(2S,2'S)-2,2'-ジアミノ-(4,4'-ジチオビス酪酸)

(2S,2'S)-2,2'-ジアミノ-(4,4'-ジチオビス酪酸) 化学構造式
626-72-2
CAS番号.
626-72-2
化学名:
(2S,2'S)-2,2'-ジアミノ-(4,4'-ジチオビス酪酸)
别名:
4,4'-ジチオビス[(S)-2-アミノブタン酸];3,3'-(ジチオビスメチレン)ビスアラニン;L-ホモシスチン;4,4'-ジチオビス[(2S)-2-アミノ酪酸];4,4'-ジチオビス[(S)-2-アミノ酪酸];(2S,2'S)-2,2'-ジアミノ-(4,4'-ジチオビス酪酸);4,4'-ジチオビス[(2S)-2-アミノブタン酸];3,3′-(ジチオビスメチレン)ビス-L-アラニン;4,4′-ジチオビス[(2S)-2-アミノ酪酸];4,4′-ジチオビス[(S)-2-アミノブタン酸];4,4′-ジチオビス[(S)-2-アミノ酪酸];4,4′-ジチオビス[(2S)-2-アミノブタン酸];3,3′-(ジチオビスメチレン)ビスアラニン;(2S,2′S)-2,2′-ジアミノ-(4,4′-ジチオビス酪酸);(2S)-2-アミノ-4-{[(3S)-3-アミノ-3-カルボキシプロピル]ジスルファニル}ブタン酸
英語名:
L-Homocystine
英語别名:
(2S,2'S)-4,4'-Disulfanediylbis(2-aMinobutanoic acid);H-HoCys-OH;(H-HCY-OH)2;(H-Hcy-OH)?;H-L-HCystine;(H-HOCYS-OH)2;H-L-HOCYSTINE;(H-Hcys-OH) 2;L-Homocystine;L-Homocystine
CBNumber:
CB5155903
化学式:
C8H16N2O4S2
分子量:
268.35
MOL File:
626-72-2.mol
MSDS File:
SDS

(2S,2'S)-2,2'-ジアミノ-(4,4'-ジチオビス酪酸) 物理性質

融点 :
281-284 °C (dec.)(lit.)
比旋光度 :
77 º (c=1% in 1N HCl)
沸点 :
507.6±50.0 °C(Predicted)
比重(密度) :
1.443±0.06 g/cm3(Predicted)
貯蔵温度 :
Keep in dark place,Inert atmosphere,Room temperature
溶解性:
H2O : 5 mg/mL (18.63 mM; ultrasonic and adjust pH to 3 with H2O)DMSO : 1 mg/mL (3.73 mM; ultrasonic and adjust pH to 5 with HCl)
外見 :
Powder
酸解離定数(Pka):
1.90±0.10(Predicted)
色:
Off-white to light yellow
BRN :
1728583
InChIKey:
ZTVZLYBCZNMWCF-WDSKDSINSA-N
CAS データベース:
626-72-2(CAS DataBase Reference)
EPAの化学物質情報:
L-Homocystine (626-72-2)

安全性情報

Sフレーズ  22-24/25
WGK Germany  3
HSコード  29309090

(2S,2'S)-2,2'-ジアミノ-(4,4'-ジチオビス酪酸) 価格 もっと(18)

メーカー 製品番号 製品説明 CAS番号 包装 価格 更新時間 購入
富士フイルム和光純薬株式会社(wako) W01FLCM06106
H-HoCys-OH
626-72-2 25g ¥40000 2024-03-01 購入
富士フイルム和光純薬株式会社(wako) W01BCS4018994
(H-Homocys-OH)2
626-72-2 1g ¥29000 2024-03-01 購入
富士フイルム和光純薬株式会社(wako) W01BCS4018994
(H-Homocys-OH)2
626-72-2 5g ¥114000 2024-03-01 購入
Sigma-Aldrich Japan H6010 L-ホモシスチン ≥98% (HPLC)
L-Homocystine ≥98% (HPLC)
626-72-2 100mg ¥19600 2024-03-01 購入
Sigma-Aldrich Japan H6010 L-ホモシスチン ≥98% (HPLC)
L-Homocystine ≥98% (HPLC)
626-72-2 500mg ¥37200 2024-03-01 購入

(2S,2'S)-2,2'-ジアミノ-(4,4'-ジチオビス酪酸) 化学特性,用途語,生産方法

化学的特性

L-homocysteine is an aliphatic amino acid with the molecular formula (C8H16N2O4S2). It is a white powder with an acidic taste and is easily soluble in water. It has limited solubility in ethanol. L-homocysteine has a sulfhydryl group on its side chain, which allows it to form disulfide bonds with other L-homocysteine residues in proteins. This feature contributes to the stable three-dimensional structure of proteins. As a result, L-homocysteine finds extensive applications in industries such as pharmaceuticals, food, feed, and cosmetics.

使用

Increased levels lead to hyperhomocysteinemia; a cardiovascular risk factor in prediction of coronary heart disease as well as being associated with congenital birth defects, pregnancy complications and cancer.

合成

L-homoserine(626-72-2) is biosynthesized from L-aspartate, which is synthesized from oxaloacetate, a TCA cycle intermediate. Homoserine is activated through esterification to form the O-acetyl ester by the enzyme homoserine O-acetyltransferase. In certain organisms, including the yeast Saccharomyces cerevisiae and certain bacteria, hydrogen sulfide reacts with O-acetyl-L-homoserine, replacing the acetyl group and forming L-homocysteine.
説明図

純化方法

The acid (3g) is dissolved in freshly boiled H2O (30mL) under N2, cooled under N2 (all operations should be under N2), absolute EtOH (100mL) is added, the acid is filtered off, and a second crop is obtained by diluting the filtrate to 500mL with absolute EtOH, kept overnight in a refrigerator, filtered, washed with EtOH and dried in a vacuum. The D(R,R)-form has similar properties but is –ve in M HCl and +ve in H2O. [du Vigneaud & Patterson J Biol Chem 109 101 1935, du Vigneaud & Brown Biochemical Preparations 5 93, 95 1975, Greenstein & Winitz The Chemistry of the Amino Acids J. Wiley, Vol 3 pp 2667-2670 1961, Beilstein 4 III 1643, 4 IV 3199, Koegel et al. J Am Chem Soc 77 5708 1955.]

(2S,2'S)-2,2'-ジアミノ-(4,4'-ジチオビス酪酸) 上流と下流の製品情報

原材料

準備製品


(2S,2'S)-2,2'-ジアミノ-(4,4'-ジチオビス酪酸) 生産企業

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(2S,2'S)-2,2'-ジアミノ-(4,4'-ジチオビス酪酸)  スペクトルデータ(IR1、IR2、MS)


626-72-2((2S,2'S)-2,2'-ジアミノ-(4,4'-ジチオビス酪酸))キーワード:


  • 626-72-2
  • (2S,2'S)-2,2'-Diamino-(4,4'-dithiobisbutyric acid)
  • 3,3'-(Dithiobismethylene)bisalanine
  • 4,4'-Dithiobis[(2S)-2-aminobutanoic acid]
  • 4,4'-Dithiobis[(S)-2-aminobutanoic acid]
  • 4,4'-Dithiobis[(S)-2-aminobutyric acid]
  • (2S,2'S)-4,4'-Dithiobis[2-aMinobutanoic Acid]
  • [S-(R*,R*)]-4,4'-Dithiobis[2-aMinobutanoic Acid]
  • L-Homocystine ,99%
  • L-Homocystine,L-4,4′-Dithiobis(2-aminobutanoic acid)
  • L-HOMOCYSTINE, >=98% (HPLC)
  • (H-L-HomoCys-OH)2
  • L-Homocystine≥ 99% (Assay)
  • H-HoCys-OH L-4,4'-Dithiobis(2-aminobutanoic acid)
  • (H-HCY-OH)2
  • (H-HOCYS-OH)2
  • (H-HOMOCYS-OH)2
  • H-L-HOCYSTINE
  • L-4,4'-DITHIO-BIS(2-AMINOBUTANOIC ACID)
  • 4,4’-dithiobis[2-amino-,[s-(theta,theta)]-butanoicaci
  • (H-Hcy-OH)?
  • L-homocystine cell culture tested
  • [S-(R*,R*)]-4,4'-dithiobis[2-aminobutyric] acid
  • 2-amino-4-(3-amino-3-carboxy-propyl)disulfanyl-butanoic acid
  • H-HoCys-OH
  • (H-Hcys-OH) 2
  • L-Homocystine
  • H-L-HCystine
  • L-Homocystine USP/EP/BP
  • Butanoic acid, 4,4'-dithiobis[2-amino-, (2S,2'S)-
  • (2S)-2-amino-4-{[(3S)-3-amino-3-carboxypropyl]disulfanyl}butanoic acid
  • 4,4'-ジチオビス[(S)-2-アミノブタン酸]
  • 3,3'-(ジチオビスメチレン)ビスアラニン
  • L-ホモシスチン
  • 4,4'-ジチオビス[(2S)-2-アミノ酪酸]
  • 4,4'-ジチオビス[(S)-2-アミノ酪酸]
  • (2S,2'S)-2,2'-ジアミノ-(4,4'-ジチオビス酪酸)
  • 4,4'-ジチオビス[(2S)-2-アミノブタン酸]
  • 3,3′-(ジチオビスメチレン)ビス-L-アラニン
  • 4,4′-ジチオビス[(2S)-2-アミノ酪酸]
  • 4,4′-ジチオビス[(S)-2-アミノブタン酸]
  • 4,4′-ジチオビス[(S)-2-アミノ酪酸]
  • 4,4′-ジチオビス[(2S)-2-アミノブタン酸]
  • 3,3′-(ジチオビスメチレン)ビスアラニン
  • (2S,2′S)-2,2′-ジアミノ-(4,4′-ジチオビス酪酸)
  • (2S)-2-アミノ-4-{[(3S)-3-アミノ-3-カルボキシプロピル]ジスルファニル}ブタン酸
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