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8.41359

Sigma-Aldrich

Triisopropylsilane

for synthesis

Synonym(s):

Triisopropylsilane

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About This Item

Linear Formula:
((CH3)2CH)3SiH
CAS Number:
Molecular Weight:
158.36
MDL number:
UNSPSC Code:
12352103
NACRES:
NA.22

Quality Level

Assay

≥98.0% (GC)

form

liquid

bp

84-85 °C/46.7 hPa

transition temp

flash point 35 °C

density

0.77 g/cm3 at 20 °C

storage temp.

2-30°C

InChI

1S/C9H22Si/c1-7(2)10(8(3)4)9(5)6/h7-10H,1-6H3

InChI key

YDJXDYKQMRNUSA-UHFFFAOYSA-N

Application

  • Total synthesis of diazaquinomycins H and J using double Knorr cyclization: This paper covers the first total synthesis of diazaquinomycins, highlighting the role of triisopropylsilane in enhancing reaction efficiency (Prior & Sun, 2019).
  • Reduction of cysteine‐S‐protecting groups by triisopropylsilane: An in-depth look at the chemical properties of triisopropylsilane, emphasizing its effectiveness in peptide synthesis processes (Ste. Marie & Hondal, 2018).

Analysis Note

Assay (GC, area%): ≥ 98.0 % (a/a)
Density (d 20 °C/ 4 °C): 0.765 - 0.772
Identity (IR): passes test

Pictograms

Flame

Signal Word

Warning

Hazard Statements

Hazard Classifications

Flam. Liq. 3

Storage Class Code

3 - Flammable liquids

WGK

WGK 3

Flash Point(F)

100.4 °F - closed cup

Flash Point(C)

38 °C - closed cup


Certificates of Analysis (COA)

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Protocols

Fmoc resin cleavage and deprotection are crucial steps for peptide synthesis, yielding the desired peptide after resin detachment.

Fmoc resin cleavage and deprotection are crucial steps for peptide synthesis, yielding the desired peptide after resin detachment.

Fmoc resin cleavage and deprotection are crucial steps for peptide synthesis, yielding the desired peptide after resin detachment.

Fmoc resin cleavage and deprotection are crucial steps for peptide synthesis, yielding the desired peptide after resin detachment.

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