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AgrochemicalsCarbendazim Impurity 4

SKU: SAC-03-D

Original price was: ₹60,000.00.Current price is: ₹50,000.00.

Name:Methyl(1-methyl benzimidazole-2-yl)Carbamate CAT. NO.:SAC-03-D CAS NO.:77106-42-4

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Description

Carbendazim Impurity 4

Chemical Name Methyl(1-methyl benzimidazole-2-yl)Carbamate
Catalog Number SAC-03-D
Parent AI Carbendazim
Synonyms Methyl (1-methyl-1H-benzimidazol-2-yl)carbamate;Methyl N-(1-methylbenzimidazol-2-yl)carbamate;Carbamic acid, (1-methyl-1H-benzimidazol-2-yl)-, methyl ester (9CI)
CAS Number 77106-42-4
Molecular Formula C10H11N3O2
Molecular Weight 205.21
Appearance NA
Melting Point 318°C
Shipping & Storage Information

 

Storage-20°C

Shipping: Free Shipping at Room Temperature in INDIA,  may vary elsewhere

Stability: Datasheet

Solubility NA
Stability Stable under recommended storage conditions
Category Agrochemical Impurity Standard/Metabolites;

Methyl(1-methyl benzimidazole-2-yl)Carbamate, a mouthful of a name, encapsulates the intriguing nature of a compound that finds applications across various fields, from agriculture to medicinal chemistry. This chemical entity, with its unique structure and versatile properties, has garnered attention for its diverse range of uses.

Structure and Composition: Methyl(1-methyl benzimidazole-2-yl)Carbamate belongs to the class of carbamates, which are organic compounds derived from carbamic acid. Its complex name can be broken down to understand its components:

  • Methyl group: A carbon atom bound to three hydrogen atoms (CH3), contributing to the compound’s organic nature.
  • Benzimidazole ring: A fused ring system containing a benzene ring fused to an imidazole ring. This confers aromaticity and structural rigidity.
  • Carbamate group: A functional group composed of a carbonyl group (C=O) and an amino group (NH2), linked to the benzimidazole ring.

Applications:

  1. Agriculture: Methyl(1-methyl benzimidazole-2-yl)Carbamate is recognized for its role in agriculture as a fungicide and nematocide. It has demonstrated efficacy in controlling various fungal diseases that affect crops, contributing to increased agricultural productivity.
  2. Medicinal Chemistry: The compound’s unique structure makes it a valuable scaffold in medicinal chemistry. Researchers have explored its potential in drug design, particularly in creating molecules with antifungal, anticancer, and anti-inflammatory properties. The benzimidazole moiety is known to exhibit biological activity, and by modifying the substituents, scientists can fine-tune the compound’s interactions with target molecules in the body.
  3. Veterinary Medicine: Methyl(1-methyl benzimidazole-2-yl)Carbamate is also used in veterinary medicine to combat parasitic infections in animals, especially helminth infections. Its mechanism of action involves disrupting the metabolism of parasites, leading to their elimination.
  4. Industrial Uses: The compound’s diverse chemical properties make it useful in various industrial applications. It can act as a catalyst in certain chemical reactions and be employed in the synthesis of other complex molecules.

Challenges and Considerations: Despite its versatility, the compound is not without challenges. Its complex synthesis can pose obstacles in large-scale production, affecting its availability and cost-effectiveness. Additionally, like many chemical agents, it requires careful handling due to its potential toxicity to non-target organisms and the environment.

Safety and Regulations: As with any chemical compound, safety is paramount. Proper handling, storage, and disposal procedures must be followed to minimize risks. Regulatory agencies in different countries provide guidelines and restrictions on the use of such compounds to ensure public health and environmental safety.

Additional information

Pack Size

50mg

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