Structure

Fmoc-Cys(Trt)-OH

CAS
103213-32-7
Catalog Number
ACM103213327-1
Category
Amino Acids
Molecular Weight
585.71
Molecular Formula
C37H31NO4S

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Specification

Description
High purity Fmoc-protected amino acid for research and process production of peptides, with very low levels of dipeptide, free-amino acids and acetic acid impurities. The standard derivative for Fmoc SPPS of peptides containing Cys. The Trt group is removed with 95% TFA containing 1-5% TIS. Ideally, this derivative should be introduced using the symmetrical anhydride or DIPCDI/HOBt activation to minimize enantiomerization. If activation with uronium or phosphonium reagents, such as HBTU or PyBOP, is to be employed, it is strongly recommended that collidine is used as the base , as this has been shown to significantly reduce loss of optical integrity during coupling.
Synonyms
Fmoc-Cys(Trt)-OH, N-α-Fmoc-S-trityl-L-cysteine
InChI
1S/C37H31NO4S/c39-35(40)34(38-36(41)42-24-33-31-22-12-10-20-29(31)30-21-11-13-23-32(30)33)25-43-37(26-14-4-1-5-15-26,27-16-6-2-7-17-27)28-18-8-3-9-19-28/h1-23,33-34H,24-25H2,(H,38,41)(H,39,40)/p-1/t34-/m0/s1
InChI Key
KLBPUVPNPAJWHZ-UMSFTDKQSA-M
Melting Point
164-175℃
Application
Peptide synthesis.
Assay
≥98% (TLC)
≥98.0% (acidimetric)
≥99.0% (HPLC)
Form
powder
MDL Number
MFCD00038538
Quality Level
400
Reaction Suitability
reaction type: Fmoc solid-phase peptide synthesis
Storage Temperature
-20℃(-15℃to -25℃)
Type
Unlabeled Standard Amino Acids, Cysteine (Cys)
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