CAS No.
13734-28-6(unlabelled)
Smiles
CC(C)(OC(N[C@H](C(O)=O)CC([2H])([2H])C([2H])([2H])CN)=O)C
Category
Stable Isotope Reagent
Storage Condition
Refer MSDS for complete information
IUPAC Name
Boc-Lys-OH-d4; N2-[(1,1-Dimethylethoxy)carbonyl]- L-lysine-d4; N2-Carboxy-L-lysine N2-tert-Butyl Ester-d4; (S)-6-Amino-2-(tert-butoxycarbonylamino)hexanoic Acid-d4; N-α-(tert-Butoxycarbonyl)-L-lysine-d4; N2-tert-Butoxycarbonyl-L-lysine-d4; NSC 343721-d4; Nα-BOC-L-lysine-d4; α-N-tert-Butoxycarbonyl-L-lysine-d4; α-tert-Butoxycarbonyl-L-lysine-d4;
References
Tuma, D.J. et al.: Alc. Clin. Exp. Res., 11, 579 (1987); Ohshiro, T. et al.: Appl. Microbiol. Biotechnol., 48, 546 (1997);
Synonyms
Boc-Lys-OH-d4; N2-[(1,1-Dimethylethoxy)carbonyl]- L-lysine-d4; N2-Carboxy-L-lysine N2-tert-Butyl Ester-d4; (S)-6-Amino-2-(tert-butoxycarbonylamino)hexanoic Acid-d4; N-α-(tert-Butoxycarbonyl)-L-lysine-d4; N2-tert-Butoxycarbonyl-L-lysine-d4; NSC 343721-d4; Nα-BOC-L-lysine-d4; α-N-tert-Butoxycarbonyl-L-lysine-d4; α-tert-Butoxycarbonyl-L-lysine-d4;
Application Notes
N-Boc-L-lysine-d4 is the deuterated form of N-Boc-L-lysine (B656900), which is a protected analogue of a major amino acid participating in the binding of AcH to proteins. N-Boc-L-lysine as well as other t-butoxycarbonyl (Boc) amino acids can be converted to their respective amino acids via cleavage of the urethane bond.
Hazard Compound
Refer MSDS for complete information
N-Boc-L-lysine-d4 is the deuterated form of N-Boc-L-lysine (B656900), which is a protected analogue of a major amino acid participating in the binding of AcH to proteins. N-Boc-L-lysine as well as other t-butoxycarbonyl (Boc) amino acids can be converted to their respective amino acids via cleavage of the urethane bond.
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