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2897-46-3

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2897-46-3 Usage

Safety Profile

Poison by skin contact andintravenous routes. Moderately toxic by ingestion. When heated to decomposition itemits acrid smoke and Sn+ fumes.

Check Digit Verification of cas no

The CAS Registry Mumber 2897-46-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,8,9 and 7 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 2897-46:
(6*2)+(5*8)+(4*9)+(3*7)+(2*4)+(1*6)=123
123 % 10 = 3
So 2897-46-3 is a valid CAS Registry Number.
InChI:InChI=1/3C6H13.C2H3O2.Sn/c3*1-3-5-6-4-2;1-2(3)4;/h3*1,3-6H2,2H3;1H2,(H,3,4);/rC20H42O2Sn/c1-4-7-10-13-16-23(19-20(21)22,17-14-11-8-5-2)18-15-12-9-6-3/h4-19H2,1-3H3,(H,21,22)

2897-46-3SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-trihexylstannylacetic acid

1.2 Other means of identification

Product number -
Other names Stannane,acetoxytrihexyl

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:2897-46-3 SDS

2897-46-3Upstream product

2897-46-3Downstream Products

2897-46-3Relevant articles and documents

RECYCLING OF ORGANOTIN COMPOUNDS

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Page/Page column 29; 36, (2013/12/03)

A method for the synthesis of a first organic molecule, said method comprising the steps of: a) Reacting a first reactant with an organotin reactant having at least one optionally substituted organic group having from 5 to 20 carbon atoms selected from alkyl, alkenyl, alkynyl, alkoxyalkyl, alkoxy, alkylthioalkyl, carboxylates and alkylaminoalkyl groups, thereby forming a mixture of a product and a tin-containing by-product, and b) Removing most of the tin-containing by-product from said mixture in such a way as to provide a purified product comprising less than 1000 ppm of remaining tin-containing by- product, wherein said step of removing most of said tin-containing by-product is either an extraction between a first liquid and a second liquid, said second liquid being more polar than said first liquid and at least partly immiscible therewith or is a reversed phase chromatography.

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