C6727

L-Cystine dihydrochloride

from non-animal source, BioReagent, suitable for cell culture, ≥98.0% dry basis

• Synonim(y): Cystine dihydrochloride
• Wzór empiryczny (zapis Hilla): C₆H₁₂N₂O₄S₂ · 2HCl
• Numer CAS: 30925-07-6
• Masa cząsteczkowa: 313.22
• Numer WE: 250-391-9
• Numer MDL: MFCD00070399
• Kod UNSPSC: 12352209
• Identyfikator substancji w PubChem: 24892885
• NACRES: NA.26

Właściwości

• pochodzenie biologiczne: non-animal source
• Poziom jakości: 300
• linia produktu: BioReagent
• Próba: ≥98.0% dry basis
• Postać: powder or crystals
• aktywność optyczna: [α]20/D -174 to -164 °, c = 2 in 1 M HCl
• metody: cell culture | mammalian: suitable
• zanieczyszczenia: endotoxin, tested
• kolor: white to off-white
• mp: ≥211.36 °C
• rozpuszczalność: 2 M HCl: 50 mg/mL
• ślady kationów: As: ≤2 ppm; Fe: ≤30 ppm; NH₄⁺: ≤0.03%; heavy metals: ≤10 ppm
• grupa funkcyjna: carboxyl; thiol
• temp. przechowywania: room temp
• ciąg SMILES: Cl.Cl.N[C@@H](CSSC[C@H](N)C(O)=O)C(O)=O
• InChI: 1S/C6H12N2O4S2.2ClH/c7-3(5(9)10)1-13-14-2-4(8)6(11)12;;/h3-4H,1-2,7-8H2,(H,9,10)(H,11,12);2*1H/t3-,4-;;/m0../s1
• Klucz InChI: HHGZUQPEIHGQST-RGVONZFCSA-N

Opis

Opis ogólny

L-Cystine dihydrochloride is a vital component of biological systems, and its role in protein structure, redox chemistry, and cellular processes makes it a valuable tool in Biology and Chemistry research across a wide range of applications, from understanding fundamental biochemical mechanisms to drug development and nutritional research. L-Cystine is essential for studying protein structure and function. It can be used to create disulfide bonds in proteins, aiding in the formation of protein complexes and the stabilization of protein structures. This is particularly important in biotechnology and pharmaceutical research.

Zastosowanie

L-cystine dihydrochloride has been used:

• as a supplement to study homopropargylglycine update in metabolomics
• as a supplement in protein synthesis for cell biology and stem cell research
• to study the effect of lipid peroxidation and ferroptosis by regulation of cysteine and GSH levels in biochemical research

Działania biochem./fizjol.

Cystine is the dimeric form of cysteine. Cysteine is the source of disulfide linkages in proteins and has a role in sulfur transport. It undergoes rapid oxidation to form cystine at physiological pH. L-Cystine is crucial for oxygen production and low density lipoprotein modification by arterial smooth muscle cells. It also has a role in the synthesis of glutathione.

Cechy i korzyści

• High-quality compound suitable for multiple research applications
• Suitable for mammalian cell culture
• Prepared from non-animal source
• Tested for Endotoxins

Przestroga

hygroscopic

Inne uwagi

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Informacja o środkach bezpieczeństwa

• Piktogramy: GHS05
• Hasło ostrzegawcze: Danger
• Zwroty wskazujące rodzaj zagrożenia: H314
• Zwroty wskazujące środki ostrożności: P260 - P280 - P303 + P361 + P353 - P304 + P340 + P310 - P305 + P351 + P338 - P363
• Klasyfikacja zagrożeń: Eye Dam. 1 - Skin Corr. 1B
• Kod klasy składowania: 8A - Combustible, corrosive hazardous materials
• Klasa zagrożenia wodnego (WGK): WGK 1
• Temperatura zapłonu (°F): Not applicable
• Temperatura zapłonu (°C): Not applicable
• Środki ochrony indywidualnej: Eyeshields, Gloves, type N95 (US)