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Usage

Uses

Used in Pharmaceutical Applications:
DL-Lysine dihydrochloride is used as a nutritional supplement for enhancing muscle growth and improving athletic performance. It supports protein synthesis, which is crucial for muscle development and recovery.
Used in Animal Feed Production:
DL-Lysine dihydrochloride is used as an additive in animal feed to fortify it with essential amino acids. This helps in promoting the growth and overall health of animals, ensuring they receive the necessary nutrients for optimal development.
Used in Food Additives Industry:
DL-Lysine dihydrochloride is used as a food additive to enrich products with essential amino acids. This helps in improving the nutritional value of the food products and contributes to the overall health and well-being of consumers.
Used in Antiviral Treatments:
DL-Lysine dihydrochloride has been studied for its potential benefits in treating cold sores and herpes infections due to its antiviral properties. It may help in reducing the severity and duration of these viral infections, providing relief to affected individuals.

InChI:InChI=1/C6H14N2O2.2ClH/c7-4-2-1-3-5(8)6(9)10;;/h5H,1-4,7-8H2,(H,9,10);2*1H

Upstream product

• 70288-83-4 2,6-Bis(methoxycarbonylamino)hexansaeure-methylester 
• 77300-38-0 2,6-Bis(ethoxycarbonylamino)hexansaeure-ethylester 
• 29512-97-8 2,6-Dibromhexansaeure-ethylester 
• 17687-54-6 2,6-Dichlorhexansaeure-methylester 
• 77300-44-8 6-Brom-2-chlorhexansaeure-methylester 
• 657-27-2 L-Lysine hydrochloride 
• 923-27-3 D-lysine 
• 6804-88-2 α-nitrocaprolactam 
• 70-53-1 2,6-Diamino-hexanoic acid; hydrochloride 
• 4254-76-6 2,6-Diisocyanatohexansaeure-ethylester 
• 29547-05-5 2,6-Dibromhexansaeure-methylester 

Downstream Products

• 17929-90-7 3-aminoazepan-2-one 
• 687-64-9 DL-lysine methyl ester 
• 118812-46-7 DPAB-D-Lys (trans) 
• 118812-46-7 DPAB-D-Lys (cis) 
• 70-53-1 2,6-Diamino-hexanoic acid; hydrochloride 

Relevant academic research and scientific papers

Chiral Receptors for Lysine Based on Covalently Linked Bis- and Tris-binaphthylphosphoric Acids

The synthesis and application of three chiral receptors based on the covalent linkage of 1,1′-binaphthylphosphoric acids is reported. The binding of the lysine enantiomers to the chiral receptors was investigated by DOSY-NMR and NMR titrations, revealing that the bisphosphoric acid 1d acts as a highly stereoselective receptor for binding of d-lysine.

Polyamino acids functionalized by at least one hydrophobic group and the therapeutic application thereof

The invention relates to novel materials based on biodegradable polyamino acids that are useful for vectorizing active principle/s (AP). The aim of the invention is to supply a new polymeric raw material that is used for vectorizing AP and optimally fulfills all requirements concerning biocompatibility, biodegradability, the ability to be easily associated with numerous active principles or solubilize said active principles and to release the active principles in vivo. Said polymers can also be readily and economically transformed into particles vectorizing active principles according to the grafting rate of the hydrophobic groups, said particles being able to form stable aqueous colloidal suspensions. Said aim is achieved by the inventive amphiphile polyamino acids comprising aspartic and/or glutamic units that carry grafts which encompass at least one hydrophobic unit and are linked to the aspartic and/or glutamic units via a rotula containing two amide functions, more particularly via a spacer of the lysine or ornithine type. Said amide functions ensure better stability during hydrolysis than comparable products known in prior art. The invention also relates to new pharmaceutical, cosmetic, dietetic, or phytosanitary compositions based on the inventive polyamino acids.

Aminosaeuren, I. Darstellung von Aminosaeuren aus Halogencarbonsaeure-alkylestern mit Alkalimetallcyanaten

α- and ω-halo- as well as α,ω-dihalocarboxylic alkyl esters react with potassium cyanate in the presence of alcohol at 80 - 120 deg C in dipolar aprotic solvents to yield α- and ω-(alkoxycarbonylamino)- and α,ω-bis(alkoxycarbonylamino)carboxylic alkyl esters, respectively, in good yields.Hydrolytic cleavage of these mono- or diurethanes with an aqueous solution of hydrochloric acid/formic acid leads to the corresponding amino acid hydrochlorides in nearly quantitative yields.