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Details

Stereochemistry ACHIRAL
Molecular Formula 2C12H23O2.C8H18Sn
Molecular Weight 631.558
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of DIBUTYLTIN DILAURATE

SMILES

CCCC[Sn++]CCCC.CCCCCCCCCCCC([O-])=O.CCCCCCCCCCCC([O-])=O

InChI

InChIKey=UKLDJPRMSDWDSL-UHFFFAOYSA-L
InChI=1S/2C12H24O2.2C4H9.Sn/c2*1-2-3-4-5-6-7-8-9-10-11-12(13)14;2*1-3-4-2;/h2*2-11H2,1H3,(H,13,14);2*1,3-4H2,2H3;/q;;;;+2/p-2

HIDE SMILES / InChI

Molecular Formula C8H18Sn
Molecular Weight 232.939
Charge 2
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Molecular Formula C12H23O2
Molecular Weight 199.3098
Charge -1
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Description
Curator's Comment: description was created based on several sources, including https://www.ncbi.nlm.nih.gov/pubmed/893325 | https://www.ncbi.nlm.nih.gov/pubmed/425288 | https://www.ncbi.nlm.nih.gov/pubmed/7261948 | https://www.ncbi.nlm.nih.gov/pubmed/4001047

Dibutyltin dilaurate (DBTDL) is an organotin compound that is used as a catalyst for polyurethane production from isocyanates and diols. Dibutyltin dilaurate improves the drying of chemically curing systems favoring the isocyanate/polyol reaction over other side reactions such as isocyanate/water. DBTL can be used to aid the curing process of polyurethanes, silicone resins, RTV silicone resins and silane modified polymers. Dibutyltin dilaurate was used for the removal of large roundworms, cecal worms, and several species of tapeworms from chickens and turkeys. Based on animal studies, prolonged or repeated overexposure to Dibutyltin dilaurate may affect the developing fetus, blood, and thymus. Overexposure to Dibutyltin dilaurate may also cause central nervous system effects.

Approval Year

Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Primary
Unknown

Approved Use

Unknown
PubMed

PubMed

TitleDatePubMed
Patents

Patents

Sample Use Guides

Rats were intragastrically administered 5, 10, or 20 mg/kg dibutyltin dilaurate to model sub-chronic poisoning.
Route of Administration: Oral
In Vitro Use Guide
Unknown
Substance Class Chemical
Created
by admin
on Fri Dec 15 14:59:36 GMT 2023
Edited
by admin
on Fri Dec 15 14:59:36 GMT 2023
Record UNII
L4061GMT90
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
DIBUTYLTIN DILAURATE
GREEN BOOK   HSDB   MI  
Systematic Name English
DIBUTYLBIS(LAUROYLOXY)TIN
Systematic Name English
DIBUTYLTINDILAURATE
Common Name English
DIBUTYLTIN DILAURATE [MI]
Common Name English
BUTYNORATE
Common Name English
TINOSTAT
Brand Name English
STANCLERE TL
Brand Name English
NSC-2607
Code English
TL-10
Common Name English
DIBUTYLTIN DILAURATE [HSDB]
Common Name English
DIBUTYLBIS((1-OXODODECYL)OXY)STANNANE
Systematic Name English
DIBUTYLTIN DILAURATE [GREEN BOOK]
Common Name English
DAVAINEX
Brand Name English
DESMORAPID Z
Brand Name English
DODECANOIC ACID 1,1'-(DIBUTYLSTANNYLENE) ESTER
Common Name English
Classification Tree Code System Code
WHO-VATC QP52AX04
Created by admin on Fri Dec 15 14:59:36 GMT 2023 , Edited by admin on Fri Dec 15 14:59:36 GMT 2023
Code System Code Type Description
NSC
2607
Created by admin on Fri Dec 15 14:59:36 GMT 2023 , Edited by admin on Fri Dec 15 14:59:36 GMT 2023
PRIMARY
RXCUI
2183100
Created by admin on Fri Dec 15 14:59:36 GMT 2023 , Edited by admin on Fri Dec 15 14:59:36 GMT 2023
PRIMARY
MESH
C010409
Created by admin on Fri Dec 15 14:59:36 GMT 2023 , Edited by admin on Fri Dec 15 14:59:36 GMT 2023
PRIMARY
MERCK INDEX
m4317
Created by admin on Fri Dec 15 14:59:36 GMT 2023 , Edited by admin on Fri Dec 15 14:59:36 GMT 2023
PRIMARY Merck Index
PUBCHEM
9809426
Created by admin on Fri Dec 15 14:59:36 GMT 2023 , Edited by admin on Fri Dec 15 14:59:36 GMT 2023
PRIMARY
HSDB
5214
Created by admin on Fri Dec 15 14:59:36 GMT 2023 , Edited by admin on Fri Dec 15 14:59:36 GMT 2023
PRIMARY
WIKIPEDIA
Dibutyltin dilaurate
Created by admin on Fri Dec 15 14:59:36 GMT 2023 , Edited by admin on Fri Dec 15 14:59:36 GMT 2023
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CAS
77-58-7
Created by admin on Fri Dec 15 14:59:36 GMT 2023 , Edited by admin on Fri Dec 15 14:59:36 GMT 2023
PRIMARY
EPA CompTox
DTXSID6024961
Created by admin on Fri Dec 15 14:59:36 GMT 2023 , Edited by admin on Fri Dec 15 14:59:36 GMT 2023
PRIMARY
ECHA (EC/EINECS)
201-039-8
Created by admin on Fri Dec 15 14:59:36 GMT 2023 , Edited by admin on Fri Dec 15 14:59:36 GMT 2023
PRIMARY
FDA UNII
L4061GMT90
Created by admin on Fri Dec 15 14:59:36 GMT 2023 , Edited by admin on Fri Dec 15 14:59:36 GMT 2023
PRIMARY
DAILYMED
L4061GMT90
Created by admin on Fri Dec 15 14:59:36 GMT 2023 , Edited by admin on Fri Dec 15 14:59:36 GMT 2023
PRIMARY
Related Record Type Details
PARENT -> SALT/SOLVATE