Dichlorodiphenylsilane - ≥97%(GC) , CAS No.80-10-4

CAS: 80-10-4 Cat. No.: D140820 Molecular Weight: 253.2 Beilstein Registry Number: 609882 EC Number: 201-251-0
AVAILABLE TO ORDER
GRADE & PURITY ≥97%(GC)
Synonyms
Dichlor-difenylsilan [Czech] | Dichloro(diphenyl)silane | WLN: G-SI-GR&R | DICHLORODIPHENYLSILANE | dichloro-diphenyl-silane | MFCD00000489 | NSC 77110 | D0362 | DTXSID2026494 | InChI=1/C12H10Cl2Si/c13-15(14,11-7-3-1-4-8-11)12-9-5-2-6-10-12/h1-10 | dichlo
Storage
Room temperature,Argon charged
Shipped In
FedEx DG Service
 ·  off list, applied to all prices below.
Size
Status
Price
Qty
25g
D140820-25g
10
$15.90
100g
D140820-100g
2
$54.90
500g
D140820-500g
1
$135.90
Enter a quantity for the sizes you want to add.
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Why this grade

≥97%(GC) for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

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Storage & shipping

Room temperature,Argon charged Ships FedEx DG Service 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 9 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Overview

Product Introduction

Dichlorodiphenylsilane is a silane based surface modifier, and a precursor which can be used in the synthesis of silica based materials. It is used to modify the surface by providing toughness, durability and resistance to shock.


Application

The addition reaction of dichlorodiphenylsilane with diglycidyl ether of bisphenol-S yields poly(silyl ether) with pendant chloromethyl groups.  The coupling reaction between dichloromethylsilane and dichlorodiphenylsilane can form diorganosilane-hydrosilane copolymers at -75oC. Heating the compound with tetrabutoxydianilinocyclophosphazene at temperatures between 100oC-160oC may yield cyclophosphazene oligomers.

Specifications

Synonyms
Dichlor-difenylsilan [Czech] | Dichloro(diphenyl)silane | WLN: G-SI-GR&R | DICHLORODIPHENYLSILANE | dichloro-diphenyl-silane | MFCD00000489 | NSC 77110 | D0362 | DTXSID2026494 | InChI=1/C12H10Cl2Si/c13-15(14, 11-7-3-1-4-8-11)12-9-5-2-6-10-12/h1-10 | dichlo
Specifications & Purity
≥97%(GC)
Storage
Room temperature, Argon charged
Shipped In
FedEx DG Service
This product requires cold chain shipping. Ground and other economy services are not available.
Purity
≥97%(GC)
Names and Identifiers
Pubchem Sid504751141
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/504751141
Canonical SmilesC1=CC=C(C=C1)[Si](C2=CC=CC=C2)(Cl)Cl
IUPAC Namedichloro(diphenyl)silane
InChIKeyOSXYHAQZDCICNX-UHFFFAOYSA-N
INCHI1S/C12H10Cl2Si/c13-15(14,11-7-3-1-4-8-11)12-9-5-2-6-10-12/h1-10H
Isomeric SMILES C1=CC=C(C=C1)[Si](C2=CC=CC=C2)(Cl)Cl
WGK Germany 1
RTECS VV3190000
UN Number 1769
Packing Group II
Molecular Weight 253.2
Beilstein 609882
Reaxy-Rn 609882
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=609882&ln=

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 Organochlorosilanes  Organic metalloid salts  Hydrocarbon derivatives  
Molecular FrameworkAromatic homomonocyclic compounds
Substituents Monocyclic benzene moiety - Organoheterosilane - Organochlorosilane - Organic metalloid salt - Hydrocarbon derivative - Organic salt - 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





Associated Targets(non-human)
Nfe2l2 Nuclear factor erythroid 2-related factor 2 (214 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mechanisms of Action
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.

13 results found

Lot NumberCertificate TypeDateItem
J2115633Certificate of AnalysisJul 10, 2025 D140820
J2115634Certificate of AnalysisJul 10, 2025 D140820
J2416453Certificate of AnalysisJul 08, 2024 D140820
A2605048Certificate of AnalysisJan 07, 2023 D140820
B2313566Certificate of AnalysisJan 07, 2023 D140820
B2313598Certificate of AnalysisJan 07, 2023 D140820
B2313599Certificate of AnalysisJan 07, 2023 D140820
B2313600Certificate of AnalysisJan 07, 2023 D140820
B2512049Certificate of AnalysisJan 07, 2023 D140820
J2416232Certificate of AnalysisJan 07, 2023 D140820
B2215516Certificate of AnalysisDec 22, 2021 D140820
B2215533Certificate of AnalysisDec 22, 2021 D140820
B2215540Certificate of AnalysisDec 22, 2021 D140820

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Chemical and Physical Properties
SolubilitySolubility in water: Decomposes
SensitivityMoisture Sensitive.
Refractive Index1.581
Flash Point(°F)287.6 °F
Flash Point(°C)142 °C
Boil Point(°C)305 °C
Melt Point(°C)-22℃
Molecular Weight253.190 g/mol
XLogP3
Hydrogen Bond Donor Count0
Hydrogen Bond Acceptor Count0
Rotatable Bond Count2
Exact Mass251.993 Da
Monoisotopic Mass251.993 Da
Topological Polar Surface Area0.000 Ų
Heavy Atom Count15
Formal Charge0
Complexity174.000
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. Xiaohan Li, Qiunan Xie, Jieying Lin, Jiateng Huang, Kaili Xie, Jingcheng Liu, Xiaojie Li, Wei Wei.  (2023)  A phosphorus/silicon-containing flame retardant based on eugenol for improving flame retardancy and smoke suppression of epoxy resin.  JOURNAL OF APPLIED POLYMER SCIENCE,  140  (39): (e54474).  [PMID:] [10.1002/app.54474]
2. Siyuan He, Cheng Chi, Chaohua Peng, Birong Zeng, Yongming Chen, Zhongxi Miao, Hui Xu, Weiang Luo, Guorong Chen, Zhenping Fu, Lizong Dai.  (2023)  A Novel P/N/Si-Containing Vanillin-Based Compound for a Flame-Retardant, Tough Yet Strong Epoxy Thermoset.  Polymers,  15  (10): (2384).  [PMID:37242961] [10.3390/polym15102384]
3. Ji-Hao Zuo, Yi-Hang Gu, Chao Wei, Xi Yan, Yan Chen, Wan-Zhong Lang.  (2019)  Janus polyvinylidene fluoride membranes fabricated with thermally induced phase separation and spray-coating technique for the separations of both W/O and O/W emulsions.  JOURNAL OF MEMBRANE SCIENCE,      [PMID:] [10.1016/j.memsci.2019.117475]
4. Peng Yang, Mengyuan Ren, Kongfa Chen, Yu Liang, Qiu-Feng Lü, Teng Zhang.  (2019)  Synthesis of a novel silicon-containing epoxy resin and its effect on flame retardancy, thermal, and mechanical properties of thermosetting resins.  Materials Today Communications,      [PMID:] [10.1016/j.mtcomm.2019.01.014]
5. Manman Jin, Jinkai Wang, Bing Wang, Zhenmei Guo, Zhiguo Lv.  (2018)  Highly effective green oxidation of aldehydes catalysed by recyclable tungsten complex immobilized in organosilanes-modified SBA-15.  MICROPOROUS AND MESOPOROUS MATERIALS,      [PMID:] [10.1016/j.micromeso.2018.10.021]
6. Yong Tang, Xiyu Zhang, Zheng Liu, Xiaoya Liu, Xiaojie Li.  (2025)  A resveratrol-based P/Si-containing hyperbranched flame retardant for simultaneously enhancing fire safety and mechanical properties of epoxy thermosets.  CHEMICAL ENGINEERING JOURNAL,      [PMID:] [10.1016/j.cej.2025.160240]
7. Xueying Shan, Qixin Huang, Yuxuan Diao, Boyou Hou, Jiao Gao, Jinchun Li.  (2025)  A Schiff base-derived macromolecular flame retardant: Imparting excellent flame retardancy, UV shielding, and mechanical properties to epoxy resins.  PROGRESS IN ORGANIC COATINGS,      [PMID:] [10.1016/j.porgcoat.2025.109437]
8. Junbo Zang, Jiahui Qi, Jiaxu Zhang, Hao Liu, Chunhong Zhang, Chengyue Zhang, Runtian Wu, Xiaochao Xu, Lei Shang.  (2026)  High-strength, flame-retardant, dielectric Si-functionalized biomass hybrid crosslinked non-isocyanate polyurethane-epoxy for general-purpose adhesive.  POLYMER DEGRADATION AND STABILITY,      [PMID:] [10.1016/j.polymdegradstab.2026.111997]
9. Zhenyang Yin, Yitong Jiang, Fengyu Meng, Xiaoming Qi, Jiangsheng Chen, Hongbo Dai, Chen Qian, Yaqin Fu.  (2026)  Nacre-Inspired Flame-Retardant Coating with a Brick–Mortar Architecture Based on Bio-Based Chitosan/Gelatin and APP/MMT for Flexible Polyurethane Foam.  ACS Applied Polymer Materials,      [PMID:] [10.1021/acsapm.5c04018]
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