Determine the necessary mass, volume, or concentration for preparing a solution.
≥97% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
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 1 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Product Introduction
Electrochemical homopolymerization of 3-chlorothiophene and copolymerization with 3-methylthiophene in ionic liquid has been investigated by potentiodynamic and galvanostat methods
Application
3-Chlorothiophene was used in the synthesis of poly(3-chlorothiophene) films by direct oxidation in mixed electrolytes of boron trifluoride diethyl etherate and trifluroacetic acid.
| Pubchem Sid | 488186388 |
|---|---|
| Pubchem Sid Url | https://pubchem.ncbi.nlm.nih.gov/substance/488186388 |
| Sorrisi canonici | C1=CSC=C1Cl |
| IUPAC Name | 3-chlorothiophene |
| InChIKey | QUBJDMPBDURTJT-UHFFFAOYSA-N |
| INCHI | 1S/C4H3ClS/c5-4-1-2-6-3-4/h1-3H |
| Isomeri SMILES | C1=CSC=C1Cl |
| Numero UN | 1993 |
| Peso molecolare | 118.58 |
| Reaxy-Rn | 105255 |
| Reaxys-RN_link_address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=105255&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 | Organohalogen compounds |
| Classe | Aryl halides |
| Subclass | Aryl chlorides |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Aryl chlorides |
| Alternative Parents | Thiophenes Heteroaromatic compounds Organochlorides Hydrocarbon derivatives |
| Molecular Framework | Aromatic heteromonocyclic compounds |
| Substituents | Aryl chloride - Heteroaromatic compound - Thiophene - Organoheterocyclic compound - Hydrocarbon derivative - Organochloride - Aromatic heteromonocyclic compound |
| Descrizione | This compound belongs to the class of organic compounds known as aryl chlorides. These are organic compounds containing the acyl chloride functional group. |
| External Descriptors | Not available |
Find and download the COA for your product by matching the lot number on the packaging.
| Lot Number | Certificate Type | Data | Oggetto |
|---|---|---|---|
| Certificate of Analysis | Sep 04, 2025 | C101614 | |
| Certificate of Analysis | Sep 29, 2024 | C101614 | |
| Certificate of Analysis | Sep 29, 2024 | C101614 | |
| Certificate of Analysis | Sep 29, 2024 | C101614 | |
| Certificate of Analysis | Sep 29, 2024 | C101614 | |
| Certificate of Analysis | Sep 29, 2024 | C101614 | |
| Certificate of Analysis | Sep 29, 2024 | C101614 | |
| Certificate of Analysis | Oct 19, 2023 | C101614 | |
| Certificate of Analysis | Jun 14, 2022 | C101614 | |
| Certificate of Analysis | Mar 04, 2021 | C101614 |
| Sensibilità | light sensitive |
|---|---|
| Indice di rifrazione | 1.553 |
| Punto di infiammabilità (°F) | 98.6 °F |
| Punto di infiammabilità (°C) | 37 °C |
| Punto di ebollizione (°C) | 137-139°C |
| Peso molecolare | 118.590 g/mol |
| XLogP3 | 2.600 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 1 |
| Rotatable Bond Count | 0 |
| Exact Mass | 117.964 Da |
| Monoisotopic Mass | 117.964 Da |
| Topological Polar Surface Area | 28.200 Ų |
| Heavy Atom Count | 6 |
| Formal Charge | 0 |
| Complexity | 46.800 |
| 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. Xufeng Xiao, Kai Chen, Mi Qin, Xiaoyu Li, Ranjun Meng, Xiaoru Wang, Yang Zhou, Anyi Mei, Hongwei Han. (2025) Alkyl chain length engineering of zwitterionic sulfobetaine passivators for efficient printable mesoscopic perovskite solar cells. CHEMICAL ENGINEERING JOURNAL, [PMID:] [10.1016/j.cej.2025.163528] |