| Identification | Back Directory | [Name]
N'-Laruoyl-L-lysine | [CAS]
52315-75-0 | [Synonyms]
52315-75-0
lauroyllysine
N6-Lauroyllysine
Nε-Lauroyllysine
-Laruoyl-L-lysine
N-LAUROYL-L-LYSINE
Nε-Lauroyl-L-Lys-OH
N-6-Lauroyl-L-lysine
N''-LARUOYL-L-LYSINE
N6-Dodecanoyl-L-lysine
N2-Dodecanoyl-L-lysine
N-ALPHA-LAUROYL-L-LYSINE
NA###N'-Laruoyl-L-lysine
n6-(1-oxododecyl)-l-lysin
N-6-(1-oxododecyl)-L-Lysine
L-Lysine, N6-(1-oxododecyl)-
N'-Laruoyl-L-lysine USP/EP/BP
(S)-6-aMino-2-dodecanaMidohexanoic acid
(2S)-2-amino-6-(lauroylamino)hexanoic acid
(2S)-2-amino-6-(dodecanoylamino)hexanoic acid
(2S)-2-azanyl-6-(dodecanoylamino)hexanoic acid | [EINECS(EC#)]
257-843-4 | [Molecular Formula]
C18H36N2O3 | [MDL Number]
MFCD00216730 | [MOL File]
52315-75-0.mol | [Molecular Weight]
328.49 |
| Questions And Answer | Back Directory | [Preparation]
The preparation of N'-Laruoyl-L-lysine is mainly achieved through a condensation reaction. In this process, amino acids and lauric acid are typically used as substrates, and the condensation reaction is carried out under enzymatic catalysis. The specific preparation process is as follows: First, amino acids and lauric acid are mixed in a certain proportion, and appropriate amounts of solvent and catalyst are added. Then, the reaction is carried out under suitable temperature and pH conditions. During the reaction, the ε-amino group of lysine undergoes a condensation reaction with the carboxyl group of lauric acid to generate N'-Laruoyl-L-lysine. |
| Chemical Properties | Back Directory | [Melting point ]
229-231 °C | [Boiling point ]
528.0±45.0 °C(Predicted) | [density ]
0.994±0.06 g/cm3(Predicted) | [vapor pressure ]
0-0Pa at 20-50℃ | [storage temp. ]
2-8°C
| [form ]
Powder | [pka]
2.53±0.24(Predicted) | [color ]
White to off-white | [Cosmetics Ingredients Functions]
HAIR CONDITIONING
VISCOSITY CONTROLLING
SKIN CONDITIONING | [Cosmetic Ingredient Review (CIR)]
N'-Laruoyl-L-lysine (52315-75-0) | [InChI]
InChI=1S/C18H36N2O3/c1-2-3-4-5-6-7-8-9-10-14-17(21)20-15-12-11-13-16(19)18(22)23/h16H,2-15,19H2,1H3,(H,20,21)(H,22,23)/t16-/m0/s1 | [InChIKey]
GYDYJUYZBRGMCC-INIZCTEOSA-N | [SMILES]
C(O)(=O)[C@H](CCCCNC(=O)CCCCCCCCCCC)N | [LogP]
1.9 at 20℃ and pH6.4 | [EPA Substance Registry System]
Lauroyl lysine (52315-75-0) |
| Hazard Information | Back Directory | [Chemical Properties]
N-(Dodecanoyl)lysine is unique in its chemical structure. The lysine portion of its molecule gives it its basic properties as an amino acid derivative, while the dodecanoyl group gives it its unique fatty chain structure. This structure makes N-(dodecanoyl)lysine unique in terms of both biological activity and chemical properties. | [Uses]
Lauroyl lysine (N6-Lauroyl-L-lysine) is a compound that can be synthesized by recombinant enzymes. After the synthase is cloned and expressed, it can be used to synthesize lauroyl lysine from specific raw materials with high yield. | [Application]
N-Lauroyl-L-lysine is a useful research chemical. | [References]
[1] Efficient Nepsilon-lauroyl-L-lysine production by recombinant epsilon-lysine acylase from Streptomyces mobaraensis DOI:10.1016/j.jbiotec.2009.03.008 |
|
| Company Name: |
AF Biochem Co., Ltd. Gold
|
| Telephone: |
+86-028-60911900 13540204019 |
| Website: |
www.afbiochem.com |
| Company Name: |
jiliang chemicals
|
| Telephone: |
21-62165282 |
| Website: |
http://www.jiliangchem.com |
|