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ChemicalBook Product Catalog Chemical Reagents Organic reagents Silane Triisopropylsilane

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Triisopropylsilane

$ 1.00 /1KG

Min. Order1G
Purity99%
Cas No6485-79-6
Supply Ability100kg
Update time2019-07-06

career henan chemical co

career henan chemical co

7YR

China

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Chemical Properties

Product Name	Triisopropylsilane
CAS No	6485-79-6
EC-No	464-880-1
Min. Order	1G
Purity	99%
Supply Ability	100kg
Release date	2019/07/06

AD68

Triisopropylsilane Basic information

Product Name:	Triisopropylsilane
Synonyms:	Tris-isopropylsilane;(ME2CH)3SIH;SILANE IP3H;TIS;TIPS;TRIISOPROPYLSILANE;Triisopropylsilane (TIPS);Triisopropylsilane [Cas#
CAS:	6485-79-6
MF:	C9H22Si
MW:	158.36
EINECS:	464-880-1
Product Categories:	Other Reagents;Reduction;Si (Classes of Silicon Compounds);Si-H Compounds;Silicon Compounds (for Synthesis);Synthetic Organic Chemistry;Alkyl Silanes;Hydrogensilanes Hydrogensiloxanes;Reducing Agents;Biochemics;Organometallic Reagents;Organosilicon;OthersSynthetic Reagents;Silanes;Chemical Synthesis;Organometallic Reagents;Others;Synthetic Reagents
Mol File:	6485-79-6.mol

Triisopropylsilane Chemical Properties

Boiling point	84-86 °C35 mm Hg(lit.)
density	0.773 g/mL at 25 °C(lit.)
refractive index	n20/D 1.434(lit.)
Fp	99 °F
storage temp.	Store at RT.
Water Solubility	Immiscible with water.
Sensitive	Moisture Sensitive
BRN	1733718
InChIKey	YDJXDYKQMRNUSA-UHFFFAOYSA-N
CAS DataBase Reference	6485-79-6(CAS DataBase Reference)

Safety Information

Hazard Codes	Xi
Risk Statements	10-36/37/38
Safety Statements	26-36-37/39-16
RIDADR	UN 1993 3/PG 3
WGK Germany	3
F	10-21
TSCA	No
HazardClass	3
PackingGroup	III

MSDS Information

Provider	Language
SigmaAldrich	English
ACROS	English
ALFA	English

Triisopropylsilane Usage And Synthesis

Chemical Properties	Clear colorless liquid
Uses	The bulky isopropyl groups (vs. ethyl) allow for more selective reductions, e.g., beta-selective reduction of anomeric C-phenyl ketals, but do not diminish their activity (e.g. in the copper triflate catalyzed reductive etherification of trimethylsilyl ethers).
Uses	Selective silylation of primary hydroxy groups in the presence of secondary alcohol.

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