Structure of L Lysine Acetate CAS 52315 92 1 - L-Lysine Acetate CAS 52315-92-1

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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