Triphenylsilane - ≥96%(GC) , CAS No.789-25-3

CAS: 789-25-3 Cat. No.: T162508 Molecular Weight: 260.41 Beilstein Registry Number: 978182 EC Number: 212-333-0 PubChem CID: 6327682
AVAILABLE TO ORDER
GRADE & PURITY ≥96%(GC)
Synonyms
NSC 12565 | 1,1',1''-Silylidynetrisbenzene | UNII-UQL9QY2CS8 | Benzene, 1,1',1''-silylidynetris- | J-525126 | EN300-7425612 | T0661 | triphenylhydrosilane | triphenylsilicon;Triphenylsilane | S20600 | DTXSID10883583 | FT-0632957 | triphenylsilicon | AS-14
Storage
Argon charged,Room temperature
Shipped In
Normal
 ·  off list, applied to all prices below.
Size
Status
Price
Qty
1g
T162508-1g
3
$9.90
5g
T162508-5g
3
$10.90
10g
T162508-10g
2

$11.90

$17.90
Save $6.00 (33.52%)
25g
T162508-25g
2

$28.90

$43.90
Save $15.00 (34.17%)
50g
T162508-50g
1

$52.90

$79.90
Save $27.00 (33.79%)
100g
T162508-100g
1

$103.90

$155.90
Save $52.00 (33.35%)
500g
T162508-500g
1

$509.90

$764.90
Save $255.00 (33.34%)
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Why this grade

≥96%(GC) for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Argon charged,Room temperature Ships Normal Check lot-specific COA for exact specifications.

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Quality documents

SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.

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Literature proof

Cited in 4 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Overview

Reactant or reagent: . For catalytic hydrogen deuterium exchange reactions of silanes . To be oxidized by carbon nanotube-gold nanohybrids . For hydrolysis by ruthenium complexes . For hydrosilylation to produce enolsilanes . For synthesis of bromosilanes . For ozone oxidation of silyl-alkenes for synthesis of α-O-silylated acyloin derivatives . Used to synthesize hydrido silyl and bis(silyl) bis(imidazolinylidene) nickel complexes

Specifications

Synonyms
NSC 12565 | 1, 1', 1''-Silylidynetrisbenzene | UNII-UQL9QY2CS8 | Benzene, 1, 1', 1''-silylidynetris- | J-525126 | EN300-7425612 | T0661 | triphenylhydrosilane | triphenylsilicon;Triphenylsilane | S20600 | DTXSID10883583 | FT-0632957 | triphenylsilicon | AS-14
Specifications & Purity
≥96%(GC)
Storage
Argon charged, Room temperature
Shipped In
Normal
Purity
≥96%(GC)
Names and Identifiers
Pubchem Sid504764065
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/504764065
Canonical SmilesC1=CC=C(C=C1)[Si](C2=CC=CC=C2)C3=CC=CC=C3
InChIKeyBZLZKLMROPIZSR-UHFFFAOYSA-N
INCHI1S/C18H15Si/c1-4-10-16(11-5-1)19(17-12-6-2-7-13-17)18-14-8-3-9-15-18/h1-15H
Isomeric SMILES C1=CC=C(C=C1)[Si](C2=CC=CC=C2)C3=CC=CC=C3
WGK Germany 1
PubChem CID 6327682
Molecular Weight 260.41
Beilstein 978182
Reaxy-Rn 978182

Documentation

📋 Safety Data Sheet (SDS)

Comprehensive hazard, handling, storage, and regulatory compliance document.

Download SDS →

✅ Certificate of Analysis (COA)

Lot-specific quality data. Enter your lot number to retrieve the exact COA.

Look up COA →

📊 Datasheet

Quick-reference summary of product specifications and applications.

View datasheet →

🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

View spec sheet →

Advanced Data

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassBenzenoids
ClassBenzene and substituted derivatives
SubclassNot available
Intermediate Tree Nodes Not available
Direct ParentBenzene and substituted derivatives
Alternative Parents Organosilicon compounds  Hydrocarbon derivatives  
Molecular FrameworkAromatic homomonocyclic compounds
Substituents Monocyclic benzene moiety - Hydrocarbon derivative - Organosilicon compound - Aromatic homomonocyclic compound
DescriptionThis compound belongs to the class of organic compounds known as benzene and substituted derivatives. These are aromatic compounds containing one monocyclic ring system consisting of benzene.
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.

17 results found

Lot NumberCertificate TypeDateItem
H2218046Certificate of AnalysisJun 08, 2026 T162508
L2109684Certificate of AnalysisSep 09, 2025 T162508
A1812016Certificate of AnalysisAug 15, 2025 T162508
G2127269Certificate of AnalysisMay 13, 2025 T162508
G2127267Certificate of AnalysisMay 09, 2025 T162508
G2127268Certificate of AnalysisMay 09, 2025 T162508
G2127271Certificate of AnalysisMay 09, 2025 T162508
G2127272Certificate of AnalysisMay 09, 2025 T162508
F2418170Certificate of AnalysisMay 23, 2024 T162508
F2418171Certificate of AnalysisMay 23, 2024 T162508
F2418169Certificate of AnalysisMay 23, 2024 T162508
F2418168Certificate of AnalysisMay 23, 2024 T162508
E2621792Certificate of AnalysisMay 23, 2024 T162508
J2212008Certificate of AnalysisAug 20, 2022 T162508
J2212009Certificate of AnalysisAug 20, 2022 T162508
J2212010Certificate of AnalysisAug 20, 2022 T162508
J2212011Certificate of AnalysisAug 20, 2022 T162508

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Chemical and Physical Properties
SolubilitySoluble in methanol. Decomposes in water
SensitivityMoisture sensitive;Air sensitive
Flash Point(°F)168.8 °F
Flash Point(°C)76 °C
Boil Point(°C)152 °C/2 mmHg
Melt Point(°C)43-45 °C
Molecular Weight259.399 g/mol
XLogP3
Hydrogen Bond Donor Count0
Hydrogen Bond Acceptor Count0
Rotatable Bond Count3
Exact Mass259.094 Da
Monoisotopic Mass259.094 Da
Topological Polar Surface Area0.000 Ų
Heavy Atom Count19
Formal Charge0
Complexity202.000
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
Citations of This Product
References
1. Xue-Li Liu, Yi-Fan Chen, Yi-Wen Chen, Wei-Kang Peng, Han-Chun Liu.  (2022)  Preparation of carbosilane quaternary ammonium surfactants and surface activity.  TENSIDE SURFACTANTS DETERGENTS,  59  (5): (424-432).  [PMID:] [10.1515/tsd-2022-2428]
2. Jun Zhang, Kaijun Dong, Weimin Luo.  (2019)  PdCl2-catalyzed hydrodeoxygenation of 5-hydroxymethylfurfural into 2,5-dimethylfuran at room-temperature using polymethylhydrosiloxane as the hydrogen donor.  CHEMICAL ENGINEERING SCIENCE,      [PMID:] [10.1016/j.ces.2019.03.011]
3. Jing Neng, Chen Xiang, Kan Jia, Xiaohua Nie, Peilong Sun.  (2019)  Morphology-Controlled Versatile One-Pot Synthesis of Hydrophobic Gold Nanodots, Nanobars, Nanorods, and Nanowires and Their Applications in Surface-Enhanced Raman Spectroscopy.  Applied Sciences-Basel,  (5): (935).  [PMID:] [10.3390/app9050935]
4. Li Jingpeng, Zhang Meiyu, Li Wenxuan, Li Zhongshu, Zhu Tingshun, Yang Zhenyu.  (2025)  Direct dehydrocoupling facilitates efficient thiophene anchoring on silicon surfaces.  Nature Communications,  16  (1): (1-10).  [PMID:40683880] [10.1038/s41467-025-62002-7]
Solution Calculators
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