Dicyclohexylcarbodiimide

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MOQ : 1 Kilograms

Dicyclohexylcarbodiimide Specification

HS Code
29241990

Taste
Bitter

Application
Peptide synthesis, condensation reactions, laboratory use as a dehydrating agent

Ingredients
Dicyclohexylcarbodiimide

Appearance
White crystalline powder

Poisonous
YES

Molecular Formula
C13H22N2

Shelf Life
24 months

Purity
99%

Shape
Crystalline

Structural Formula
(C6H11N)2C

Product Type
Chemical Compound

Physical Form
Powder

Refractive Rate
Not available

Usage
Used primarily to promote amide or ester bond formation, commonly used in peptide synthesis

Density
1.325 Gram per cubic centimeter(g/cm3)

Storage
Store in tightly closed container, in a cool, dry place, protected from moisture and light

Solubility
Slightly soluble in water, readily soluble in organic solvents such as dichloromethane, chloroform, and ether

Molecular Weight
206.33 g/mol

Dicyclohexylcarbodiimide Trade Information

Minimum Order Quantity
1 Kilograms

Supply Ability
1 Kilograms Per Week

Delivery Time
1 Week

About Dicyclohexylcarbodiimide

Dicyclohexylcarbodiimide

Cas No. : 538-75-0

Packing Details : 180kg Drum

Appearance : White crystal or primrose transparent liquid

Assay : 98.50% Min

Purity Standard : 99.00% Min

Melting Point : 33-35 oC

Ignited residue : 0.10% Max

Use of Dicyclohexylcarbodiimide : Dehydration condensing agent for the synthesis of Pharmaceuticals, such as Amikacin, etc.

Key Features and Composition

Dicyclohexylcarbodiimide is recognized for its crystalline white appearance, high purity (99%), and primary use in coupling reactions, particularly peptide and ester synthesis. With a molecular weight of 206.33 g/mol and density of 1.325 g/cm3, this compound is essential in research and industrial labs, especially in India, where it is distributed, exported, and supplied by numerous manufacturers.

Applications in Organic Synthesis

DCCs primary function is to promote the formation of amide and ester bonds, making it invaluable for peptide synthesis and general condensation reactions. Its effectiveness as a dehydrating agent streamlines complex syntheses, providing researchers with reliable and efficient results.

Storage and Safety Considerations

Due to its poisonous nature, DCC must be securely stored in a tightly closed container, kept in a cool, dry, and dark environment to maintain quality over its 24-month shelf life. Always handle with protective equipment and adhere to recommended safety guidelines to minimize health hazards.

FAQs of Dicyclohexylcarbodiimide:

Q: How should Dicyclohexylcarbodiimide be stored to maintain its quality?

A: Dicyclohexylcarbodiimide should be stored in a tightly closed container, in a cool, dry place, away from moisture and direct light. Proper storage ensures its potency and extends its shelf life up to 24 months.

Q: What is the main usage of Dicyclohexylcarbodiimide in laboratories?

A: This compound is primarily used to facilitate the formation of amide or ester bonds, commonly in peptide synthesis and various condensation reactions, acting as an effective dehydrating agent in organic synthesis.

Q: When is Dicyclohexylcarbodiimide typically utilized during a chemical process?

A: DCC is mainly introduced during coupling or condensation steps, particularly in peptide synthesis, to promote the formation of chemical bonds between amino acids or other functional groups.

Q: Where can Dicyclohexylcarbodiimide be sourced in India?

A: DCC is available through multiple channels in India, including distributors, exporters, importers, manufacturers, retailers, suppliers, traders, and wholesalers specializing in laboratory chemicals.

Q: What is the process of using Dicyclohexylcarbodiimide for peptide synthesis?

A: In peptide synthesis, DCC is used to activate the carboxyl group of amino acids, enabling them to form peptide bonds with amines under controlled laboratory conditions, usually in an organic solvent.

Q: What benefits does Dicyclohexylcarbodiimide provide in organic synthesis?

A: DCC streamlines synthetic procedures by efficiently promoting bond formation, increasing reaction yields, and reducing reaction times, making it a valuable tool for chemists and researchers.

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