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Documentos Principais

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49603

Supelco

L-cistina

certified reference material, TraceCERT®, Manufactured by: Sigma-Aldrich Production GmbH, Switzerland

Sinônimo(s):

Ácido (R,R)-3,3′-ditiobis(2-aminopropiônico)

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About This Item

Fórmula linear:
[-SCH2CH(NH2)CO2H]2
Número CAS:
56-89-3
Peso molecular:
240.30
Beilstein:
1728094
Número CE:
200-296-3
Número MDL:
MFCD00064228
Código UNSPSC:
41116107
eCl@ss:
32160406
ID de substância PubChem:
329757485
Número E:
E921
NACRES:
NA.24

grau

certified reference material
TraceCERT®

Nível de qualidade

300

linha de produto

TraceCERT®

classe(s) química(is) do analito

amino acids, peptides, proteins

fabricante/nome comercial

Manufactured by: Sigma-Aldrich Production GmbH, Switzerland

condição de armazenamento

under inert gas

técnica(s)

HPLC: suitable
gas chromatography (GC): suitable

pf

>240 °C (dec.) (lit.)

aplicação(ões)

cleaning products
cosmetics
flavors and fragrances
food and beverages
personal care

Formato

neat

cadeia de caracteres SMILES

N[C@@H](CSSC[C@H](N)C(O)=O)C(O)=O

InChI

1S/C6H12N2O4S2/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)/t3-,4-/m0/s1

chave InChI

LEVWYRKDKASIDU-IMJSIDKUSA-N

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Descrição geral

L-Cystine belongs to the amino acid group and is found to be optically active due the presence of chiral centers and a wide range of hydrogen bonding network, which tends to enhance its optical properties. It can serve as an important source of L-cysteine and other sulfur containing amino acids, thus acting like a substitute for L-methionine.
This certified reference material (CRM) is produced and certified in accordance with ISO/IEC 17025 and ISO 17034. This CRM is traceable to primary material from an NMI, e.g. NIST or NMIJ.
Certified content by quantitative NMR incl. uncertainty and expiry date are given on the certificate.
Download your certificate at: http://www.sigma-aldrich.com.

Check out the entire portfolio of our amino acids certified reference materials (CRM)

Aplicação

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Embalagem

Bottomless glass bottle. Contents are inside inserted fused cone.

Informações legais

TraceCERT is a registered trademark of Merck KGaA, Darmstadt, Germany

Código de classe de armazenamento

11 - Combustible Solids

Classe de risco de água (WGK)

WGK 1

Ponto de fulgor (°F)

Not applicable

Ponto de fulgor (°C)

Not applicable

Equipamento de proteção individual

Eyeshields, Gloves, type N95 (US)

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Certificados de análise (COA)

Lot/Batch Number

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Supelco

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Supelco

76523

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Doping effect of l-cystine on structural, UV?visible, SHG efficiency, third order nonlinear optical, laser damage threshold and surface properties of cadmium thiourea acetate single crystal
Azhar.M.S, et al.
Optics & Laser technology, 87, 11-16 (2017)
Renal Transport of Organic Substances (2012)
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Protein action in nature is generally controlled by the amount of protein produced and by chemical modification of the protein, and both are often perturbed in cancer. The amino acid side chains and the peptide and disulphide bonds that bind
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In the 70s, the amino acid taurine was found essential for photoreceptor survival. Recently, we found that taurine depletion can also trigger retinal ganglion cell degeneration both in vitro and in vivo. Therefore, evaluation of taurine levels could be a
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Protocolos

GC Analysis of Amino Acids (as TBDMS Derivatives) on SLB®-5ms (20 m x 0.18 mm I.D., 0.18 μm), Fast GC Analysis

Separation of L-Alanine; Glycine; L-Valine; L-Leucine; L-Isoleucine; L-Proline; L-Methionine; L-Serine; L-Threonine; L-Phenylalanine; L-Aspartic acid; L-4-Hydroxyproline; L-Cysteine; L-Glutamic acid; L-Asparagine; L-Lysine; L-Glutamine; L-Histidine; L-Tyrosine; L-Tryptophan; L-Cystine

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