Skip to Content
Merck
All Photos(1)

Key Documents

View All Documentation

337005

Sigma-Aldrich

1,3-Dichloro-1,1,3,3-tetraisopropyldisiloxane

97%

Synonym(s):

TIPDSiCl2

Sign Into View Organizational & Contract Pricing
All Photos(1)

About This Item

Linear Formula:
[(CH3)2CH]2Si(Cl)OSi(Cl)[CH(CH3)2]2
CAS Number:
69304-37-6
Molecular Weight:
315.43
Beilstein:
1934216
MDL number:
MFCD00009655
UNSPSC Code:
12352001
PubChem Substance ID:
24860447
NACRES:
NA.22

Assay

97%

form

liquid

refractive index

n20/D 1.454 (lit.)

bp

70 °C/0.5 mmHg (lit.)

density

0.986 g/mL at 25 °C (lit.)

SMILES string

CC(C)[Si](Cl)(O[Si](Cl)(C(C)C)C(C)C)C(C)C

InChI

1S/C12H28Cl2OSi2/c1-9(2)16(13,10(3)4)15-17(14,11(5)6)12(7)8/h9-12H,1-8H3

InChI key

DDYAZDRFUVZBMM-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

Pictograms

Corrosion
GHS05

Signal Word

Danger

Hazard Statements

H290,H314

Hazard Classifications

Eye Dam. 1 - Met. Corr. 1 - Skin Corr. 1B

Storage Class Code

8A - Combustible corrosive hazardous materials

WGK

WGK 3

Flash Point(F)

168.8 °F

Flash Point(C)

76 °C

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

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

Visit the Document Library

The Journal of Organic Chemistry, 58, 2552-2552 (1993)
W T Markiewicz et al.
Nucleic acids symposium series, (7)(7), 115-127 (1980-01-01)
Recent results concerning the synthesis of oligoribonucleotides via the phosphotriester method, such as functionalization of ribonucleosides, new phosphorylating agents, 5'-O-sulfonylation and chromatography on Sephadex LH-20 for monitoring the removal of internucleotide phosphotriester groups, are presented. To show that efficiency of
Aldrichimica Acta, 15, 11-11 (1982)
M Kwiatkowski et al.
Nucleic acids research, 24(23), 4632-4638 (1996-12-01)
The synthesis of oligodeoxynucleotides is marred by several problems that contribute to the formation of defective molecules. This in turn seriously limits the usefulness of such reagents in DNA diagnostics, molecular cloning, DNA structural analysis and in antisense therapy. In
Suetying Chow et al.
Nucleosides, nucleotides & nucleic acids, 22(5-8), 583-587 (2003-10-21)
An improved strategy for the synthesis of 2'-O-methyl-guanosine (6) and 2'-MOE-guanosine (8) is reported. The regioselectivity of the alkylation was attained using a novel silicon-based protecting group, methylene-bis (diisopropyl-silylchloride) (MDPSCl2, 2). The alkylation proceeded in a chemoselective manner using NaHMDS

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