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Distannoxane, 1,3-dibutoxy-1,1,3,3-tetrabutyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 34833-46-0 Structure
  • Basic information

    1. Product Name: Distannoxane, 1,3-dibutoxy-1,1,3,3-tetrabutyl-
    2. Synonyms:
    3. CAS NO:34833-46-0
    4. Molecular Formula: C24H54O3Sn2
    5. Molecular Weight: 628.111
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 34833-46-0.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: Distannoxane, 1,3-dibutoxy-1,1,3,3-tetrabutyl-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Distannoxane, 1,3-dibutoxy-1,1,3,3-tetrabutyl-(34833-46-0)
    11. EPA Substance Registry System: Distannoxane, 1,3-dibutoxy-1,1,3,3-tetrabutyl-(34833-46-0)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 34833-46-0(Hazardous Substances Data)

34833-46-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 34833-46-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,4,8,3 and 3 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 34833-46:
(7*3)+(6*4)+(5*8)+(4*3)+(3*3)+(2*4)+(1*6)=120
120 % 10 = 0
So 34833-46-0 is a valid CAS Registry Number.

34833-46-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name butoxy-[butoxy(dibutyl)stannyl]oxy-dibutylstannane

1.2 Other means of identification

Product number -
Other names 1,1,3,3-tetrabutyl-1,3-dibutoxy-distannoxane

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:34833-46-0 SDS

34833-46-0Relevant articles and documents

PROCESS FOR PRODUCTION OF ALKYL TIN ALKOXIDE COMPOUND, AND PROCESS FOR PRODUCTION OF CARBONATE ESTER USING THE COMPOUND

-

Page/Page column 77, (2010/09/17)

The present invention provides a process for producing : a compound represented by XOR2; a dialkyl tin dialkoxide compound having one tin atom, two Sn-R1 bonds and two Sn-OR2 bonds; and/or a tetraalkyl dialkoxy distannoxane compound having one Sn-O-Sn bond, in which each tin atom of the tetraalkyl dialkoxy distannoxane compound has two Sn-R1 bonds and one Sn-OR2 bond, the process comprising reacting in the absence of a catalyst at least one alkyl tin compound selected from the group consisting of i) and ii) below: i) a dialkyl tin compound having one tin atom, two Sn-R1 (wherein R1 represents an alkyl group) bonds, and two Sn-OX bonds (wherein OX is a group in which HOX that is a conjugate acid of OX is a Bronsted acid having a pKa of from 0 to 6.8); and ii) a tetraalkyl distannoxane compound having one Sn-O-Sn bond, in which each tin atom of the tetraalkyl distannoxane compound has two Sn-R1 bonds and one Sn-OX bond (wherein OX is a group in which HOX that is a conjugate acid of OX is a Bronsted acid having a pKa of from 0 to 6.8); and a carbonic acid ester represented by R2OCOOR2 (wherein R2 represents a linear or branched, saturated or unsaturated hydrocarbon group, a hydrocarbon group having a saturated or unsaturated cyclic hydrocarbon substituent, or a Y-CH2- group (wherein Y represents an alkyl polyalkylene group, an aromatic group or a cyclic saturated or unsaturated alkylene ether group)), and/or an alcohol represented by R2OH (wherein R2 is the same as defined above).

METHOD FOR PRODUCING AROMATIC CARBONATE

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Page/Page column 41; 44-45; 48; 57; 60-61; 71; 74; 78; 114, (2010/11/08)

A method for producing an aromatic carbonate, comprising: (1) performing a reaction between an organometal compound and carbon dioxide to obtain a reaction mixture containing a dialkyl carbonate formed by the reaction,(2) separating the dialkyl carbonate from the reaction mixture to obtain a residual liquid,(3) reacting the residual liquid with an alcohol to form at least one organometal compound and form water and removing the water from the organometal compound, and(4) reacting the dialkyl carbonate separated in step (2) with an aromatic hydroxy compound to obtain an aromatic carbonate.

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