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NE-CARBOXYMETHYL-L-LYSINE

  • CAS：5746-04-3
  • purity：99%
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China cas 5746-04-3 factory wholesale NE-CARBOXYMETHYL-L-LYSINE at affordable price

  • Molecular Formula: C8H16N2O4
  • Molecular Weight: 204.226
  • Appearance/Colour: Off-white solid 
  • Vapor Pressure: 1.47E-08mmHg at 25°C 
  • Melting Point: 280 °C (dec.) 
  • Refractive Index: 1.518 
  • Boiling Point: 428.9 °C at 760 mmHg 
  • PKA: 2.35±0.10(Predicted) 
  • Flash Point: 213.2 °C 
  • PSA： 112.65000 
  • Density: 1.255 g/cm3 
  • LogP: 0.33400 

NE-CARBOXYMETHYL-L-LYSINE(Cas 5746-04-3) Usage

Definition

ChEBI: An L-lysine derivative with a carboxymethyl substituent at the N6-position.

InChI:InChI=1/C8H16N2O4/c9-6(8(13)14)3-1-2-4-10-5-7(11)12/h6,10H,1-5,9H2,(H,11,12)(H,13,14)/t6-/m0/s1

5746-04-3 Relevant articles

The neurotoxicity of Nε-(carboxymethyl)lysine in food processing by a study based on animal and organotypic cell culture

Gong, ZhiYong,Li, Yan,Wang, Pengcheng,Wu, Yang,Wu, Yongning,Zheng, Liangqing,liu, Yan

, (2019/12/24)

Nε-(carboxymethyl)lysine (CML) is a pote...

Simultaneous generation of acrylamide, β-carboline heterocyclic amines and advanced glycation ends products in an aqueous Maillard reaction model system

Chen, Jie,He, Zhiyong,Jiao, Ye,Li, Yong,Liu, Guoping,Qin, Fang,Quan, Wei,Wang, Zhaojun,Xue, Chaoyi,Zeng, Maomao

, (2020/07/06)

The simultaneous formation of acrylamide...

Glucoselysine is derived from fructose and accumulates in the eye lens of diabetic rats

Ohno, Rei-Ichi,Ichimaru, Kenta,Tanaka, Seitaro,Sugawa, Hikari,Katsuta, Nana,Sakake, Shiori,Tominaga, Yu-Ki,Ban, Ikuho,Shirakawa, Jun-Ichi,Yamaguchi, Yoshiki,Ito, Emi,Taniguchi, Naoyuki,Nagai, Ryoji

, p. 17326 - 17338 (2019/11/25)

Prolonged hyperglycemia generates advanc...

Novel α-Oxoamide Advanced-Glycation Endproducts within the N6-Carboxymethyl Lysine and N6-Carboxyethyl Lysine Reaction Cascades

Baldensperger, Tim,Jost, Tobias,Zipprich, Alexander,Glomb, Marcus A.

, p. 1898 - 1906 (2018/03/06)

The highly reactive α-dicarbonyl compoun...

5746-04-3 Process route

C<sub>18</sub>H<sub>34</sub>N<sub>2</sub>O<sub>5</sub>

C18 H34 N2 O5

(2S)-2-amino-6-[(carboxymethyl)amino]hexanoate
55593-17-4,5746-04-3

(2S)-2-amino-6-[(carboxymethyl)amino]hexanoate

Conditions
Conditions Yield
With hydrogenchloride; In water; at 110 ℃; for 24h;
56.3%
With hydrogenchloride; In water; at 110 ℃; for 24h;
(2S)-benzyl 6-{[(benzyloxy)-2-oxoethyl]amino}-2-{[(benzyloxy)carbonyl]amino}hexanoate
1372658-92-8

(2S)-benzyl 6-{[(benzyloxy)-2-oxoethyl]amino}-2-{[(benzyloxy)carbonyl]amino}hexanoate

(2S)-2-amino-6-[(carboxymethyl)amino]hexanoate
55593-17-4,5746-04-3

(2S)-2-amino-6-[(carboxymethyl)amino]hexanoate

Conditions
Conditions Yield
With palladium 10% on activated carbon; hydrogen; In methanol; at 20 ℃; for 24h; under 3750.38 Torr;
96%

5746-04-3 Upstream products

  • 13734-28-6
    13734-28-6

    Boc-Lys-OH

  • 79-08-3
    79-08-3

    bromoacetic acid

  • 56-87-1
    56-87-1

    L-lysine

  • 64-69-7
    64-69-7

    Iodoacetic acid

5746-04-3 Downstream products

  • 56-87-1
    56-87-1

    L-lysine

  • 3158-42-7
    3158-42-7

    (2-(2,4-dinitrophenyl)hydrazono)acetic acid

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