Identification

CAS Number

52315-92-1

Name

L-Lysine Acetate

Synonyms

2,6-diaminohexanoic acid acetate
2,6-Diaminohexansäureacetat
acide 2,6-diaminohexanoïque – acide acétique (1:1)
Acide acétique – lysine (1:1) [French] [ACD/IUPAC Name]
Lysinacetat (1:1) [German] [ACD/IUPAC Name]
Lysine Acetate [USP]
Lysine acetate (1:1) [ACD/IUPAC Name]
Lysine acetate (USP)
Lysine, acetate (1:1) [ACD/Index Name]
112523-77-0 [RN]
52315-76-1 [RN]
52315-92-1 [RN]
84222-88-8 [RN]
acetic acid and 2,6-diaminohexanoic acid
ACETIC ACID; LYSINE
L-Lysine acetate
L-Lysine acetate (JP17)
L-Lysine acetate salt
L-Lysine monoacetate
MFCD00039069 [MDL number]

SMILES

CC(=O)O.C(CCN)CC(C(=O)O)N

StdInChI

InChI=1S/C6H14N2O2.C2H4O2/c7-4-2-1-3-5(8)6(9)10;1-2(3)4/h5H,1-4,7-8H2,(H,9,10);1H3,(H,3,4)

StdInChIKey

RRNJROHIFSLGRA-UHFFFAOYSA-N

Molecular Formula

C8H18N2O4

Molecular Weight

206.240

MDL Number

MFCD00039069 

Properties

Appearance

White crystals or White crystalline Powder

Safety Data

RIDADR 

NONH for all modes of transport

WGK Germany

3

Specifications and Other Information of Our L-Lysine Acetate CAS 52315-92-1

Identification Methods

HNMR, HPLC

Assay

98.5%～101.5%

PH

6.5～7.5

Specific Optical Rotation

+8.4° ～＋9.9°

State of Solution

≥95.0%

Chloride(Cl)

≤200ppm

Ammonium(NH4)

≤200ppm

Sulfate(SO4)

≤200ppm

Iron(Fe)

≤10ppm

Heavy Metals(Pb)

≤10ppm

Loss on Drying

≤0.2%

Residue on Ignition

≤0.1%

Other amino acids (TLC)

≤0.5%

Bacteria

<1000cfu/g

Yeasts and molds

<100cfu/g

Pseudomonas aeruginosa

Not detectable in lg

Staphylococus aureus

Not detectable in lg

Salmonella

Not detectable in lg

Escherichia coli

Not detectable in lg

Shelf Life

2 years

Storage

Under room temperature away from light

Known Application

Lysine acetic acid is one of the essential amino acids in the human body, with nutritional benefits in supplementing protein. In medicine, it can be used to formulate amino acid injections and oral preparations. It is also employed as an adjunct in diuretics, treating lead poisoning caused by decreased chloride in the blood. Additionally, it can form salts with acidic drugs (such as salicylic acid) to alleviate adverse reactions.

This product is developed by our R&D company Apnoke Scientific Ltd (http://www.apnoke.com/).

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