Determine the necessary mass, volume, or concentration for preparing a solution.
≥95% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Argon charged,Room temperature Ships Normal Check lot-specific COA for exact specifications.
SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.
Cited in 2 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
| Pubchem Sid | 488183722 |
|---|---|
| Pubchem Sid Url | https://pubchem.ncbi.nlm.nih.gov/substance/488183722 |
| Sonrisas canónicas | CCCC[Si](C)(C)Cl |
| IUPAC Name | butyl-chloro-dimethylsilane |
| InChIKey | MXOSTENCGSDMRE-UHFFFAOYSA-N |
| INCHI | 1S/C6H15ClSi/c1-4-5-6-8(2,3)7/h4-6H2,1-3H3 |
| Isómeros SMILES | CCCC[Si](C)(C)Cl |
| WGK Alemania | 1 |
| Número ONU | 2985 |
| Grupo de embalaje | II |
| Peso molecular | 150.72 |
| Beilstein | 1732570 |
| Reaxy-Rn | 1732573 |
| Reaxys-RN_link_address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1732573&ln= |
Comprehensive hazard, handling, storage, and regulatory compliance document.
Download SDS →Lot-specific quality data. Enter your lot number to retrieve the exact COA.
Look up COA →Full quality attributes and acceptance criteria for this grade.
View spec sheet →Taxonomy Tree
| Kingdom | Organic compounds |
|---|---|
| Superclass | Organometallic compounds |
| Clase | Organometalloid compounds |
| Subclass | Organosilicon compounds |
| Intermediate Tree Nodes | Organoheterosilanes - Trialkylheterosilanes |
| Direct Parent | Trialkylchlorosilanes |
| Alternative Parents | Silyl monohalides Organochlorosilanes Organic metalloid salts Alkylhalosilanes Hydrocarbon derivatives |
| Molecular Framework | Aliphatic acyclic compounds |
| Substituents | Trialkylchlorosilane - Silyl monohalide - Organochlorosilane - Organic metalloid salt - Alkylhalosilane - Hydrocarbon derivative - Organic salt - Aliphatic acyclic compound |
| Descripción | This compound belongs to the class of organic compounds known as trialkylchlorosilanes. These are organoheterosilanes, bearing a silicon atom linked to three alkyl groups and one chlorine atom. |
| External Descriptors | Not available |
Find and download the COA for your product by matching the lot number on the packaging.
| Lot Number | Certificate Type | Fecha | Articulo |
|---|---|---|---|
| Certificate of Analysis | Mar 23, 2023 | B572936 | |
| Certificate of Analysis | Mar 23, 2023 | B572936 | |
| Certificate of Analysis | Mar 23, 2023 | B572936 | |
| Certificate of Analysis | Mar 23, 2023 | B572936 | |
| Certificate of Analysis | Mar 23, 2023 | B572936 | |
| Certificate of Analysis | Mar 23, 2023 | B572936 | |
| Certificate of Analysis | Mar 23, 2023 | B572936 |
| Sensibilidad | Sensitive to humidity |
|---|---|
| Índice de refracción | 1.42 |
| Punto de inflamación (°F) | 64.4 °F |
| Punto de inflamación (°C) | 27°C(lit.) |
| Punto de ebullición (°C) | 138°C(lit.) |
| Peso molecular | 150.720 g/mol |
| XLogP3 | |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 0 |
| Rotatable Bond Count | 3 |
| Exact Mass | 150.063 Da |
| Monoisotopic Mass | 150.063 Da |
| Topological Polar Surface Area | 0.000 Ų |
| Heavy Atom Count | 8 |
| Formal Charge | 0 |
| Complexity | 61.500 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| The total count of all stereochemical bonds | 0 |
| Covalently-Bonded Unit Count | 1 |
| 1. Soumia Cheddah, Zihang Xia, Yan Wang, Chao Yan. (2023) Effect of Hydrophobic Moieties on the Assembly of Silica Particles into Colloidal Crystals. LANGMUIR, [PMID:37021773] [10.1021/acs.langmuir.2c03155] |
| 2. Wanbin Zhang, Guanghua Zhang, Lun Du, Ce Zhang, Lu Li, Junfeng Zhu, Jing Pei, Jiang Wu. (2018) Synthesis of hydroxyl-terminated polybutadiene bearing pendant carboxyl groups by combination of anionic polymerization and blue light photocatalytic thiol-ene reaction and its pH-triggered self-assemble behavior. REACTIVE & FUNCTIONAL POLYMERS, [PMID:] [10.1016/j.reactfunctpolym.2018.04.003] |