S-Carboxymethylation of Cysteine: Chemical Information Data Base

.Name and Description	Abbrev.	Composition	Structure	Mono Mass	Average Mass
Dithiothreitol	DTT	C₄H₁₀O₂S₂		154.01222	154.3
Iodoacetic Acid	IAA	C₂H₃O₂I		185.91778	186.0
Cysteine AA Residue	Cys C	C₃H₅NOS		103.00918	103.1
S-Carboxymethylated Cysteine Residue	CMC	C₅H₇NO₃S		161.01466	161.2
Additional Reducing and S-Carboxymethylation Agents
2-Mercaptoethanol (reducing agent, DTT is a stronger reducing agent )	BME	C₂H₆OS		78.01394	78.1
Tributylphosphine (volatile reducing agent)	-	C₁₂H₂₇P		202.18504	202.3
4-Vinylpyridine (alkylating agent)	-	C₇H₇N		105.05785	105.1

TOC Introduction Reaction Method Method Notes Why Reduce? RCM Compound Data Base Order Reagents References