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

More

Less

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)

More

Less

Safety

Safety Statements: 22-24/25
WGK Germany: 3
HS Code: 29309090

More

Less

Hazard and Precautionary Statements (GHS)

More

Less

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

More

Less

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

More

Less

L-Homocystine Suppliers

Canada 1 China 194 Germany 5 India 4 Japan 2 Switzerland 4 The Netherlands 2 United Kingdom 4 United States 31 Global 247

HBCChem, Inc.

Tel: +1-510-219-6317
Fax: +1-650-486-1361
Email: sales@hbcchem.com
Country: United States
ProdList: 10648
Advantage: 60

BOC Sciences

Tel: 16314854226
Email: info@bocsci.com
Country: United States
ProdList: 9923
Advantage: 65

TargetMol Chemicals Inc.

Tel: +1-781-999-5354 +1-00000000000
Email: marketing@targetmol.com
Country: United States
ProdList: 32165
Advantage: 58

BOC Sciences

Tel: 16314854226; +16314854226
Email: inquiry@bocsci.com
Country: United States
ProdList: 19741
Advantage: 58

Accela ChemBio Inc.

Tel: +1-858-6993322
Fax: (+1)-858-876-1948
Email: info@accelachem.com
Country: United States
ProdList: 17322
Advantage: 58

Cato Research Chemicals Inc.

Tel: 020-81215950 4000-868-328
Email: customer@uwalab.com
Country: United States
ProdList: 10404
Advantage: 58

Alchem Pharmtech,Inc.

Tel: 8485655694
Email: sales@alchempharmtech.com
Country: United States
ProdList: 63687
Advantage: 58

Aladdin Scientific

Tel: +1-+1(833)-552-7181
Email: sales@aladdinsci.com
Country: United States
ProdList: 57505
Advantage: 58

TargetMol Chemicals Inc.

Tel
Email: support@targetmol.com
Country: United States
ProdList: 38632
Advantage: 58

United States Biological

Tel: --
Fax: --
Email: sales@advtechind.com
Country: United States
ProdList: 6075
Advantage: 58

Alfa Chemistry

Tel: --
Fax: --
Email: info@Alfa-Chemistry.com
Country: United States
ProdList: 6814
Advantage: 0

United States Biological

Tel: --
Fax: --
Email: chemicals@usbio.net
Country: United States
ProdList: 6214
Advantage: 80

MedChemExpress

Tel: --
Fax: --
Email: sales@medchemexpress.com
Country: United States
ProdList: 6398
Advantage: 58

Combi-Blocks Inc.

Tel: --
Fax: --
Email: sales@combi-blocks.com
Country: United States
ProdList: 6618
Advantage: 69

Riedel-de Haen AG

Tel: --
Fax: --
Country: United States
ProdList: 6773
Advantage: 87

Frontier Scientific, Inc.

Tel: --
Fax: --
Email: sales@frontiersci.com
Country: United States
ProdList: 6222
Advantage: 86

Matrix Scientific

Tel: --
Fax: --
Email: sales@matrixscientific.com
Country: United States
ProdList: 6632
Advantage: 80

Waterstone Technology, LLC

Tel: --
Fax: --
Email: sales@waterstonetech.com
Country: United States
ProdList: 6786
Advantage: 30

Chem-Impex International, Inc.

Tel: --
Fax: --
Country: United States
ProdList: 6730
Advantage: 64

HONEST JOY HOLDINGS LIMITED

Tel: --
Fax: --
Email: sales@honestjoy.cn
Country: United States
ProdList: 6675
Advantage: 54

City Chemical LLC

Tel: --
Fax: --
Email: sales@citychemical.com
Country: United States
ProdList: 6708
Advantage: 72

3B Scientific Corporation

Tel: --
Fax: --
Email: sales@3bsc.com
Country: United States
ProdList: 6718
Advantage: 47

AK Scientific, Inc.

Tel: --
Fax: --
Email: sales@aksci.com
Country: United States
ProdList: 6347
Advantage: 65

Advance Scientific & Chemical

Tel: --
Fax: --
Email: sales@advance-scientific.com
Country: United States
ProdList: 6419
Advantage: 71

Ivy Fine Chemicals

Tel: --
Fax: --
Email: sales@ivychem.com
Country: United States
ProdList: 6493
Advantage: 58

Pfaltz & Bauer, Inc.

Tel: --
Fax: --
Email: sales@pfaltzandbauer.com
Country: United States
ProdList: 6828
Advantage: 72

City Chemicals Corporation

Tel: --
Fax: --
Country: United States
ProdList: 6460
Advantage: 72

CSPS Pharmaceuticals, Inc.

Tel: --
Fax: --
Email: csps@5z.com
Country: United States
ProdList: 1244
Advantage: 73

Synthetech, Inc.

Tel: --
Fax: --
Email: customer@synthetech.com
Country: United States
ProdList: 628
Advantage: 68

Spectrum Chemicals & Laboratory Products

Tel: --
Fax: --
Email: sales@spectrumchemical.com
Country: United States
ProdList: 6699
Advantage: 77

MP Biomedicals, Inc.

Tel: --
Fax: --
Country: United States
ProdList: 6561
Advantage: 81

More

Less

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:

4-Aminobutyric acid D-2-Aminobutyric acid N-Acetyl-L-cysteine DL-Homocysteine L-Cystine DL-2-AMINOBUTYRIC ACID L-Cysteine Selenium sulfide DL-3-Aminobutyric acid Cyproterone acetate Indole-3-butyric acid DL-2-Aminobutyric acid L(+)-2-Aminobutyric acid 3-CARBOXYPROPYL DISULFIDE Butyl disulfide Methyl propyl disulfide r-Amino Butryric Acid ETHYL PROPYL DISULFIDE

(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'-Disulfanediylbis(2-aMinobutanoic 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

(2S)-2-amino-4-{[(3S)-3-amino-3-carboxypropyl]disulfanyl}butanoic acid

Butanoic acid, 4,4'-dithiobis[2-amino-, (2S,2'S)-

L-Homocystine USP/EP/BP

L Homocystine,Inhibitor,Endogenous Metabolite,LHomocystine,inhibit,L-Homocystine

L-Homocystine

Vincamine Impurity 1( Vincamine EP Impurity A )

626-72-2

C8H16N2O4S2

Unnatural Amino Acid Derivatives

Specialty Synthesis

Peptide Synthesis

Homo-Amino Acids

Amines

Intermediates & Fine Chemicals

Pharmaceuticals

Sulfur & Selenium Compounds

Amino Acids