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159247

Sigma-Aldrich

12-Aminododecanoic acid

95%

Synonym(s):

12-Aminolauric acid

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About This Item

Linear Formula:
NH2(CH2)11COOH
CAS Number:
693-57-2
Molecular Weight:
215.33
Beilstein:
907502
EC Number:
211-754-7
MDL number:
MFCD00008153
UNSPSC Code:
12352209
PubChem Substance ID:
24849801
NACRES:
NA.22

Assay

95%

form

powder or crystals

reaction suitability

reaction type: solution phase peptide synthesis

color

white to off-white

mp

185-187 °C (lit.)

application(s)

peptide synthesis

SMILES string

NCCCCCCCCCCCC(O)=O

InChI

1S/C12H25NO2/c13-11-9-7-5-3-1-2-4-6-8-10-12(14)15/h1-11,13H2,(H,14,15)

InChI key

PBLZLIFKVPJDCO-UHFFFAOYSA-N

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Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

536.0 °F - closed cup

Flash Point(C)

280 °C - closed cup

Certificates of Analysis (COA)

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Yasuhisa Asano et al.
Bioscience, biotechnology, and biochemistry, 72(8), 2141-2150 (2008-08-08)
Several omega-laurolactam degrading microorganisms were isolated from soil samples. These strains were capable of growing in a medium containing omega-laurolactam as sole source of carbon and nitrogen. Among them, five strains (T7, T31, U124, U224, and U238) were identified as
Mohamed H M Hussein et al.
Journal of surfactants and detergents, 16(2), 233-242 (2013-02-20)
Chitosan is one of the important biopolymers and it is extracted from exoskeletons of crustaceans in sea food waste. It is a suitable eco-friendly carbon steel corrosion inhibitor in acid media; the deacetylation degree of prepared chitosan is more than
K Kamio et al.
Journal of lipid research, 33(8), 1227-1232 (1992-08-01)
For preparation of an affinity ligand, an N-fatty acyl moiety of galactosylceramide (GalCer) was chemically replaced with omega-amino-fatty acid including amino-n-hexanoic acid or amino-n-dodecanoic acid to obtain omega-aminoGalCer. For the synthesis of the compound, galactosylsphingosine (GalSph) was coupled with N-trifluoroacetyl
Hiroto Hayashi et al.
International journal of molecular sciences, 12(9), 5490-5507 (2011-10-22)
Novel poly(ester-urethane)s were prepared by a synthetic route using a lipase that avoids the use of hazardous diisocyanate. The urethane linkage was formed by the reaction of phenyl carbonate with amino acids and amino alcohols that produced urethane-containing diacids and
Adam H Dowling et al.
Journal of dentistry, 34(10), 802-810 (2006-04-25)
A pristine calcium montmorillonite (Ca-MMT) and an organically modified 12-amino-dodecanoicacid treated montmorillonite (ADA-MMT) clay were evaluated to determine the reinforcement effect on the performance of a glass ionomer (GI) restorative ChemFil Superior (Dentsply DeTrey, Kanstanz, Germany) to assess the potential
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