Determine the necessary mass, volume, or concentration for preparing a solution.
Moligand™, ≥80% Moligand™ for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Store at -20°C Ships Ice chest + Ice pads 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.
Biological Activity
Mancozeb is a widely used fungicide that is effective against fungal diseases in most cereals, vegetables, fruits and ornamental plants. In addition, Mancozeb can cause liver damage in mice by activating the Keap1/Nrf2 signaling pathway. Mancozeb upregulates lactate dehydrogenase and cytochrome c to alter cell metabolism and induce cell death. Mancozeb has reproductive toxicity and can induce apoptosis in ovarian cells.
| Kanonisches Lächeln | C(CNC(=S)[S-])NC(=S)[S-].C(CNC(=S)[S-])NC(=S)[S-].[Mn+2].[Zn+2] |
|---|---|
| IUPAC Name | zinc;manganese(2+);N-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate |
| InChIKey | CHNQZRKUZPNOOH-UHFFFAOYSA-J |
| INCHI | 1S/2C4H8N2S4.Mn.Zn/c2*7-3(8)5-1-2-6-4(9)10;;/h2*1-2H2,(H2,5,7,8)(H2,6,9,10);;/q;;2*+2/p-4 |
| Isomere SMILES | C(CNC(=S)[S-])NC(=S)[S-].C(CNC(=S)[S-])NC(=S)[S-].[Mn+2].[Zn+2] |
| PubChem CID | 13307026 |
| Molekulargewicht | 541.08 |
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 | Organic acids and derivatives |
| Klasse | Dithiocarbamic acids and derivatives |
| Subclass | Dithiocarbamic acid esters |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Ethylene bisdithiocarbamates |
| Alternative Parents | Metallobisdithiocarbamates Organic transition metal salts Organosulfur compounds Organopnictogen compounds Organonitrogen compounds Hydrocarbon derivatives |
| Molecular Framework | Not available |
| Substituents | Ethylene bisdithiocarbamate - Metallobisdithiocarbamate - Organic transition metal salt - Organic nitrogen compound - Organopnictogen compound - Hydrocarbon derivative - Organic salt - Organosulfur compound - Organonitrogen compound - Aliphatic acyclic compound |
| Beschreibung | This compound belongs to the class of organic compounds known as ethylene bisdithiocarbamates. These are dithiocarbamic acids (or derivatives) resulting from the formal addition of a molecule of carbon disulfide to each amino group of ethylenediamine. In addition, compounds containing a 1,2-ethanediyl carbamodithioate moiety are also members of this class. |
| External Descriptors | Not available |
Find and download the COA for your product by matching the lot number on the packaging.
| Lot Number | Certificate Type | Datum | Artikel |
|---|---|---|---|
| Certificate of Analysis | Jul 25, 2026 | M649002 | |
| Certificate of Analysis | Jul 25, 2026 | M649002 | |
| Certificate of Analysis | Jul 25, 2026 | M649002 | |
| Certificate of Analysis | Jul 25, 2026 | M649002 | |
| Certificate of Analysis | Jul 25, 2026 | M649002 |
| Löslichkeit | H2O : 1 mg/mL (1.51 mM; ultrasonic and warming and heat to 80°C) DMSO : 1 mg/mL (1.51 mM; Need ultrasonic) |
|---|
| 1. Zhigang Liu, Yi Wang, Rong Deng, Liyuan Yang, Shihua Yu, Shuping Xu, Weiqing Xu. (2016) Fe3O4@Graphene Oxide@Ag Particles for Surface Magnet Solid-Phase Extraction Surface-Enhanced Raman Scattering (SMSPE-SERS): From Sample Pretreatment to Detection All-in-One. ACS Applied Materials & Interfaces, [PMID:27191584] [10.1021/acsami.6b02944] |
Our grade selection guide covers purity, stabilizer status, and application suitability for all variants in our catalog.
View Moligand™ grade guide →