Skip to Content
Merck
CN

289094

tert-Butyldimethylsilanol

99%

Synonym(s):

1-(1,1-Dimethylethyl)-1,1-dimethylsilanol, tert-Butyl(hydroxy)dimethylsilane, tert-Butyldimethylsilanol, tert-Butyldimethylsilyl hydroxide, Dimethyl-tert-butylsilanol

Sign In to View Organizational & Contract Pricing

Select a Size

About This Item

Linear Formula:
(CH3)3CSi(CH3)2OH
CAS Number:
18173-64-3
Molecular Weight:
132.28
Beilstein:
1732777
MDL number:
MFCD00010673
UNSPSC Code:
12352103
PubChem Substance ID:
24857384
NACRES:
NA.22

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

Quality Level

200

Assay

99%

form

liquid

refractive index

n20/D 1.424 (lit.)

bp

139 °C/739 mmHg (lit.)

density

0.84 g/mL at 25 °C (lit.)

SMILES string

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

InChI

1S/C6H16OSi/c1-6(2,3)8(4,5)7/h7H,1-5H3

InChI key

FGWRMMTYIZKYMA-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

Related Categories

Application

tert-Butyldimethylsilanol can be used as a silylating agent for the protection of hydroxyl groups via silylation. It is used:
  • For the preparation of α-chiral ether derivatives by catalytic asymmetric allylic substitution.
  • As an initiator for the polymerization of 1,2 benzenedicarboxaldehyde.
  • In the synthesis of enol silyl ethers.

Pictograms

FlameExclamation mark
GHS02,GHS07

Signal Word

Warning

Hazard Statements

H226,H315,H319,H335

Hazard Classifications

Eye Irrit. 2 - Flam. Liq. 3 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

3 - Flammable liquids

WGK

WGK 3

Flash Point(F)

113.0 °F - closed cup

Flash Point(C)

45 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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
MKCW9345
MKCN9160
MKCC0115
MKBT5217V
MKBK9197V

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

Direct, Iridium-Catalyzed Enantioselective and Regioselective Allylic Etherification with Aliphatic Alcohols
Ueno S and Hartwig J
Angewandte Chemie (International ed. in English), 47(10), 1928-1931 (2008)
Enol Silyl Ethers via Copper (II)-Catalyzed C-O Bond Formation
Chan DG, et al.
Organic Letters, 13(10), 2778-2781 (2011)
Reproducible and scalable synthesis of end-cap-functionalized depolymerizable poly (phthalaldehydes)
DiLauro AM, et al.
Macromolecules, 46(8), 2963-2968 (2013)
Synthesis of hydrolytically stable porphyrin C-and S-glycoconjugates in high yields
Pasetto P, et al.
Chemical Communications (Cambridge, England), 81-82 (2001)
Wei Hong et al.
International journal of nanomedicine, 13, 6297-6309 (2018-10-24)
Multidrug-resistant (MDR) Streptococcus pneumonia constitute a major worldwide public health concern. In our preliminary study, PEGylated nano-self-assemblies of bacitracin A (PEGylated Nano-BA12K) showed strong antibacterial potency against reference S. pneumonia strain (ATCC 49619). In this study, the possibility of applying
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