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Tributyltin hydride - contains 0.05% BHT as stabilizer,97%, high purity , CAS No.688-73-3

5 Citations

COA

Grade & Purity:

≥97%
stabilized with 0.05% BHT

Cas Number: 688-73-3
Molecular Weight: 291.06
Beilstein Registry Number: 3587329
EC Number: 211-704-4
MDL number: MFCD00009416
PubChem CID: 3032732

In stock

Item Number

T106234

Grouped product items
SKU	Size	Availability	Price
T106234-10g	10g	Available within 4-8 weeks(?) Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!	$36.90
T106234-50g	50g	Available within 4-8 weeks(?) Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!	$139.90
T106234-250g	250g	1	$537.90
T106234-500g	500g	1	$826.90

View related series

Organotin Reagents (1) Reducing Agents (16)

Basic Description

Synonyms	T1473 \| A836269 \| DTXSID0040709 \| MFCD00009416 \| Tributlytin \| Tributyltin \| tributyl-tin \| PIILXFBHQILWPS-UHFFFAOYSA-N \| TRIBUTYLTIN HYDRIDE [MI] \| AKOS032949789 \| FT-0636016 \| TBY \| TRIBUTYL TIN \| EINECS 211-704-4 \| GS-6317 \| UNII-4XDX163P3D \| AKOS01590
Specifications & Purity	≥97%, stabilized with 0.05% BHT
Storage Temp	Store at 2-8°C,Argon charged
Shipped In	Wet ice This product requires cold chain shipping. Ground and other economy services are not available.
Product Description	A widely used radical reagent used in reductive cleavage, radical dehalogenation, and intramolecular radical cyclization. Radical promoted intramolecular cyclization leading to isoxazolo-benzaulene ring system. Vinyl tin fragment used in a synthesis of (+)-panepophenanthrin via biomimetic Diels-Alder dimerization. application： Tri-n-butyltin hydride is used as a radical reagent in reductive cleavage, radical dehalogenation and intramolecular radical cyclization. It also promotes intramolecular cyclization leading to isoxazolo-benzaulene ring system. Further, it acts as a reducing agent for the conversion of alkyl halides to hydrocarbons. In addition to this, it is used in a veterinary anthelmintic for poultry and an intermediate to make other butyltin compounds.

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
- Superclass Organometallic compounds
  - Class Organo-post-transition metal compounds
    - Subclass Organotin compounds
      - Level5 Triorganotin compounds
        Level6 Trialkyltins

Kingdom	Organic compounds
Superclass	Organometallic compounds
Class	Organo-post-transition metal compounds
Subclass	Organotin compounds
Intermediate Tree Nodes	Triorganotin compounds
Direct Parent	Trialkyltins
Alternative Parents	Organic salts Hydrocarbon derivatives
Molecular Framework	Aliphatic acyclic compounds
Substituents	Trialkyltin - Hydrocarbon derivative - Organic salt - Aliphatic acyclic compound
Description	This compound belongs to the class of organic compounds known as trialkyltins. These are triorganotin compounds where the tin atom is linked to exactly three alkyl groups.
External Descriptors	Not available
1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61. DOI: 10.1186/s13321-016-0174-y

Names and Identifiers

INCHI	InChI=1S/3C4H9.Sn/c31-3-4-2;/h31,3-4H2,2H3;
InChIKey	PIILXFBHQILWPS-UHFFFAOYSA-N
Smiles	CCCC[Sn](CCCC)CCCC
Isomeric SMILES	CCCC[Sn](CCCC)CCCC
WGK Germany	3
PubChem CID	3032732
UN Number	2788
Packing Group	III
Molecular Weight	291.06
Beilstein	3587329

Certificates（CoA,COO,BSE/TSE and Analysis Chart)

C of A & Other Certificates(BSE/TSE, COO):

Analytical Chart:

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26 results found

Lot Number	Certificate Type	Date	Item
I2321322	Certificate of Analysis	Jun 11, 2025	T106234
D2516078	Certificate of Analysis	Jun 21, 2024	T106234
B2514026	Certificate of Analysis	Jun 21, 2024	T106234
J2417792	Certificate of Analysis	Jun 21, 2024	T106234
J2417796	Certificate of Analysis	Jun 21, 2024	T106234
J2417809	Certificate of Analysis	Jun 21, 2024	T106234
J2417817	Certificate of Analysis	Jun 21, 2024	T106234
C2407158	Certificate of Analysis	Feb 22, 2024	T106234
C2407160	Certificate of Analysis	Feb 22, 2024	T106234
F2523044	Certificate of Analysis	Feb 22, 2024	T106234
C2407159	Certificate of Analysis	Feb 22, 2024	T106234
C2407157	Certificate of Analysis	Feb 22, 2024	T106234
A2203108	Certificate of Analysis	Oct 10, 2023	T106234
I2321323	Certificate of Analysis	Aug 31, 2023	T106234
I2321329	Certificate of Analysis	Aug 31, 2023	T106234
C23021245	Certificate of Analysis	Feb 17, 2023	T106234
C23021239	Certificate of Analysis	Feb 17, 2023	T106234
C2303013	Certificate of Analysis	Feb 17, 2023	T106234
H2209730	Certificate of Analysis	Jul 27, 2022	T106234
H2209727	Certificate of Analysis	Jul 27, 2022	T106234
H2209728	Certificate of Analysis	Jul 27, 2022	T106234
H2209729	Certificate of Analysis	Jul 27, 2022	T106234
F2125244	Certificate of Analysis	Jun 29, 2021	T106234
F2125246	Certificate of Analysis	Jun 29, 2021	T106234
F2125245	Certificate of Analysis	Jun 29, 2021	T106234
F2125251	Certificate of Analysis	Jun 29, 2021	T106234

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Chemical and Physical Properties

Solubility	Immiscible with water.
Sensitivity	Air, Moisture and Heat Sensitive
Refractive Index	1.473
Flash Point(°F)	104 °F
Flash Point(°C)	40℃
Boil Point(°C)	80°C
Melt Point(°C)	0-1℃
Molecular Weight	290.050 g/mol
XLogP3
Hydrogen Bond Donor Count	0
Hydrogen Bond Acceptor Count	0
Rotatable Bond Count	9
Exact Mass	291.113 Da
Monoisotopic Mass	291.113 Da
Topological Polar Surface Area	0.000 Å²
Heavy Atom Count	13
Formal Charge	0
Complexity	72.100
Isotope Atom Count	0
Defined Atom Stereocenter Count	0
Undefined Atom Stereocenter Count	0
Defined Bond Stereocenter Count	0
Undefined Bond Stereocenter Count	0
The total count of all stereochemical bonds	0
Covalently-Bonded Unit Count	1

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