lauroyl lysine

L-lysine, N6-(1-oxododecyl)-

CAS: 52315-75-0 C18 H36 N2 O3 MW: 328.49652000

Identification

Namelauroyl lysine
IUPAC(2S)-2-amino-6-(dodecanoylamino)hexanoic acid
CAS Number52315-75-0
EINECS257-843-4
FDA UNII113171Q70B
Molecular FormulaC18 H36 N2 O3
Molecular Weight328.49652000
MDL NumberMFCD00216730
Nikkaji NumberJ94.766K

Regulatory

Physical Properties

Assay 95.00 to 100.00
Food Chemicals Codex Listed No
Boiling Point 527.00 to 528.00 °C. @ 760.00 mm Hg (est)
Flash Point 524.00 °F. TCC ( 273.10 °C. ) (est)
logP (o/w) 4.134 (est)
Soluble in water, 1.812 mg/L @ 25 °C (est)

Cosmetic Information

CosIngcosmetic data
Cosmetic Useshair conditioning

No sensory data available

Safety Information

Oral/Parenteral ToxicityNot determined
Dermal ToxicityNot determined
Inhalation ToxicityNot determined

GHS Classification

['GHS Classification in accordance with 29 CFR 1910 (OSHA HCS)', 'GHS Label elements, including precautionary statements']

Safety in Use

Categorycosmetic agents
Recommendation for lauroyl lysine usage levels up tonot for fragrance use.
Recommendation for lauroyl lysine flavor usage levels up tonot for flavor use.

Jiangyin Healthway International Trade Co., Ltd

Independent Ingredients Supplier

We provide custom synthesis and contract manufacturing from milligrams to metric tonnes.

View All Website 86-510-86023169 info@healthwaychem.com

Potential Uses

viscosity controlling agents

Natural Occurrence

not found in nature

Synonyms

(2S)-2- amino-6-(dodecanoylamino)hexanoic acid N6- dodecanoyl-L-lysine dodecyl lysine N6-(1-oxo dodecyl)-L-lysine N-6-(1-oxo dodecyl)-laevo-lysine N6- lauroyl-L-lysine lauryl lysine L- lysine, N6-(1-oxododecyl)- PubMed: Improved initial burst of estradiol organogel as long-term in situ drug delivery implant: formulation, in vitro and in vivo characterization. PubMed: Low-molecular-weight gelators based on N(alpha)-acetyl-N(epsilon)-dodecyl-L-lysine and their amphiphilic gelation properties. PubMed: Efficient Nepsilon-lauroyl-L-lysine production by recombinant epsilon-lysine acylase from Streptomyces mobaraensis. PubMed: Cationic surfactants from lysine: synthesis, micellization and biological evaluation. PubMed: Supramolecular gels formed by amphiphilic low-molecular-weight gelators of N alpha,N epsilon-diacyl-L-lysine derivatives. PubMed: A novel acylase from Streptomyces mobaraensis that efficiently catalyzes hydrolysis/synthesis of capsaicins as well as N-acyl-L-amino acids and N-acyl-peptides. PubMed: Effect of ion and surfactant choice on the recovery of a histidine-tagged protein from tobacco extract using foam fractionation. PubMed: L-lysine based gemini organogelators: their organogelation properties and thermally stable organogels. PubMed: A family of low-molecular-weight hydrogelators based on L-lysine derivatives with a positively charged terminal group. PubMed: N-terminal fatty acid substitution increases the leishmanicidal activity of CA(1-7)M(2-9), a cecropin-melittin hybrid peptide. PubMed: Myristoylated src-oncogene products are potently detected by the monoclonal antibody to the NH2-terminal myristoyl-Gly-Ser-Ser-Lys src-peptide. PubMed: Attachment of immunoglobulin to liposomal membrane via protein carbohydrate. PubMed: Arrangement of subunit IV in beef heart cytochrome c oxidase probed by chemical labeling and protease digestion experiments. PubMed: Influence of chemical modification of N alpha-cocoyl-L-arginine ethyl ester on its hepatitis B surface antigen-inactivating effect. PubMed: Determination of bioavailability of some long-chain N-substituted derivatives of L-methionine and L-lysine.