERM MM
Brand Name English
TETRADECANOIC ACID, TETRADECYL ESTER
Common Name English
MYRISTYL MYRISTATE [VANDF]
Common Name English
NIKKOL MM
Brand Name English
TETRADECYL TETRADECANOATE
Systematic Name English
TEGOSOFT MM
Brand Name English
PROTACHEM MM
Brand Name English
Code System Code Type Description
DAILYMED
4042ZC00DY
Created by admin on Mon Mar 31 18:50:58 GMT 2025 , Edited by admin on Mon Mar 31 18:50:58 GMT 2025
PRIMARY
SMS_ID
100000092919
Created by admin on Mon Mar 31 18:50:58 GMT 2025 , Edited by admin on Mon Mar 31 18:50:58 GMT 2025
PRIMARY
EVMPD
SUB28929
Created by admin on Mon Mar 31 18:50:58 GMT 2025 , Edited by admin on Mon Mar 31 18:50:58 GMT 2025
PRIMARY
CHEBI
138721
Created by admin on Mon Mar 31 18:50:58 GMT 2025 , Edited by admin on Mon Mar 31 18:50:58 GMT 2025
PRIMARY
CAS
3234-85-3
Created by admin on Mon Mar 31 18:50:58 GMT 2025 , Edited by admin on Mon Mar 31 18:50:58 GMT 2025
PRIMARY
PUBCHEM
18605
Created by admin on Mon Mar 31 18:50:58 GMT 2025 , Edited by admin on Mon Mar 31 18:50:58 GMT 2025
PRIMARY
RXCUI
1425924
Created by admin on Mon Mar 31 18:50:58 GMT 2025 , Edited by admin on Mon Mar 31 18:50:58 GMT 2025
PRIMARY RxNorm
EPA CompTox
DTXSID5047403
Created by admin on Mon Mar 31 18:50:58 GMT 2025 , Edited by admin on Mon Mar 31 18:50:58 GMT 2025
PRIMARY
FDA UNII
4042ZC00DY
Created by admin on Mon Mar 31 18:50:58 GMT 2025 , Edited by admin on Mon Mar 31 18:50:58 GMT 2025
PRIMARY
ECHA (EC/EINECS)
221-787-9
Created by admin on Mon Mar 31 18:50:58 GMT 2025 , Edited by admin on Mon Mar 31 18:50:58 GMT 2025
PRIMARY