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Safety Information

285463

Sigma-Aldrich

D-Cystine

98%, for peptide synthesis

Synonym(s):

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

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About This Item

Linear Formula:
[-SCH2CH(NH2)CO2H]2
CAS Number:
349-46-2
Molecular Weight:
240.30
Beilstein:
1728093
EC Number:
206-486-2
MDL number:
MFCD00002610
UNSPSC Code:
12352209
PubChem Substance ID:
24857190
NACRES:
NA.22

product name

D-Cystine, 98%

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

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Related Categories

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

JAN Code

285463-BULK:
285463-250MG:
285463-1G:
285463-VAR:

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Certificates of Analysis (COA)

Lot/Batch Number
MKCK7886
MKCD3691
BCBS1752V
BCBN2615V
BCBM9335V

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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

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