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L(+)-Lysine monohydrate

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L(+)-Lysine monohydrate Basic information

Product Name:
L(+)-Lysine monohydrate
Synonyms:
  • H-LYS-OH H2O
  • LYS, MONOHYDRATE
  • L(+)-2,6-DIAMINOHEXANOIC ACID
  • L(+)-2,6-DIAMINOCAPROIC ACID
  • L-(+)-2,6-DIAMINOCAPROIC ACID HYDRATE
  • L(+)-LYS
  • L-LYS H2O
  • L(+)-LYSINE HYDRATE
CAS:
39665-12-8
MF:
C6H16N2O3
MW:
164.21
EINECS:
609-735-7
Product Categories:
  • Amino acids
  • Biochemicals Found in Plants
  • Lysine [Lys, K]
  • Nutrition Research
Mol File:
39665-12-8.mol
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L(+)-Lysine monohydrate Chemical Properties

Melting point:
212-214 °C
alpha 
26.25 º (c=8, 6N HCl)
bulk density
366kg/m3
storage temp. 
Keep in dark place,Inert atmosphere,Room temperature
solubility 
H2O: soluble
form 
Crystalline Powder or Crystals
color 
White to yellow
PH
9-10.5 (20°C, 80g/L in H2O)
biological source
non-animal source
optical activity
[α]20/D +22.5±1°, c = 2% in 6 M HCl
Water Solubility 
>1500 g/L (20 ºC)
Sensitive 
Air Sensitive & Hygroscopic
Merck 
14,5636
BRN 
1722531
CAS DataBase Reference
39665-12-8(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
24/25-36/37/39-26
WGK Germany 
3
RTECS 
OL5540000
TSCA 
Yes
HS Code 
29224100

MSDS

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L(+)-Lysine monohydrate Usage And Synthesis

Chemical Properties

white to slightly yellow crystalline powder

Uses

L-Lysine Monohydrate can be used to study the impacts of the disease from E.coli infection and benefits of preventive consumption of a stimulator of homeopathic immunity

General Description

L-Lysine is an amino acid with a basic side chain and is amphipathic in nature. It has a protonated alkyl amino group and is fully protonated at physiological pH. L-lysine mainly participates in electrostatic interactions in proteins.

Biochem/physiol Actions

L-Lysine is an essential proteinogenic α amino acid used in a wide range of applications including as a non-animal sourced supplement in cell culture media, a substrate of enzymes such as L-lysine oxidase (EC 1.4.3.14), a component of poly-lysine polymers, and a substrate for oxidation and glycation mechanism studies.

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