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About This Item
Linear Formula:
[-SCH2CH(NH2)CO2H]2
CAS Number:
Molecular Weight:
240.30
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352209
EC Number:
206-486-2
MDL number:
Beilstein/REAXYS Number:
1728093
Product Name
D-Cystine, 98%
Quality Level
assay
98%
optical activity
[α]20/D +212°, c = 1 in 1 M HCl
reaction suitability
reaction type: solution phase peptide synthesis
mp
265 °C (dec.) (lit.)
application(s)
peptide synthesis
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-/m1/s1
InChI key
LEVWYRKDKASIDU-QWWZWVQMSA-N
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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Masashi Harada et al.
Journal of chromatography. A, 1593, 91-101 (2019-02-12)
Novel sophisticated derivatizing agents for the efficient enantioselective separation and mass spectrometric detection of d- and l-amino acids have been developed. Two new axially chiral reagents derived from 6,6'-dimethyl-2,2'-biphenyldiamine were synthesized. Their chiral separation and detection abilities were evaluated by
Theresa K Tiefenbrunn et al.
Protein science : a publication of the Protein Society, 18(5), 970-979 (2009-04-23)
The type 1 repeat domain from thrombospondin has potent antiangiogenic activity and a structurally interesting fold, making it an attractive target for protein engineering. Chemical synthesis is an attractive approach for studying protein domains because it enables the use of
Global Trade Item Number
| SKU | GTIN |
|---|---|
| 285463-1G | 04061826705216 |