Triisopropylsilane(TIPS) - ≥98% , CAS No.6485-79-6

CAS: 6485-79-6 Cat. No.: T107280 Formula: C9H22Si Molecular Weight: 158.36 Beilstein Registry Number: 1733718 EC Number: 464-880-1
AVAILABLE TO ORDER
GRADE & PURITY ≥98%
Synonyms
EN300-117959 | J-525100 | tris(propan-2-yl)silane | PD118098 | AKOS006222744 | AS-19155 | Aksci Bulk ReagentTriisopropylsilane | Triisopropylsilane, 98% | A14931 | AKOS030228028 | Benzenesulfonic acid,5-[(4-amino-1-naphthalenyl)azo]-2-[2-[4-[(2-hydroxy-1-
Storage
Room temperature,Argon charged
Shipped In
Normal
★
Size
USA
Germany (EU)*
Price
Qty
5ml
T107280-5ml
In stock ≥10
7 In stock
$9.90
25ml
T107280-25ml
2 In stock
—
$19.90
100ml
T107280-100ml
2 In stock
—
$39.90
500ml
T107280-500ml
2 In stock
—
$125.90
Enter a quantity for the sizes you want to add.

Overview

Triisopropylsilane (TIPS) is an organosilicon compound that is low in toxicity, easy to handle, and capable of selectively reducing various functional groups, making it suitable as a reducing agent in organic synthesis. In the presence of Lewis acids (e.g., titanium tetrachloride), it can selectively reduce ketones and aldehydes to their corresponding alkanes, and epoxides to their corresponding alcohols.

Specifications

Synonyms
EN300-117959 | J-525100 | tris(propan-2-yl)silane | PD118098 | AKOS006222744 | AS-19155 | Aksci Bulk ReagentTriisopropylsilane | Triisopropylsilane, 98% | A14931 | AKOS030228028 | Benzenesulfonic acid,5-[(4-amino-1-naphthalenyl)azo]-2-[2-[4-[(2-hydroxy-1-
Specifications & Purity
≥98%
Application
Triisopropylsilane can be used as a reducing agent: In the synthesis of 4-pyrrolobenzoyl peptides during solid-phase peptide synthesis. In the reaction of amides with hydrosilanes catalyzed by transition metal complexes. For the selective reduction of C-a
Storage
Room temperature,Argon charged
Shipped In
Normal
Purity
≥98%
Names and Identifiers
Pubchem Sid
Pubchem Sid Url
https://pubchem.ncbi.nlm.nih.gov/substance/504764056
Canonical Smiles
CC(C)[Si](C(C)C)C(C)C
InChIKey
ZGYICYBLPGRURT-UHFFFAOYSA-N
INCHI
1S/C9H21Si/c1-7(2)10(8(3)4)9(5)6/h7-9H,1-6H3
Isomeric SMILES
CC(C)[Si](C(C)C)C(C)C
WGK Germany
3
UN Number
1993
Molecular Weight
158.36
Beilstein
1733718
Reaxy-Rn
1733718

Advanced Data

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassHydrocarbon derivatives
ClassNot available
SubclassNot available
Intermediate Tree Nodes Not available
Direct ParentHydrocarbon derivatives
Alternative Parents Organosilicon compounds  
Molecular FrameworkAliphatic acyclic compounds
Substituents Hydrocarbon derivative - Organosilicon compound - Organic metalloid moeity - Aliphatic acyclic compound
DescriptionThis compound belongs to the class of organic compounds known as hydrocarbon derivatives. These are derivatives of hydrocarbons obtained by substituting one or more carbon atoms by an heteroatom. They contain at least one carbon atom and heteroatom.
External Descriptors Not available
3D Structure
Interactive Chemical Structure Model





Certificates (CoA,COO,BSE/TSE and Analysis Chart)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

68 results found

Lot NumberCertificate TypeDateItem
F1928105F1928105Certificate of AnalysisOct 13, 2026 T107280
J2610733J2610733Certificate of AnalysisSep 28, 2026 T107280
J2610732J2610732Certificate of AnalysisSep 28, 2026 T107280
J2610731J2610731Certificate of AnalysisSep 28, 2026 T107280
J2610730J2610730Certificate of AnalysisSep 28, 2026 T107280
A2314313A2314313Certificate of AnalysisJul 06, 2026 T107280
A2314329A2314329Certificate of AnalysisJul 06, 2026 T107280
H2625100H2625100Certificate of AnalysisMar 28, 2026 T107280
D2622508D2622508Certificate of AnalysisMar 28, 2026 T107280
D2622472D2622472Certificate of AnalysisMar 28, 2026 T107280
D2622469D2622469Certificate of AnalysisMar 28, 2026 T107280
D2622458D2622458Certificate of AnalysisMar 28, 2026 T107280
D2416515D2416515Certificate of AnalysisJan 21, 2026 T107280
F2222396F2222396Certificate of AnalysisDec 10, 2025 T107280
F2222397F2222397Certificate of AnalysisDec 10, 2025 T107280
L2501549L2501549Certificate of AnalysisNov 21, 2025 T107280
L2501548L2501548Certificate of AnalysisNov 21, 2025 T107280
L2501542L2501542Certificate of AnalysisNov 21, 2025 T107280
K2224641K2224641Certificate of AnalysisNov 13, 2025 T107280
K2224644K2224644Certificate of AnalysisNov 13, 2025 T107280
K2224645K2224645Certificate of AnalysisNov 13, 2025 T107280
K2224646K2224646Certificate of AnalysisNov 13, 2025 T107280
A2411444A2411444Certificate of AnalysisOct 13, 2025 T107280
A2411445A2411445Certificate of AnalysisOct 13, 2025 T107280
K21111076K21111076Certificate of AnalysisMay 09, 2025 T107280
K21111038K21111038Certificate of AnalysisMay 09, 2025 T107280
B2506644B2506644Certificate of AnalysisJan 20, 2025 T107280
B2506682B2506682Certificate of AnalysisJan 20, 2025 T107280
B2506681B2506681Certificate of AnalysisJan 20, 2025 T107280
B2506645B2506645Certificate of AnalysisJan 20, 2025 T107280
A2514093A2514093Certificate of AnalysisJan 07, 2025 T107280
A2514092A2514092Certificate of AnalysisJan 07, 2025 T107280
H2413500H2413500Certificate of AnalysisJun 28, 2024 T107280
H2413498H2413498Certificate of AnalysisJun 28, 2024 T107280
H2413494H2413494Certificate of AnalysisJun 28, 2024 T107280
D2416517D2416517Certificate of AnalysisMar 12, 2024 T107280
D2416516D2416516Certificate of AnalysisMar 12, 2024 T107280
C2429736C2429736Certificate of AnalysisMar 12, 2024 T107280
C2429727C2429727Certificate of AnalysisMar 12, 2024 T107280
C2429726C2429726Certificate of AnalysisMar 12, 2024 T107280
C2429724C2429724Certificate of AnalysisMar 12, 2024 T107280
C2429718C2429718Certificate of AnalysisMar 12, 2024 T107280
C2429734C2429734Certificate of AnalysisMar 12, 2024 T107280
C2429720C2429720Certificate of AnalysisMar 12, 2024 T107280
C2429723C2429723Certificate of AnalysisMar 12, 2024 T107280
C2429733C2429733Certificate of AnalysisMar 12, 2024 T107280
C2429728C2429728Certificate of AnalysisMar 12, 2024 T107280
C2429729C2429729Certificate of AnalysisMar 12, 2024 T107280
C2429719C2429719Certificate of AnalysisMar 12, 2024 T107280
K2320411K2320411Certificate of AnalysisOct 30, 2023 T107280
K2320410K2320410Certificate of AnalysisOct 30, 2023 T107280
K2320404K2320404Certificate of AnalysisOct 30, 2023 T107280
H2328013H2328013Certificate of AnalysisAug 25, 2023 T107280
H2328012H2328012Certificate of AnalysisAug 25, 2023 T107280
K21111077K21111077Certificate of AnalysisAug 03, 2023 T107280
G2329461G2329461Certificate of AnalysisMay 31, 2023 T107280
G2329476G2329476Certificate of AnalysisMay 31, 2023 T107280
G2329480G2329480Certificate of AnalysisMay 31, 2023 T107280
A1808011A1808011Certificate of AnalysisMay 09, 2023 T107280
D2123105D2123105Certificate of AnalysisJan 17, 2023 T107280
D2123103D2123103Certificate of AnalysisJan 17, 2023 T107280
A2314323A2314323Certificate of AnalysisJan 06, 2023 T107280
K2224651K2224651Certificate of AnalysisOct 11, 2022 T107280
K2009264K2009264Certificate of AnalysisAug 15, 2022 T107280
F2222399F2222399Certificate of AnalysisJun 11, 2022 T107280
F2222400F2222400Certificate of AnalysisJun 11, 2022 T107280
K21111039K21111039Certificate of AnalysisOct 25, 2021 T107280
K21111040K21111040Certificate of AnalysisOct 25, 2021 T107280
Chemical and Physical Properties
SolubilityImmiscible with water.
SensitivityMoisture sensitive.
Refractive Index1.434
Flash Point(°F)100.4 °F
Flash Point(°C)38 °C
Boil Point(°C)84-86 °C/35 mmHg (lit.)
Molecular Weight157.350 g/mol
XLogP3
Hydrogen Bond Donor Count0
Hydrogen Bond Acceptor Count0
Rotatable Bond Count3
Exact Mass157.141 Da
Monoisotopic Mass157.141 Da
Topological Polar Surface Area0.000 Ų
Heavy Atom Count10
Formal Charge0
Complexity65.700
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count1
Documents & Articles
A Complete Guide to Choosing Resins for SPPS (Solid-Phase Peptide Synthesis): Fmoc/Boc Routes, C-Terminal Acid/Amide, and a Key-Parameter Navigator
From Analytical Instrument to Synthetic Platform: A New Strategy for Reconstructing Automated Flow Solid-Phase Peptide Synthesis with Standard Analytical HPLC
New Progress in the Solid-Phase Synthesis of Sterically Hindered Peptides: Background, Core Breakthroughs, and Implications for Automation Compatibility of the RMMR Strategy
Low Racemization in Peptide Synthesis Is Not Just About Reagent Choice: Stereochemical Risk During the Activation Stage and Practical Strategies for Experimental Control
Decision Logic for Peptide Synthesis Routes: Applicability and Criteria for Choosing among SPPS, LPPS, and Recombinant Expression
Boc₂O Selection Cannot Be Judged by Protection Installation Alone: Experimental Decision-Making from Substrate Nucleophilicity and Medium Effects to Deprotection Pathways
How to Troubleshoot Abnormal Impurities in Peptide Synthesis? Locating Process Issues Through Amino-Related Side Reactions
Peptide Intermediates Difficult to Dissolve and Separate? Route Design and Workup Strategies for Tag-Assisted Liquid-Phase Peptide Synthesis (TAG-LPPS)
Formation and Control of Carboxyl- and Hydroxyl-Related Impurities in Peptide Synthesis — Using Asp/Glu and Ser/Thr Residue Side Reactions as Examples
Citations of This Product
Solution Calculators
Reviews

Customer Reviews

Shall we send you a message when we have discounts available?

Remind me later

Thank you! Please check your email inbox to confirm.

Oops! Notifications are disabled.