DIBUTYLTIN DILAURATE

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 Search

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
Sources: https://www.ncbi.nlm.nih.gov/pubmed/25538742
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.

CNS Activity

Originator

Approval Year

Conditions

Condition	Modality	Targets	Highest Phase	Product
Parasitic infectious disease 4 Sources: https://www.ncbi.nlm.nih.gov/pubmed/893325	Primary		Approved 8583	Unknown Approved Use Unknown

PubMed

Title	Date	PubMed
A plastic stabilizer dibutyltin dilaurate induces subchronic neurotoxicity in rats.	2012-10-05	25538742

Patents

Sample Use Guides

In Vivo Use Guide

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 `Mon Mar 31 17:34:22 GMT 2025` Edited by `admin` on `Mon Mar 31 17:34:22 GMT 2025`
Record UNII	L4061GMT90
Record Status	`Validated (UNII)`
Record Version

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Name

Type

Language

DIBUTYLTIN DILAURATE

Systematic Name

English

DAVAINEX

Preferred 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

DESMORAPID Z

Brand Name

English

DODECANOIC ACID 1,1'-(DIBUTYLSTANNYLENE) ESTER

Common Name

English

Classification Tree Code System Code

WHO-VATC

QP52AX04