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3,3'(DICHLOROSTANNYLENE)BIS(METHYLPROPANOATE), with the molecular formula C16H26Cl2O4Sn, is a white solid organotin compound known for its complex structure and significant role as a stabilizer in the plastics industry. Characterized by a molecular weight of 554.18 g/mol and insolubility in water, 3,3'(DICHLOROSTANNYLENE)BIS(METHYLPROPANOATE) is soluble in organic solvents and is recognized for enhancing the heat stability, weatherability, and mechanical properties of polymers, thereby serving as a valuable additive.

10175-01-6

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10175-01-6 Usage

Uses

Used in Plastics Industry:
3,3'(DICHLOROSTANNYLENE)BIS(METHYLPROPANOATE) is used as a stabilizer for improving the heat stability, weatherability, and mechanical properties of polymers such as PVC and other types of plastics. Its inclusion as an additive ensures that the plastics maintain their integrity and performance under various conditions, thus extending their lifespan and utility.
It is crucial to handle 3,3'(DICHLOROSTANNYLENE)BIS(METHYLPROPANOATE) with care due to the potential toxicity of organotin compounds, which can pose risks to both human health and the environment if not managed properly.

Check Digit Verification of cas no

The CAS Registry Mumber 10175-01-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,1,7 and 5 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 10175-01:
(7*1)+(6*0)+(5*1)+(4*7)+(3*5)+(2*0)+(1*1)=56
56 % 10 = 6
So 10175-01-6 is a valid CAS Registry Number.

10175-01-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,3'(DICHLOROSTANNYLENE)BIS(METHYLPROPANOATE)

1.2 Other means of identification

Product number -
Other names bis(2-methoxycarbonylethyl)tin dichloride

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:10175-01-6 SDS

10175-01-6Downstream Products

10175-01-6Relevant academic research and scientific papers

REDISTRIBUTION REACTIONS OF β-CARBOALKOXYETHYLTIN COMPOUNDS

Burley, Joseph W.,Hutton, Ronald E.

, p. 165 - 176 (1981)

Carboalkoxyethyltin compounds undergo redistribution reactions at faster rates than similar unsubstituted alkyltin compounds.In redistribution reactions between SnCl4 and carboalkoxyethyltin compounds stable intermolecular complexes are formed.Rate enhancement is explained in terms of intra- and intermolecular coordination effects.Where strong intermolecular coordination effects are observed, specific electrophilic cleavage of the carboalkoxyethyl group can occur in preference to alkyl cleavage in mixed carboalkoxyethylalkyltin compounds.The presence of a β-ester function can catalyse both alkyl/chlorine and alkyl/alkyl' exchange reactions.

β-SUBSTITUTED ALKYLTIN HALIDES. III. SYNTHESIS OF TRIALKYLTIN HALIDES AND TETRAALKYLTINS

Burley, Joseph W.,Hutton, Ronald E.,Jolley, Michael R.J.,Groenenboom, Cornelis J.

, p. 189 - 202 (2007/10/02)

(β-Carboalkoxyethyl)tin trihalides and bis(β-carboalkoxyethyl)tin dihalides react with metallic zinc to give mixtures of the corresponding tris(β-carboalkoxyethyl)tin halides and the tetra(β-carboalkoxyethyl)tins.Bis(β-carboalkoxyethyl)tin diacetates react with metallic zinc to give only the corresponding tetra(β-carboalkoxyethyl)tin compounds.The mechanisms of these reactions are discussed.Conversion of the bis(β-carboalkoxyethyl)tin dihalides into the tris(β-carboalkoxyethyl)tin halides is believed to occur by a two-step process, with the tetra(β-carboalkoxyethyl)tin compounds as intermediate products.The 270 MHz NMR spectra of the (β-carbobutoxyethyl)tin compounds are presented.

ALCOHOLYSIS OF (2-METHOXYCARBONYL)ETHYLTIN COMPOUNDS

Cheng, Hong-Shing,Hwang, Tsai-Lih,Liu, Chao-Shiuan

, p. 43 - 52 (2007/10/02)

Under acid or base catalysis, di(2-alkoxycarbonylethyl)tin dichlorides of various R groups, (ROCOCH2CH2)2SnCl2, can be prepared conveniently in high yield by alcoholysis of (CH3OCOCH2CH2)2SnCl2 in various alcohols, ROH (R=C2H5, C4H9, iso-C4H9, C5H11, C6H5

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