7274-88-6

  • Product NameD-Lysine Hydrochloride
  • Molecular FormulaC6H15ClN2O2
  • Molecular Weight182.65
  • Purity99%
  • Appearancewhite crystalline powder
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Product Details

Quick Details

  • CasNo: 7274-88-6
  • Molecular Formula: C6H15ClN2O2
  • Appearance: white crystalline powder
  • Purity: 99%

High Purity Pharma D-Lysine Hydrochloride 7274-88-6

  • Molecular Formula:C6H15ClN2O2
  • Molecular Weight:182.65
  • Appearance/Colour:white crystalline powder 
  • Vapor Pressure:0.000123mmHg at 25°C 
  • Melting Point:266 °C (dec.)(lit.) 
  • Boiling Point:311.5 °C at 760 mmHg 
  • Flash Point:142.2 °C 
  • PSA:89.34000 
  • LogP:1.72990 

D-Lysine hydrochloride(Cas 7274-88-6) Usage

Description

D-lysine hydrochloride is the hydrochloride salt of D-lysine. It contains a D-lysine. D-lysine is a kind of D-form amino acid (not the natural amino acid in organisms, which is in L-form). 

Chemical Properties

white crystalline powder

Uses

D-Lysine is used as a component of a wide array of polymers (poly-D-lysine), surfactants and biofilms to confer a positive (cationic) charge.

Definition

ChEBI: The hydrochloride salt of D-lysine.

Isomeric SMILES: C(CCN)C[C@H](C(=O)O)N.Cl  
InChIKey: BVHLGVCQOALMSV-NUBCRITNSA-N  
InChI: InChI=1S/C6H14N2O2.ClH/c7-4-2-1-3-5(8)6(9)10;/h5H,1-4,7-8H2,(H,9,10);1H/t5-;/m1./s1  

7274-88-6 Relevant articles

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

Octa-Smolin, Frescilia,Thiele, Maike,Yadav, Rohan,Platzek, André,Clever, Guido H.,Niemeyer, Jochen

supporting information, p. 6153 - 6156 (2018/10/05)

The synthesis and application of three c...

Circularly Polarized Luminescence and Dynamic Regulation Based on the co-Assembly of L/D-Lysine Hydrochloride and Photoactivated AIE Molecules

Xicheng Feng a, Liangliang Zhu b, Bingbing Yue a

Acta Chimica Sinica, 2022

Therefore, in this work, hexathiobenzene (M-1) with photoactive aggregation-induced emission (AIE) properties were used as fluorescent dyes, and chiral amino acids L/D-Lysine hydrochloride (L/D-Lys) were used as chiral templates. Supramolecular L/D-Lys@M-1 components are formed by intermolecular hydrogen bonding in a mixed solvent (N,N-dimethylformamide (DMF)/H2O).

7274-88-6 Process route

D-lysine
923-27-3,3506-25-0

D-lysine

D-lysine bis(hydrochloride)
70-53-1,617-68-5,657-26-1,657-27-2,7274-88-6,10098-89-2,10303-72-7,22834-80-6,28826-16-6,42334-88-3,68147-44-4,94706-35-1,26124-78-7

D-lysine bis(hydrochloride)

Conditions
Conditions Yield
With hydrogenchloride; In tetrahydrofuran; water; for 3h;
94.6%
α-nitrocaprolactam
6804-88-2

α-nitrocaprolactam

2,6-Diamino-hexanoic acid; hydrochloride
70-53-1,617-68-5,657-26-1,657-27-2,7274-88-6,10098-89-2,10303-72-7,22834-80-6,28826-16-6,42334-88-3,68147-44-4,94706-35-1,26124-78-7

2,6-Diamino-hexanoic acid; hydrochloride

2,6-Diamino-hexanoic acid; hydrochloride
70-53-1,617-68-5,657-26-1,657-27-2,7274-88-6,10098-89-2,10303-72-7,22834-80-6,28826-16-6,42334-88-3,68147-44-4,94706-35-1,26124-78-7

2,6-Diamino-hexanoic acid; hydrochloride

Conditions
Conditions Yield
With hydrogenchloride; (S)-1-phenyl-ethylamine; hydrogen; palladium dichloride; Product distribution; 1.) DME, 20 deg C, 5 h;
 

7274-88-6 Upstream products

  • 923-27-3
    923-27-3

    D-lysine

  • 6804-88-2
    6804-88-2

    α-nitrocaprolactam

  • 70-53-1
    70-53-1

    2,6-Diamino-hexanoic acid; hydrochloride

7274-88-6 Downstream products

  • 31202-69-4
    31202-69-4

    Nε-(tert-butoxycarbonyl)-D-lysine

  • 132718-70-8
    132718-70-8

    Boc-D-Har(NO2)-OH

  • 34404-32-5
    34404-32-5

    (R)-2-amino-6-(((benzyloxy)carbonyl)amino)hexanoic acid

  • 70671-54-4
    70671-54-4

    Nα-carbobenzoxy-D-lysine

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