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49603

L-Cystine

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

Synonim(y):

(R,R)-3,3′-Dithiobis(2-aminopropionic acid)

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Gabaryty przesyłkiSKUDostępnośćCena netto
100 mg
Skontaktuj się z Obsługą Klienta, aby uzyskać informacje na temat dostępności
492,00 zł
369,00 zł

Informacje o tej pozycji

Wzór liniowy:
[-SCH2CH(NH2)CO2H]2
Numer CAS:
Masa cząsteczkowa:
240.30
E Number:
E921
PubChem Substance ID:
eCl@ss:
32160406
UNSPSC Code:
41116107
NACRES:
NA.24
EC Number:
200-296-3
MDL number:
Beilstein/REAXYS Number:
1728094

369,00 zł

Cena katalogowa492,00 złZaoszczędź 25%

Skontaktuj się z Obsługą Klienta, aby uzyskać informacje na temat dostępności

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Quality Level

product line

TraceCERT®

grade

certified reference material, TraceCERT®

analyte chemical class(es)

amino acids, peptides, proteins

manufacturer/tradename

Manufactured by: Sigma-Aldrich Production GmbH, Switzerland

storage condition

under inert gas

technique(s)

HPLC: suitable, gas chromatography (GC): suitable

mp

>240 °C (dec.) (lit.)

application(s)

cleaning products
cosmetics
flavors and fragrances
food and beverages
personal care

format

neat

SMILES string

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

InChI key

LEVWYRKDKASIDU-IMJSIDKUSA-N

General description

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)
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.

Application

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

Packaging

Bottomless glass bottle. Contents are inside inserted fused cone.

Legal Information

TraceCERT is a registered trademark of Merck KGaA, Darmstadt, Germany
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Ta pozycja
779539C7602C5735
L-Cystine certified reference material, TraceCERT®, Manufactured by: Sigma-Aldrich Production GmbH, Switzerland

Supelco

49603

L-Cystine

L-Cystine

SAFC

C5735

L-Cystine

application(s)

cleaning products
cosmetics
flavors and fragrances
food and beverages
personal care

application(s)

-

application(s)

peptide synthesis

application(s)

pharmaceutical (small molecule)

technique(s)

HPLC: suitable, gas chromatography (GC): suitable

technique(s)

-

technique(s)

cell culture | mammalian: suitable

technique(s)

cell culture | mammalian: suitable

format

neat

format

-

format

-

format

-

Quality Level

300

Quality Level

200

Quality Level

200

Quality Level

400

grade

certified reference material, TraceCERT®

grade

-

grade

-

grade

-

manufacturer/tradename

Manufactured by: Sigma-Aldrich Production GmbH, Switzerland

manufacturer/tradename

Wacker Chemie AG

manufacturer/tradename

-

manufacturer/tradename

-


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Klasa składowania

11 - Combustible Solids

wgk

WGK 1

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)



Certyfikaty analizy (CoA)

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Dokumenty związane z niedawno zakupionymi produktami zostały zamieszczone w Bibliotece dokumentów.

Odwiedź Bibliotekę dokumentów



Renal Transport of Organic Substances (2012)
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)
Anne C Conibear et al.
The Journal of biological chemistry, 288(15), 10830-10840 (2013-02-23)
θ-Defensins are ribosomally synthesized cyclic peptides found in the leukocytes of some primate species and have promising applications as antimicrobial agents and scaffolds for peptide drugs. The cyclic cystine ladder motif, comprising a cyclic peptide backbone and three parallel disulfide



Numer pozycji handlu globalnego

SKUNUMER GTIN
49603-1G04061834232681
49603-100MG04061832415987

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