Me3SnOH

Base Information

Chemical Name:Me3SnOH
CAS No.:56-24-6
Molecular Formula:C3H10 O Sn
Molecular Weight:180.822
Hs Code.:
Wikidata:Q27251132
Mol file:56-24-6.mol

Synonyms:Me3SnOH;trimethylstannanylium;hydroxide;SCHEMBL206415;OJZNYUDKNVNEMV-UHFFFAOYSA-M;AKOS025293865;Q27251132

Suppliers and Price of Me3SnOH

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

TRC
TrimethyltinHydroxide
500mg
$ 115.00

Strem Chemicals
Trimethyltin hydroxide, 98%
2g
$ 62.00

Strem Chemicals
Trimethyltin hydroxide, 98%
10g
$ 248.00

Strem Chemicals
Trimethyltin hydroxide, 98%
50g
$ 998.00

Medical Isotopes, Inc.
TrimethyltinHydroxide
2.5 g
$ 850.00

American Custom Chemicals Corporation
TRIMETHYLTIN HYDROXIDE 95.00%
25G
$ 1722.11

American Custom Chemicals Corporation
TRIMETHYLTIN HYDROXIDE 95.00%
1G
$ 645.18

American Custom Chemicals Corporation
TRIMETHYLTIN HYDROXIDE 95.00%
5G
$ 943.52

Alfa Aesar
Trimethyltin hydroxide, 98%
25g
$ 759.00

Alfa Aesar
Trimethyltin hydroxide, 98%
5g
$ 191.00

Total 65 raw suppliers

Chemical Property of Me3SnOH

Chemical Property:

Melting Point:118°C
Boiling Point:80°C
PKA:6.36±0.70(Predicted)
Flash Point:°C
PSA：20.23000
Density:g/cm³
LogP:0.81360
Sensitive.:Moisture Sensitive
Water Solubility.:Soluble in water.
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:0
Exact Mass:181.975367
Heavy Atom Count:5
Complexity:8

Purity/Quality:

99%, ^*data from raw suppliers

TrimethyltinHydroxide ^*data from reagent suppliers

Safty Information:

Pictogram(s): A poison. TWA 0.1 mg(Sn)/m³; STEL 0.2 mg(Sn)/m³ (skin).
Hazard Codes: T+:Very toxic;
Statements: 20/21/22
Safety Statements: 22-36/37/39-45

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C[Sn+](C)C.[OH-]
Uses Drug. Trimethyltin hydroxide is used in the synthesis of modified thymines, which is useful as inhibitors of RNase A. It is also used in the preparation of ketoheterocycle inhibitors of fatty acid amide inhibitors. It reacts with 2,2-disubstituted benzothiazolines to form trialkyltin derivatives of sulphur containing Schiff base complexes.

Technology Process of Me3SnOH

There total 43 articles about Me3SnOH which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 85.0%

: 27640-06-8
(CH₃)3SnCH₂C₆H₄-m-Cl

: 56-24-6
trimethyltin(IV) hydroxide

Guidance literature:: With sodium hydroxide; In ethanol; water; byproducts: m-chlorotoluene; refluxing for 52 h;;

Reference yield: 63.0%

: 697-91-6
2,6-dichloro-1,4-benzoquinone

: 661-69-8
hexamethyldistannane

: 76279-09-9
C₆Cl₂H₂(OSn(CH₃)3)2

: 56-24-6
trimethyltin(IV) hydroxide

Guidance literature:: In benzene; keeping at room temp. (N2) for 4 d; various yields in various conditions; evapn.; elem. anal.;

Reference yield: 47.0%

: 7029-29-0
tris(trimethylstannyl)stibine

: 1692-18-8
bis(trimethyltin)oxide

: 68354-51-8
tetrakis(trimethylstannyl)distibane

: 56-24-6
trimethyltin(IV) hydroxide

Guidance literature:: With oxygen; In neat (no solvent); stibane left in air for 3 d; suspending in Ar-satd. acetone, decanting, recrystn. of red residue from toluene (2nd and 3rd product isolated from acetone suspn.); elem. anal.;