693-57-2 | 12-Aminododecanoic acid

Packsize	Purity	Availability	Price	Discounted Price
5g	95%	in stock	$14.00	$10.00
25g	95%	in stock	$37.00	$26.00
100g	95%	in stock	$99.00	$69.00
500g	95%	in stock	$165.00	$116.00

Description

• Catalog Number: AB57737
• Chemical Name: 12-Aminododecanoic acid
• CAS Number: 693-57-2
• Molecular Formula: C12H25NO2
• Molecular Weight: 215.3324
• MDL Number: MFCD00008153
• SMILES: NCCCCCCCCCCCC(=O)O

Computed Properties

• Complexity: 149
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 15
• Hydrogen Bond Acceptor Count: 3
• Hydrogen Bond Donor Count: 2
• Rotatable Bond Count: 11
• XLogP3: -0.5

Literature

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  Bioconjugate chemistry 20120718

• Multi-dye theranostic nanoparticle platform for bioimaging and cancer therapy.

  International journal of nanomedicine 20120101

• Synthesis and biological evaluation of fatty acyl ester derivatives of 2',3'-didehydro-2',3'-dideoxythymidine.

  Bioorganic & medicinal chemistry letters 20110401

• The role of surface charge on the uptake and biocompatibility of hydroxyapatite nanoparticles with osteoblast cells.

  Nanotechnology 20110311

• Chemoenzymatic synthesis and chemical recycling of poly(ester-urethane)s.

  International journal of molecular sciences 20110101

• [Simultaneous determination of berberine, palmatine, matrine, catechin and baicalin in Funing Shuan by micellar electrokinetic capillary chromatography-electrospray ionization mass spectrometry].

  Se pu = Chinese journal of chromatography 20100701

• High yield synthesis of 12-aminolauric acid by 'enzymatic transcrystallization' of omega-laurolactam using omega-laurolactam hydrolase from Acidovorax sp. T31.

  Bioscience, biotechnology, and biochemistry 20090501

• The screening, characterization, and use of omega-laurolactam hydrolase: a new enzymatic synthesis of 12-aminolauric acid.

  Bioscience, biotechnology, and biochemistry 20080801

• Molecular interactions alter clay and polymer structure in polymer clay nanocomposites.

  Journal of nanoscience and nanotechnology 20080401

• The impact of montmorillonite clay addition on the in vitro wear resistance of a glass-ionomer restorative.

  Journal of dentistry 20070401

• Self-assembled monolayers of alkanoic acids on the native oxide surface of SS316L by solution deposition.

  Langmuir : the ACS journal of surfaces and colloids 20070227

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  Journal of nanoscience and nanotechnology 20061201

• The influence of montmorillonite clay reinforcement on the performance of a glass ionomer restorative.

  Journal of dentistry 20061101

• Adsorption of fluorescently labeled protein residues on poly(ethylene-co-acrylic acid) films modified with affinity functionalities.

  Colloids and surfaces. B, Biointerfaces 20060701

• Structure-activity relationship study on a simple cationic peptide motif for cellular delivery of antisense peptide nucleic acid.

  Journal of medicinal chemistry 20051020

• A unidirectional crosslinking strategy for HIV-1 protease dimerization inhibitors.

  Bioorganic & medicinal chemistry letters 20040816