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analytical standard,≥99% Analytical standard for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Store at 2-8°C Ships Wet ice 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 3 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Cartap hydrochloride is the analytical standard for Cartap. This product is intended for research and analytical applications. Cartap hydrochloride is an organic nitrogen insecticide that induces significant irreversible Ca2+-dependent contractions in isolated mouse and rabbit neuronal patch preparations. It markedly elevates the levels of endogenous reactive oxygen species (ROS) in C2C12 cells.
| Sonrisas canónicas | CN(C)C(CSC(=O)N)CSC(=O)N.Cl |
|---|---|
| IUPAC Name | S-[3-carbamoylsulfanyl-2-(dimethylamino)propyl] carbamothioate;hydrochloride |
| InChIKey | MSHXTAQSSIEBQS-UHFFFAOYSA-N |
| INCHI | 1S/C7H15N3O2S2.ClH/c1-10(2)5(3-13-6(8)11)4-14-7(9)12;/h5H,3-4H2,1-2H3,(H2,8,11)(H2,9,12);1H |
| Isómeros SMILES | CN(C)C(CSC(=O)N)CSC(=O)N.Cl |
| WGK Alemania | 3 |
| RTECS | FD1225000 |
| PubChem CID | 30913 |
| Peso molecular | 273.8 |
| Beilstein | 5157539 |
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 | Organosulfur compounds |
| Clase | Thiocarbonyl compounds |
| Subclass | Thiocarbamic acid derivatives |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Thiocarbamic acid derivatives |
| Alternative Parents | Trialkylamines Organic carbonic acids and derivatives Sulfenyl compounds Organopnictogen compounds Organic zwitterions Organic oxides Organic chloride salts Hydrocarbon derivatives Carbonyl compounds |
| Molecular Framework | Aliphatic acyclic compounds |
| Substituents | Carbonic acid derivative - Tertiary amine - Thiocarbamic acid derivative - Tertiary aliphatic amine - Sulfenyl compound - Amine - Organic chloride salt - Organic salt - Organic zwitterion - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Organic oxygen compound - Organooxygen compound - Organonitrogen compound - Organic nitrogen compound - Carbonyl group - Aliphatic acyclic compound |
| Descripción | This compound belongs to the class of organic compounds known as thiocarbamic acid derivatives. These are organic compounds containing a functional group with the general structure OC(=S)NR2 or SC(=O)NR2. |
| External Descriptors | Not available |
| 1. Chen Yunhai, Zhu Xuecheng, Liu Huilin, Sun Baoguo. (2024) Multi-confinement structured carbon dots with long room temperature phosphorescence lifetime and efficiency for sensing thiram residues assisted by copper ions. MICROCHIMICA ACTA, 191 (11): (1-11). [PMID:39379669] [10.1007/s00604-024-06732-3] |
| 2. Yunhai Chen, Xuecheng Zhu, Huilin Liu, Baoguo Sun. (2025) Confining monochromophore in polymer network for fluorescence-phosphorescence dual-emission sensing of thiram. FOOD CHEMISTRY, [PMID:40784161] [10.1016/j.foodchem.2025.145825] |
| 3. Chen Yunhai, Zhu Xuecheng, Liu Huilin, Sun Baoguo. (2025) Synergistic PET/IFE-driven fluorescence-phosphorescence dual signal quenching in RTP CDs sensor for sensitive thiram monitoring in food safety. MICROCHIMICA ACTA, 192 (7): (1-10). [PMID:40506556] [10.1007/s00604-025-07291-x] |
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