(Boc-Cys-OH)2
| Code | Size | Price |
|---|
| CDX-B0224-G005 | 5 g | £78.00 |
Quantity:
| CDX-B0224-G025 | 25 g | £280.00 |
Quantity:
Prices exclude any Taxes / VAT
Overview
Regulatory Status: RUO
Shipping:
Ambient
Storage:
+4°C
Documents
Further Information
Alternate Names/Synonyms:
Nalp. Nalp.'-di-Boc-L-cystine; N,N'-Di(tert-butoxycarbonyl)-L-cystine; NSC 164046
Appearance:
White powder.
CAS:
10389-65-8
EClass:
32160000
Form (Short):
liquid
Handling Advice:
Keep cool and dry.Protect from light and moisture.
InChi:
InChI=1S/C16H28N2O8S2/c1-15(2,3)25-13(23)17-9(11(19)20)7-27-28-8-10(12(21)22)18-14(24)26-16(4,5)6/h9-10H,7-8H2,1-6H3,(H,17,23)(H,18,24)(H,19,20)(H,21,22)/t9-,10-/m0/s1
InChiKey:
MHDQAZHYHAOTKR-UWVGGRQHSA-N
Long Description:
Chemical. CAS: 10389-65-8. Formula: C16H28N2O8S2. MW: 440.53. Synthetic. Amino acid protected by tert-butoxycarbonyl (Boc) group. Used as a reactant in peptide synthesis. Used to obtain asymmetric cystine peptides by enzymatic catalysis with immobilized papain. Used as educt for obtaining S-isoacyl dipeptide building blocks.
MDL:
MFCD00038250
Molecular Formula:
C16H28N2O8S2
Molecular Weight:
440.53
Package Type:
Vial
Product Description:
Amino acid protected by tert-butoxycarbonyl (Boc) group. Used as a reactant in peptide synthesis. Used to obtain asymmetric cystine peptides by enzymatic catalysis with immobilized papain. Used as educt for obtaining S-isoacyl dipeptide building blocks.
Purity:
>98% (CE)
SMILES:
CC(C)(C)OC(=O)N[C@@H](CSSC[C@H](NC(=O)OC(C)(C)C)C(O)=O)C(O)=O
Solubility Chemicals:
Soluble in acetone or ethanol.
Source / Host:
Synthetic.
Transportation:
Non-hazardous
UNSPSC Category:
Biochemical Reagents
UNSPSC Number:
12352200
Use & Stability:
Stable for at least 2 years after receipt when stored at -20°C.
References
(1) O. Keller, et al.; Org. Synth. 63, 160 (1985) | (2) D.-F. Tai, et al.; Biotechnol. Lett. 15, 961 (1993) | (3) D.-F. Tai, et al.; Bioorg. Med. Chem. Lett. 5, 1475 (1995) | (4) T. Yoshiya, et al.; J. Pept. Sci. 14, 1203 (2008)
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