4538-39-0

Basic information

• Product Name: 1,10-diisocyanatodecane
• Synonyms: 1,10-diisocyanatodecane
• CAS NO: 4538-39-0
• Molecular Formula: C₁₂H₂₀N₂O₂
• Molecular Weight: 224.2994
• Mol File: 4538-39-0.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 316.7°Cat760mmHg
• Flash Point: 129.4°C
• Appearance: /
• Density: 0.97g/cm³
• Vapor Pressure: 0.000405mmHg at 25°C
• Refractive Index: 1.483
• CAS DataBase Reference: 1,10-diisocyanatodecane(CAS DataBase Reference)
• NIST Chemistry Reference: 1,10-diisocyanatodecane(4538-39-0)
• EPA Substance Registry System: 1,10-diisocyanatodecane(4538-39-0)

Safety Data

• Hazardous Substances Data: 4538-39-0(Hazardous Substances Data)

Usage

General Description

1,10-diisocyanatodecane is a chemical compound that consists of a long hydrocarbon chain with two isocyanate functional groups at the ends. It is often used in the production of polyurethane materials, where it acts as a crosslinking agent to create strong and durable polymers. 1,10-diisocyanatodecane is known for its reactivity and ability to form strong bonds with a variety of substrates, making it useful in adhesives, sealants, and coatings. However, it is also important to handle 1,10-diisocyanatodecane with caution, as it can be irritating to the skin and respiratory system, and exposure should be minimized through proper safety measures and equipment.

InChI:InChI=1/C12H20N2O2/c15-11-13-9-7-5-3-1-2-4-6-8-10-14-12-16/h1-10H2

Upstream product

• 646-25-3 diaminodecane 
• 32315-10-9 bis(trichloromethyl) carbonate 
• 4834-98-4 1,12-dodecanedioyl dichloride 
• 10471-28-0 diethyl dodecanedioate 
• 75-44-5 phosgene 
• 79568-40-4 2-Oxo-1,3-diaza-cyclotridecane-1-carbonyl chloride 
• 32625-22-2 4,5,6,7,8,9,10,11,12,13-decahydrocyclododeca[c][1,2,5]oxadiazol-N-oxide 
• 4080-98-2 dodecanedioic acid dihydrazide 
• 79568-37-9 (E)-2-Chloro-1,3-diaza-cyclotridec-2-ene-1-carbonyl chloride 
• 79568-35-7 1,3-diazacyclotridecane-1,2-diene 

Downstream Products

• 117688-71-8 C₄₆H₈₂N₈O₄ 

Relevant articles and documents

Dimeric carbamoylguanidine-type histamine H2 receptor ligands: A new class of potent and selective agonists

The bioisosteric replacement of the acylguanidine moieties in dimeric histamine H2 receptor (H2R) agonists by carbamoylguanidine groups resulted in compounds with retained potencies and intrinsic activities, but considerably improved

A family of hydrogels based on ureido-linked aminopolyol-derived amphiphiles and bolaamphiphiles: Synthesis, gelation under thermal and sonochemical stimuli, and mesomorphic characterization

This article describes the systematic preparation of a novel family of carbohydrate amphiphiles and bolaamphiphiles in which hydrophilic and hydrophobic units are connected via a ureido or bis(ureido) moiety. The sugar core is derived from aminopolyols such as D-glucamine (1), N-methyl-D-glucamine (2), or the sugar-like species tris(hydroxymethyl)aminomethane (3). The O-unprotected derivatives behave as self-organizing nonionic surfactants with good water gelation ability, which can be induced under thermal or ultra-sound-driven stimuli. In addition, some derivatives of 1 and 2, and rarely 3 also formed lyotropic liquid crystals with lamellar or hexagonal structures that exhibit low-temperature transitions.