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Details

Stereochemistry ACHIRAL
Molecular Formula C12H22O4
Molecular Weight 230.3007
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of DIBUTYL SUCCINATE

SMILES

CCCCOC(=O)CCC(=O)OCCCC

InChI

InChIKey=YUXIBTJKHLUKBD-UHFFFAOYSA-N
InChI=1S/C12H22O4/c1-3-5-9-15-11(13)7-8-12(14)16-10-6-4-2/h3-10H2,1-2H3

HIDE SMILES / InChI

Molecular Formula C12H22O4
Molecular Weight 230.3007
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Dibutyl succinate is used as an insecticide, surfactant and insect attractant. Preliminary investigations have found that dibutyl succinate exhibits insulinotropic action on isolated islet cells suggesting that it may have some application for the treatment of diabetes.

Approval Year

Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Primary
Unknown

Approved Use

Unknown
PubMed

PubMed

TitleDatePubMed
Molecular structure of crude beeswax studied by solid-state 13C NMR.
2004
Patents

Sample Use Guides

In Vivo Use Guide
Unknown
Route of Administration: Unknown
In Vitro Use Guide
Groups of eight islets were each incubated for 90 min in 1.0 mL of a bicarbonate-buffered medium containing bovine serum albumin (5.0 mg/mL) and D-glucose (7.0 mM) and 10 mM of dibutyl succinate. The insulin released by the islets in the incubation medium was then assayed by a radioimmunological back titration. dibutyl succinate significantly augmented insulin release by +24.8 micor-U per in the 90 min incubation period.
Substance Class Chemical
Created
by admin
on Fri Dec 15 17:47:45 GMT 2023
Edited
by admin
on Fri Dec 15 17:47:45 GMT 2023
Record UNII
Q050512U41
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
DIBUTYL SUCCINATE
HSDB   MI  
Systematic Name English
NSC-1502
Code English
DIBUTYLSUCCINATE
Systematic Name English
DIBUTYL SUCCINATE [MI]
Common Name English
DIBUTYL SUCCINATE [HSDB]
Common Name English
DIBUTYL BUTANEDIOATE
Systematic Name English
Classification Tree Code System Code
WHO-VATC QP53GX03
Created by admin on Fri Dec 15 17:47:45 GMT 2023 , Edited by admin on Fri Dec 15 17:47:45 GMT 2023
EPA PESTICIDE CODE 77802
Created by admin on Fri Dec 15 17:47:45 GMT 2023 , Edited by admin on Fri Dec 15 17:47:45 GMT 2023
WHO-ATC P03BX04
Created by admin on Fri Dec 15 17:47:45 GMT 2023 , Edited by admin on Fri Dec 15 17:47:45 GMT 2023
Code System Code Type Description
MERCK INDEX
m143
Created by admin on Fri Dec 15 17:47:45 GMT 2023 , Edited by admin on Fri Dec 15 17:47:45 GMT 2023
PRIMARY Merck Index
FDA UNII
Q050512U41
Created by admin on Fri Dec 15 17:47:45 GMT 2023 , Edited by admin on Fri Dec 15 17:47:45 GMT 2023
PRIMARY
ALANWOOD
dibutyl succinate
Created by admin on Fri Dec 15 17:47:45 GMT 2023 , Edited by admin on Fri Dec 15 17:47:45 GMT 2023
PRIMARY
ChEMBL
CHEMBL1788388
Created by admin on Fri Dec 15 17:47:45 GMT 2023 , Edited by admin on Fri Dec 15 17:47:45 GMT 2023
PRIMARY
CAS
141-03-7
Created by admin on Fri Dec 15 17:47:45 GMT 2023 , Edited by admin on Fri Dec 15 17:47:45 GMT 2023
PRIMARY
HSDB
1563
Created by admin on Fri Dec 15 17:47:45 GMT 2023 , Edited by admin on Fri Dec 15 17:47:45 GMT 2023
PRIMARY
EPA CompTox
DTXSID7021998
Created by admin on Fri Dec 15 17:47:45 GMT 2023 , Edited by admin on Fri Dec 15 17:47:45 GMT 2023
PRIMARY
PUBCHEM
8830
Created by admin on Fri Dec 15 17:47:45 GMT 2023 , Edited by admin on Fri Dec 15 17:47:45 GMT 2023
PRIMARY
NSC
1502
Created by admin on Fri Dec 15 17:47:45 GMT 2023 , Edited by admin on Fri Dec 15 17:47:45 GMT 2023
PRIMARY
DRUG CENTRAL
4415
Created by admin on Fri Dec 15 17:47:45 GMT 2023 , Edited by admin on Fri Dec 15 17:47:45 GMT 2023
PRIMARY
ECHA (EC/EINECS)
205-449-8
Created by admin on Fri Dec 15 17:47:45 GMT 2023 , Edited by admin on Fri Dec 15 17:47:45 GMT 2023
PRIMARY
DRUG BANK
DB13332
Created by admin on Fri Dec 15 17:47:45 GMT 2023 , Edited by admin on Fri Dec 15 17:47:45 GMT 2023
PRIMARY
Related Record Type Details
ACTIVE MOIETY