Mancozeb - Moligand™, ≥80% , CAS No.8018-01-7

CAS: 8018-01-7 Cat. No.: M649002 Summenformel: C4H6MnN2S4・C4H6N2S4Zn Molekulargewicht: 541.08 EG-Nummer: 616-995-5 PubChem CID: 13307026
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GRADE & PURITY Moligand™ ? Moligand™ — Aladdin's line of ligands and bioactive small molecules. Use for receptor, pathway, and binding studies needing defined small-molecule tools. ≥80%
Synonyms
MANCOZEB | Mancozeb, PESTANAL(R), analytical standard | 4-?(2-?chlorophenyl)?-?3-?[3-?[4-?(2-?chlorophenyl)?benzo[f]?quinolin-?3(4H)?-?ylidene]?-?1-?propen-?1-?yl]?-Benzo[f]?quinolinium? perchlorate (1:1) | Manganese Zinc ethylenebis(dithiocarbamate) | MF
Storage
Store at -20°C
Shipped In
Ice chest + Ice pads
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Size
Deutschland (EU)
USA*
Price
Qty
500mg
M649002-500mg
Auf Bestellung · 8–12 Wochen
34,62€
1g
M649002-1g
Auf Bestellung · 8–12 Wochen
60,65€
5g
M649002-5g
Auf Bestellung · 8–12 Wochen
173,46€
25g
M649002-25g
Auf Bestellung · 8–12 Wochen
433,78€
100g
M649002-100g
Auf Bestellung · 8–12 Wochen
780,88€
Enter a quantity for the sizes you want to add.
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Why this grade

Moligand™, ≥80% Moligand™ for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

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Storage & shipping

Store at -20°C Ships Ice chest + Ice pads Check lot-specific COA for exact specifications.

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Quality documents

SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.

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Literature proof

Cited in 1 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Übersicht

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.

Specifications

Synonyme
MANCOZEB | Mancozeb, PESTANAL(R), analytical standard | 4-?(2-?chlorophenyl)?-?3-?[3-?[4-?(2-?chlorophenyl)?benzo[f]?quinolin-?3(4H)?-?ylidene]?-?1-?propen-?1-?yl]?-Benzo[f]?quinolinium? perchlorate (1:1) | Manganese Zinc ethylenebis(dithiocarbamate) | MF
Spezifikationen & Reinheit
Moligand™, ≥80%
Biochemische und physiologische Mechanismen
Mancozeb is an ethylene-bis-dithiocarbamate fungicide.
Storage
Store at -20°C
Verschickt in
Ice chest + Ice pads
Dieses Produkt erfordert Kühlkettenversand. Grundversand und andere Economy-Optionen sind nicht verfügbar.
Note
Moligand™
Aktionsart
INHIBITOR
Reinheit
≥80%
Namen und Kennungen
Kanonisches LächelnC(CNC(=S)[S-])NC(=S)[S-].C(CNC(=S)[S-])NC(=S)[S-].[Mn+2].[Zn+2]
IUPAC Namezinc;manganese(2+);N-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate
InChIKeyCHNQZRKUZPNOOH-UHFFFAOYSA-J
INCHI1S/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

Documentation

📋 Safety Data Sheet (SDS)

Comprehensive hazard, handling, storage, and regulatory compliance document.

Download SDS →

✅ Certificate of Analysis (COA)

Lot-specific quality data. Enter your lot number to retrieve the exact COA.

Look up COA →

📊 Datasheet

Quick-reference summary of product specifications and applications.

View datasheet →

🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

View spec sheet →

Advanced Data

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassOrganic acids and derivatives
KlasseDithiocarbamic acids and derivatives
SubclassDithiocarbamic acid esters
Intermediate Tree Nodes Not available
Direct ParentEthylene bisdithiocarbamates
Alternative Parents Metallobisdithiocarbamates  Organic transition metal salts  Organosulfur compounds  Organopnictogen compounds  Organonitrogen compounds  Hydrocarbon derivatives  
Molecular FrameworkNot 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
BeschreibungThis 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
3D-Struktur
Interaktives chemisches Strukturmodell





Zertifikate (CoA, COO, BSE/TSE und Analyse-Diagramm)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

5 results found

Lot NumberCertificate TypeDatumArtikel
H2631381Certificate of AnalysisJul 25, 2026 M649002
H2631382Certificate of AnalysisJul 25, 2026 M649002
H2631383Certificate of AnalysisJul 25, 2026 M649002
H2631384Certificate of AnalysisJul 25, 2026 M649002
H2631385Certificate of AnalysisJul 25, 2026 M649002
Chemische und physikalische Eigenschaften
LöslichkeitH2O : 1 mg/mL (1.51 mM; ultrasonic and warming and heat to 80°C) DMSO : 1 mg/mL (1.51 mM; Need ultrasonic)
Citations of This Product
Referenzen
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]
Lösungsrechner
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