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N-BUTYLDIMETHYLSILANE, an organosilicon compound with the chemical formula C6H16Si, is a colorless, flammable liquid characterized by a faint fruity odor. It serves as a reagent in organic synthesis and acts as a precursor for functionalized silanes, making it a versatile chemical with applications in various fields of material science.

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  • 1001-52-1 Structure
  • Basic information

    1. Product Name: N-BUTYLDIMETHYLSILANE
    2. Synonyms: N-BUTYLDIMETHYLSILANE
    3. CAS NO:1001-52-1
    4. Molecular Formula: C6H16Si
    5. Molecular Weight: 116.28
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1001-52-1.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 101-102°C
    3. Flash Point: -6°C
    4. Appearance: /
    5. Density: 0,71 g/cm3
    6. Vapor Pressure: 57.6mmHg at 25°C
    7. Refractive Index: 1.399525
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: N-BUTYLDIMETHYLSILANE(CAS DataBase Reference)
    11. NIST Chemistry Reference: N-BUTYLDIMETHYLSILANE(1001-52-1)
    12. EPA Substance Registry System: N-BUTYLDIMETHYLSILANE(1001-52-1)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: 11
    3. Safety Statements: 3/7-9-16-33
    4. RIDADR: 1993
    5. WGK Germany:
    6. RTECS:
    7. TSCA: No
    8. HazardClass: N/A
    9. PackingGroup: N/A
    10. Hazardous Substances Data: 1001-52-1(Hazardous Substances Data)

1001-52-1 Usage

Uses

Used in Organic Synthesis:
N-BUTYLDIMETHYLSILANE is used as a reagent for introducing a trimethylsilyl group to various functional groups in organic compounds. This silylating agent helps protect sensitive groups, enhancing their stability during subsequent chemical reactions.
Used in the Production of Silicone Oils and Rubbers:
N-BUTYLDIMETHYLSILANE is used as a precursor in the synthesis of silicone oils and rubbers, contributing to the development of materials with unique properties such as heat resistance, flexibility, and biocompatibility.
Used in Metal-Organic Chemical Vapor Deposition (MOCVD) Processes:
In the semiconductor industry, N-BUTYLDIMETHYLSILANE is utilized in MOCVD processes for the production of thin films. This application is crucial for fabricating electronic devices and components with precise control over material properties and layer thicknesses.

Check Digit Verification of cas no

The CAS Registry Mumber 1001-52-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,0,0 and 1 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1001-52:
(6*1)+(5*0)+(4*0)+(3*1)+(2*5)+(1*2)=21
21 % 10 = 1
So 1001-52-1 is a valid CAS Registry Number.
InChI:InChI=1/C6H16Si/c1-4-5-6-7(2)3/h7H,4-6H2,1-3H3

1001-52-1SDS

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 butyl(dimethyl)silane

1.2 Other means of identification

Product number -
Other names Silane,butyldimethyl

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:1001-52-1 SDS

1001-52-1Relevant articles and documents

Molecular Zinc Hydride Cations [ZnH]+: Synthesis, Structure, and CO2 Hydrosilylation Catalysis

Douair, Iskander,Maron, Laurent,Okuda, Jun,Ritter, Florian,Spaniol, Thomas P.

, (2020)

Protonolysis of [ZnH2]n with the conjugated Br?nsted acid of the bidentate diamine TMEDA (N,N,N′,N′-tetramethylethane-1,2-diamine) and TEEDA (N,N,N′,N′-tetraethylethane-1,2-diamine) gave the zinc hydride cation [(L2)ZnH]s

Cleavage of Si-C and Ge-C bonds in heterylsilanes and -germanes by organolithium reagents

Gevorgyan, Vladimir,Borisova, Larisa,Lukevics, Edmunds

, p. 381 - 387 (2007/10/02)

Organolithium reagents RLi can cleave Si-C and Ge-C bonds in heterylsilanes and -germanes substituting furyl, dihydrofuryl and dihydropyranyl groups for the organolithium residue R.

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