CAS 143-06-6

Hexamethylenediamine carbamate

Description:

Hexamethylenediamine carbamate, with the CAS number 143-06-6, is an organic compound that serves as a derivative of hexamethylenediamine and carbamic acid. It typically appears as a white crystalline solid and is soluble in water, which makes it useful in various applications, particularly in the synthesis of polyurethanes and as a curing agent in epoxy resins. The compound features both amine and carbamate functional groups, which contribute to its reactivity and ability to form hydrogen bonds, enhancing its utility in polymer chemistry. Hexamethylenediamine carbamate is known for its stability under normal conditions but may decompose upon exposure to heat or strong acids. Safety data indicates that it should be handled with care, as it may cause irritation to the skin, eyes, and respiratory system. Overall, its unique chemical structure and properties make it valuable in industrial applications, particularly in the production of materials requiring enhanced durability and flexibility.

Formula: C₇H₁₆N₂O₂

InChI: InChI=1S/C7H16N2O2/c8-5-3-1-2-4-6-9-7(10)11/h9H,1-6,8H2,(H,10,11)

InChI key: InChIKey=HDIHOAXFFROQHR-UHFFFAOYSA-N

SMILES: C(CCCCN)CNC(=O)O

Synonyms:

• (6-Aminohexyl)carbamic acid
• Carbamic acid, (6-aminohexyl)-
• Carbamic acid, N-(6-aminohexyl)-
• Cheminox AC 6
• Cheminox AC 6-66
• Cheminox AC 6C
• Cheminox AC 6F
• Diak 1
• Hexamethylenediamine carbamate
• Hmdc 1
• Hsdb 2585
• N-(6-Aminohexyl)carbamic acid
• Rhenogran HMDC 70
• Rhenogran HMDC 70/AEMD

(6-Aminohexyl)carbamic acid

CAS: 143-06-6

Formula: C₇H₁₆N₂O₂

Purity: 98%

Color and Shape: Solid

Molecular weight: 160.2141

Ref: IN-DA006WZ6

(6-Aminohexyl)Carbamic Acid

CAS: 143-06-6

(6-Aminohexyl)Carbamic Acid

Purity: 98%

Molecular weight: 160.21g/mol

Ref: 54-OR1008290

Hexamethylenediamine carbamate

CAS: 143-06-6

Hexamethylenediamine carbamate (HMDA) is a compound that is used as a cross-linking agent for polymers. It is made by reacting hexamethylene diamine with carbonyldiimidazole to form the carbamate ester. HMDA can be used in a variety of applications including in polyurethane films, coatings, and adhesives. The reaction mechanism of HMDA involves nucleophilic attack on the carbonyl group by an alcohol or amine to form an acetal or amide linkage. HMDA reacts with hydroxyl groups on polymers such as polyesters and polyacrylates to form ether linkages. This reaction can also take place with carboxyl groups on fatty acids and monocarboxylic acids to form ester linkages.

Formula: C₇H₁₆N₂O₂

Purity: Min. 95%

Color and Shape: Powder

Molecular weight: 160.21 g/mol

Ref: 3D-FH173271

(6-Aminohexyl)carbamic acid

CAS: 143-06-6

Purity: 98%;RG

Molecular weight: 160.2169952

Ref: 10-F866326