Determine the necessary mass, volume, or concentration for preparing a solution.
≥97%(HPLC) for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Room temperature,Argon charged,Desiccated 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 4 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
| Pubchem Sid | 504767687 |
|---|---|
| Pubchem Sid Url | https://pubchem.ncbi.nlm.nih.gov/substance/504767687 |
| Canonical Smiles | C1=C(C(=CC(=C1S)N)S)N.Cl.Cl |
| IUPAC Name | 2,5-diaminobenzene-1,4-dithiol;dihydrochloride |
| InChIKey | HVXLKRWRWNFGBA-UHFFFAOYSA-N |
| INCHI | 1S/C6H8N2S2.2ClH/c7-3-1-5(9)4(8)2-6(3)10;;/h1-2,9-10H,7-8H2;2*1H |
| Isomeric SMILES | C1=C(C(=CC(=C1S)N)S)N.Cl.Cl |
| PubChem CID | 14618269 |
| Molecular Weight | 245.18 |
| Reaxy-Rn | 9431783 |
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 | Benzenoids |
| Class | Thiophenols |
| Subclass | Not available |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Thiophenols |
| Alternative Parents | Aniline and substituted anilines Thiols Primary amines Hydrochlorides Hydrocarbon derivatives |
| Molecular Framework | Aromatic homomonocyclic compounds |
| Substituents | Aniline or substituted anilines - Thiophenol - Monocyclic benzene moiety - Arylthiol - Organic nitrogen compound - Hydrocarbon derivative - Hydrochloride - Primary amine - Organosulfur compound - Organonitrogen compound - Amine - Aromatic homomonocyclic compound |
| Description | This compound belongs to the class of organic compounds known as thiophenols. These are compounds containing a thiophenol ring, which a phenol derivative obtained by replacing the oxygen atom from the hydroxyl group (attached to the benzene) by a sulfur 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 | Date | Item |
|---|---|---|---|
| Certificate of Analysis | May 20, 2026 | D136032 | |
| Certificate of Analysis | May 20, 2026 | D136032 | |
| Certificate of Analysis | May 20, 2026 | D136032 | |
| Certificate of Analysis | Jun 17, 2025 | D136032 | |
| Certificate of Analysis | Sep 06, 2024 | D136032 | |
| Certificate of Analysis | Sep 06, 2024 | D136032 | |
| Certificate of Analysis | Sep 06, 2024 | D136032 | |
| Certificate of Analysis | Sep 06, 2024 | D136032 | |
| Certificate of Analysis | Sep 06, 2024 | D136032 | |
| Certificate of Analysis | Sep 06, 2024 | D136032 | |
| Certificate of Analysis | Sep 17, 2022 | D136032 | |
| Certificate of Analysis | Sep 17, 2022 | D136032 | |
| Certificate of Analysis | Sep 17, 2022 | D136032 | |
| Certificate of Analysis | Jul 09, 2022 | D136032 | |
| Certificate of Analysis | Mar 14, 2022 | D136032 |
| Solubility | Soluble in dimethylformamide |
|---|---|
| Sensitivity | Air sensitive;Moisture sensitive |
| Melt Point(°C) | 210°C |
| Molecular Weight | 245.200 g/mol |
| XLogP3 | |
| Hydrogen Bond Donor Count | 6 |
| Hydrogen Bond Acceptor Count | 4 |
| Rotatable Bond Count | 0 |
| Exact Mass | 243.966 Da |
| Monoisotopic Mass | 243.966 Da |
| Topological Polar Surface Area | 54.000 Ų |
| Heavy Atom Count | 12 |
| Formal Charge | 0 |
| Complexity | 106.000 |
| 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 | 3 |
| 1. Qi Lai, Shaorong Huang, Yu Wu, Hu Bei, Shuilin Chen, Kun Zhang, Yuqin Xu, Xiaoyong Zhang, Guicai Sun, Yulong Ouyang. (2025) Construction of biodegradable benzobisthiazole-based conjugated polymers with pendant β-cyclodextrin for synergistic mild-temperature chemo-photothermal therapy. MATERIALS & DESIGN, [PMID:] [10.1016/j.matdes.2025.114102] |
| 2. Yongchao Hao, Jun Zhao, Hongfang Li, Min Li, Guiquan Guo, Jiangyu Zhang, Fengyan Fu. (2025) Side chain engineering for modulating hydrophilicity of benzobisthiazole-based linear conjugated polymer to improve the photocatalytic hydrogen evolution. JOURNAL OF PHOTOCHEMISTRY AND PHOTOBIOLOGY A-CHEMISTRY, [PMID:] [10.1016/j.jphotochem.2025.116530] |
| 3. Jiana Lin, Ying Chen, Gongke Li, Yuling Hu. (2025) Supramolecular calix[6]arene-COF with pocket-like cavities for host-guest recognition-based SERS detection of tryptamine and seafood freshness monitoring. FOOD CHEMISTRY, [PMID:41386090] [10.1016/j.foodchem.2025.147438] |
| 4. Ying Liu, Zhenyu Wang, Ducheng Yao, Chengcheng Chu, Zhong Chen, Wei Xiaojie, Jinguo Wang, Shun Mao. (2026) Enhanced polarization and interfacial convection of thiazole-bridged polymer-sponge architectures for high-efficiency photocatalytic water purification. WATER RESEARCH, [PMID:] [10.1016/j.watres.2026.125679] |