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等級
produced by Wacker Chemie AG, Burghausen, Germany
品質等級
化驗
≥98.5%
形狀
powder
光學活性
[α]/D -224 to -218°
反應適用性
reaction type: solution phase peptide synthesis
雜質
≤0.02% ammonium
≤0.2% ninhidrin positive substances (each)
≤10 ppm heavy metals
燃燒殘留物
≤0.1%
損耗
≤0.2% loss on drying
mp
>240 °C (dec.) (lit.)
負離子痕跡
chloride (Cl-): ≤200 ppm
sulfate (SO42-): ≤300 ppm
正離子痕跡
As: ≤1 ppm
Fe: ≤10 ppm
Pb: ≤5 ppm
適合性
clear, colorless for appearance of solution
SMILES 字串
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 密鑰
LEVWYRKDKASIDU-IMJSIDKUSA-N
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一般說明
L-Cystine is an amino acid mainly found in the keratin of hair.
This product is supplied from Wacker FERMOPURE® material, but is sold for R&D use only, not for drug, household or other uses.
應用
L-Cystine can be used as a starting material for the synthesis of d-biotin, aromatic-bridged cystine cyclic peptides (cystinophanes), chiral imidazolidine disulfides and biodegradable PEGylated gadolinium-diethylenetriamine pentaacetic acid (Gd-DTPA) L-cystine copolymers.
法律資訊
FERMOPURE is a registered trademark of Wacker Chemie AG
儲存類別代碼
11 - Combustible Solids
水污染物質分類(WGK)
WGK 1
閃點(°F)
Not applicable
閃點(°C)
Not applicable
其他客户在看
L-Cystine
Organic Syntheses, 5, 39-39 (1925)
Cystinophanes, a novel family of aromatic-bridged cystine cyclic peptides: synthesis, crystal structure, molecular recognition, and conformational studies.
Journal of the American Chemical Society, 120(12), 2695-2702 (1998)
Synthesis of d-biotin from L-cystine via intramolecular [3+ 2] cycloaddition
Journal of the American Chemical Society, 104(23), 6460-6462 (1982)
Synthesis of new chiral imidazolidine disulfides derived from l-cystine and their application in the enantioselective addition of diethylzinc to aldehydes
Tetrahedron Letters, 43(13), 2335-2337 (2002)
PEG-g-poly (GdDTPA-co-L-cystine): a biodegradable macromolecular blood pool contrast agent for MR imaging.
Bioconjugate Chemistry, 15(6), 1424-1430 (2004)
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