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About This Item
Empirical Formula (Hill Notation):
C2H6Cl2Si
CAS Number:
Molecular Weight:
129.06
UNSPSC Code:
26111700
NACRES:
NB.61
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
605287
Form:
liquid
InChI
1S/C2H6Cl2Si/c1-5(2,3)4/h1-2H3
SMILES string
C[Si](C)(Cl)Cl
InChI key
LIKFHECYJZWXFJ-UHFFFAOYSA-N
product line
Selectophore™
form
liquid
concentration
~5% (dimethyldichlorosilane in heptane)
refractive index
n20/D 1.388
Quality Level
General description
Visit our Sensor Applications portal to learn more.
Other Notes
Ready-to-use solution for silanizing micro-electrodes
dimethyldichlorosilane/heptane 1/30 (v/v)
Legal Information
Selectophore is a trademark of Merck KGaA, Darmstadt, Germany
signalword
Danger
hcodes
Hazard Classifications
Aquatic Acute 1 - Aquatic Chronic 1 - Asp. Tox. 1 - Eye Dam. 1 - Flam. Liq. 2 - Skin Corr. 1A - STOT SE 3
target_organs
Central nervous system
Storage Class
3 - Flammable liquids
wgk
WGK 2
flash_point_f
24.8 °F - closed cup
flash_point_c
-4 °C - closed cup
ppe
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
Regulatory Information
危险化学品
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María Jesús Andrés-Costa et al.
Scientific reports, 7(1), 15777-15777 (2017-11-19)
European legislation focusing on water quality is expected to broaden to encompass several pharmaceuticals as priority hazardous substances. This manuscript aims to challenge current regulatory approaches that do not recognize stereochemistry of chiral pharmaceuticals by testing the hypothesis that environmental
Ion-selective electrode for intracellular potassium measurements.
A Haemmerli et al.
Analytical chemistry, 52(8), 1179-1182 (1980-07-01)
Wonmi Ahn et al.
ACS nano, 4(7), 4181-4189 (2010-06-23)
Uniform hexagonal arrays of diverse nanotemplated metal structures were formed via selective electroless gold plating on particle-lithographed dimethyldichlorosilane layers. Surface-associated water at silica bead interstices was shown to correlate with the formation of silane rings with outer ring diameters ranging
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
Takehiro Fukuzaki et al.
Organic letters, 4(17), 2877-2880 (2002-08-17)
[reaction: see text] Studies on the connection between the right and left segments of azadirachtin are described. The Ireland-Claisen rearrangement of Li-enolate of the modeled ester with dichlorodimethylsilane in toluene afforded the desired limonoid framework stereoselectively in good yield.
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