22543-30-2

Basic information

• Product Name: 12-AMINO-1-DODECANOIC ACID, METHYL ESTER, HYDROCHLORIDE SALT
• Synonyms: 12-AMINO-1-DODECANOIC ACID, METHYL ESTER, HYDROCHLORIDE SALT;METHYL 12-AMINODODECANOATE, HCL;METHYL 12-AMINODODECANOATE, HYDROCHLORIDE;12-aMinododecanoic acid hydrochloride
• CAS NO: 22543-30-2
• Molecular Formula: C₁₂H₂₅NO₂*ClH
• Molecular Weight: 265.82
• Product Categories: All Aliphatics;Aliphatics
• Mol File: 22543-30-2.mol
• Article Data: 3

Chemical Properties

• Melting Point: 157-160°C
• Boiling Point: 380.6°C at 760 mmHg
• Flash Point: 184°C
• Appearance: /
• Vapor Pressure: 7.57E-07mmHg at 25°C
• Storage Temp.: -20°C Freezer
• Solubility: DMSO (Slightly), Methanol (Slightly)
• CAS DataBase Reference: 12-AMINO-1-DODECANOIC ACID, METHYL ESTER, HYDROCHLORIDE SALT(CAS DataBase Reference)
• NIST Chemistry Reference: 12-AMINO-1-DODECANOIC ACID, METHYL ESTER, HYDROCHLORIDE SALT(22543-30-2)
• EPA Substance Registry System: 12-AMINO-1-DODECANOIC ACID, METHYL ESTER, HYDROCHLORIDE SALT(22543-30-2)

Safety Data

• Hazardous Substances Data: 22543-30-2(Hazardous Substances Data)

Usage

Chemical Properties

White Solid

InChI:InChI=1/C12H25NO2.ClH/c13-11-9-7-5-3-1-2-4-6-8-10-12(14)15;/h1-11,13H2,(H,14,15);1H

Upstream product

• 693-57-2 12-Aminododecanoic acid 
• 947-04-6 2-azacyclotridecanone 
• 1395034-04-4 methyl 12-aminododecanoate acetic acid salt 
• 112-38-9 10-undecenoic acid 
• 111-81-9 Methyl 10-undecenoate 
• 14811-73-5 10-oxo-decanoic acid methyl ester 
• 22915-49-7 11-cyanoundecanoic acid methyl ester 

Downstream Products

• 4272-07-5 12-(((benzyloxy)carbonyl)amino)dodecanoic acid 
• 4271-87-8 Benzyloxycarbonyl-bis-(12-amino-dodecansaeure)-methylester 
• 4271-88-9 Benzyloxycarbonyl-bis-(12-amino-dodecansaeure)-hydrazid 

Relevant articles and documents

Divergent process for C10, C11 and C12 ω-amino acid and α,ω-dicarboxylic acid monomers of polyamides from castor oil as a renewable resource

Polyamides have great potentials for diverse applications and the present production of their monomers mostly relies on resources from fossil fuel. Starting from undecylenic acid, a natural resource, we have developed both divergent and efficient processes for C10, C11 and C 12 ω-amino acid and α,ω-dicarboxylic acid monomers of the polyamides.

Transkarbams as transdermal permeation enhancers: Effects of ester position and ammonium carbamate formation

Transkarbam 12, an ammonium carbamate formed by the reaction of dodecyl 6-aminohexanoate with carbon dioxide, is a highly active, broad-spectrum, nontoxic, and nonirritant transdermal permeation enhancer. It probably acts by a dual mechanism: a part of its activity is associated with the carbamic acid salt and/or its decomposition in the acidic stratum corneum. The ammonium ester thereby released is an active enhancer species as well, and its activity highly depends on the position of the ester group.