ChemicalBook > CAS DataBase List > L-Homocystine

L-Homocystine

Product Name
L-Homocystine
CAS No.
626-72-2
Chemical Name
L-Homocystine
Synonyms
(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
Molecular Formula
C8H16N2O4S2
Formula Weight
268.35
MOL File
626-72-2.mol
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L-Homocystine Property

Melting point:
281-284 °C (dec.)(lit.)
alpha 
77 º (c=1% in 1N HCl)
Boiling point:
507.6±50.0 °C(Predicted)
Density 
1.443±0.06 g/cm3(Predicted)
storage temp. 
Keep in dark place,Inert atmosphere,Room temperature
solubility 
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)
form 
Powder
pka
1.90±0.10(Predicted)
color 
Off-white to light yellow
BRN 
1728583
InChIKey
ZTVZLYBCZNMWCF-WDSKDSINSA-N
CAS DataBase Reference
626-72-2(CAS DataBase Reference)
EPA Substance Registry System
L-Homocystine (626-72-2)
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Safety

Safety Statements 
22-24/25
WGK Germany 
3
HS Code 
29309090
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Hazard and Precautionary Statements (GHS)

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N-Bromosuccinimide Price

Sigma-Aldrich
Product number
H6010
Product name
L-Homocystine
Purity
≥98% (HPLC)
Packaging
100mg
Price
$121
Updated
2024/03/01
Sigma-Aldrich
Product number
H6010
Product name
L-Homocystine
Purity
≥98% (HPLC)
Packaging
1g
Price
$597
Updated
2024/03/01
Sigma-Aldrich
Product number
H6010
Product name
L-Homocystine
Purity
≥98% (HPLC)
Packaging
500mg
Price
$347
Updated
2024/03/01
Usbiological
Product number
H7000
Product name
L-Homocystine, 99%
Packaging
1g
Price
$330
Updated
2021/12/16
TRC
Product number
H591360
Product name
L-Homocystine
Packaging
10g
Price
$145
Updated
2021/12/16
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L-Homocystine Chemical Properties,Usage,Production

Chemical Properties

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.

Uses

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.

Definition

ChEBI: L,L-homocystine is a homocystine in which both chiral centres have L configuration. It is functionally related to a L-homocysteine. It is a tautomer of a L,L-homocystine zwitterion.

Synthesis

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.

Purification Methods

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.]

L-Homocystine Preparation Products And Raw materials

Raw materials

Preparation Products

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L-Homocystine Suppliers

Nanjing Derno Pharmaceutical Technology Co., Ltd.
Tel
025-86957866 13952093866
Fax
025-68661287
Email
sales@dernopharm.com
Country
China
ProdList
924
Advantage
58
Jia Xing Isenchem Co.,Ltd
Tel
0573-85285100 18627885956
Fax
0573-85285100
Email
isenchem@163.com
Country
China
ProdList
9513
Advantage
66
Xinxiang Junlong Biotechnology Co., Ltd
Tel
+86-15517316871 15517316871
Email
1225342923@qq.com
Country
China
ProdList
23
Advantage
58
J & K SCIENTIFIC LTD.
Tel
010-82848833 400-666-7788
Fax
86-10-82849933
Email
jkinfo@jkchemical.com
Country
China
ProdList
94657
Advantage
76
Meryer (Shanghai) Chemical Technology Co., Ltd.
Tel
021-61259108 18621169109
Fax
86-21-61259102
Email
market03@meryer.com
Country
China
ProdList
40228
Advantage
62
Energy Chemical
Tel
021-021-58432009 400-005-6266
Fax
021-58436166
Email
sales8178@energy-chemical.com
Country
China
ProdList
44688
Advantage
61
Beijing Ouhe Technology Co., Ltd
Tel
010-82967028 13552068683
Fax
+86-10-82967029
Email
2355560935@qq.com
Country
China
ProdList
12390
Advantage
60
Adamas Reagent, Ltd.
Tel
400-6009262 16621234537
Fax
021-64823266
Email
chenyj@titansci.com
Country
China
ProdList
14103
Advantage
59
Shanghai Hanhong Scientific Co.,Ltd.
Tel
021-54306202 13764082696
Email
info@hanhongsci.com
Country
China
ProdList
42958
Advantage
64
Chemsky(shanghai)International Co.,Ltd.
Tel
021-50135380
Email
shchemsky@163.com
Country
China
ProdList
283
Advantage
58
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View Lastest Price from L-Homocystine manufacturers

WUHAN FORTUNA CHEMICAL CO., LTD
Product
L-Homocystine 626-72-2
Price
US $0.00/KG
Min. Order
1KG
Purity
98.0%
Supply Ability
5000kg/month
Release date
2021-10-13
Henan Bao Enluo International TradeCo.,LTD
Product
L-Homocystine 626-72-2
Price
US $10.00/kg
Min. Order
1kg
Purity
99%
Supply Ability
500t/month
Release date
2023-08-01
Guangzhou Sunton Biotechnology Co., Ltd.
Product
L-Homocystine 626-72-2
Price
US $48.00-40.00/KG
Min. Order
1KG
Purity
99%
Supply Ability
20tons
Release date
2021-06-18

626-72-2, L-HomocystineRelated Search:


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  • Unnatural Amino Acid Derivatives
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