Skip to Content
Merck
CN

80430

Dichlorodimethylsilane

Wacker Chemie AG, ≥99.0% (GC)

Synonym(s):

Silane M2, DMDCS, Dimethyldichlorosilane

Sign In to View Organizational & Contract Pricing.

Select a Size

About This Item

Linear Formula:
(CH3)2SiCl2
CAS Number:
75-78-5
Molecular Weight:
129.06
UNSPSC Code:
12352101
NACRES:
NA.22
PubChem Substance ID:
329768859
EC Number:
200-901-0
Beilstein/REAXYS Number:
605287
MDL number:
MFCD00000491
Assay:
≥99.0% (GC)
Form:
liquid

Key Documents

View All Documentation
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist

InChI key

LIKFHECYJZWXFJ-UHFFFAOYSA-N

InChI

1S/C2H6Cl2Si/c1-5(2,3)4/h1-2H3

SMILES string

C[Si](C)(Cl)Cl

assay

≥99.0% (GC)

form

liquid

manufacturer/tradename

Wacker Chemie AG

Quality Level

100

bp

70 °C (lit.)

mp

−76 °C (lit.)

Looking for similar products? Visit Product Comparison Guide

Related Categories

General description

Dichlorodimethylsilane is an organosilicon compound generally used as a protecting group for diols and carbonyl compounds. It is also used as a starting material for the preparation of silicon-based reagents.

Application

Dichlorodimethylsilane can be used:
  • As a silane coupling agent in the synthesis of silica nanoparticles and in their surface modification studies.
  • To prepare polydimethylsiloxane microemulsions by reacting with sodium dodecylpolyoxyethylene sulfate.
  • To prepare a novel heterasumanene where the benzylic carbon atoms of the sumanene are replaced by heteroatom (S, Si) functionalities

Other Notes

prices for bulk quantities on request

signalword

Danger

Hazard Classifications

Acute Tox. 3 Inhalation - Acute Tox. 4 Oral - Eye Dam. 1 - Flam. Liq. 2 - Skin Corr. 1A - STOT SE 3

target_organs

Respiratory system

Storage Class

3 - Flammable liquids

flash_point_f

33.8 °F - closed cup

flash_point_c

1 °C - closed cup

ppe

Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter

Regulatory Information

危险化学品
This item has

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
BCCJ3001
BCCF3092
103112311
BCBS5869V
BCBK0272V

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Search for a COA

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Zhongyan Lu et al.
American journal of physiology. Regulatory, integrative and comparative physiology, 307(5), R558-R570 (2014-06-13)
Ruminal fermentation products such as short-chain fatty acids (SCFA) and CO2 acutely stimulate urea transport across the ruminal epithelium in vivo, whereas ammonia has inhibitory effects. Uptake and signaling pathways remain obscure. The ruminal expression of SLC14a1 (UT-B) was studied
T G Ruardy et al.
Journal of biomedical materials research, 29(11), 1415-1423 (1995-11-01)
In this study, adhesion and spreading of human skin fibroblasts on gradient surfaces of dichlorodimethylsilane (DDS) coupled to glass was investigated. Gradient surfaces were prepared by the diffusion technique and characterized by the Wilhelmy plate technique and characterized by the
S C Lung et al.
Chemosphere, 41(12), 1865-1871 (2000-11-04)
The effects of coating materials on polychlorinated biphenyl (PCB) adsorption in aqueous solution were assessed in an attempt to minimize PCB sorption loss during sampling processes. A coating material, which enhances PCB adsorption and allows adsorbed PCBs to be readily
Y C Tseng et al.
Biomaterials, 16(13), 963-972 (1995-09-01)
Amphipathic ethylene glycol-butadiene block copolymers (PEG-PB) with different chain lengths of poly(ethylene glycol) (PEG) were synthesized by reacting poly(ethylene glycol methyl ether) (m-PEG, mol. wt = 350, 550, 750, 2000 and 5000) with telechelic polybutadiene (PB). The PEG-PB copolymers formed
R Bos et al.
Microbiology (Reading, England), 142 ( Pt 9), 2355-2361 (1996-09-01)
Co-adhesion between oral microbial pairs (i.e. adhesion of a planktonic microorganism to a sessile organism adhering to a substratum surface) has been described as a highly specific interaction, mediated by stereochemical groups on the interacting microbial cell surfaces, and also
View All Related Papers

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service