Stable Isotope Reagent Product Detail

N-Boc-L-lysine-d4

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Product Code: CS-T-103614 Stable Isotope Reagent
N-Boc-L-lysine-d4
API Family
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Product Code
CS-T-103614

N-Boc-L-lysine-d4

Stable Isotope Reagent
Stock Status: : Enquire Live

CAT No.
CS-T-103614
CAS No.
13734-28-6(unlabelled)
Molecular Formula
C₁₁H₁₈D₄N₂O₄
Molecular Weight
250.33
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There is no hazardous surcharge associated with this product.
There is no packaging charge associated with this product.
For Research Purposes only. Not for Personal use.
All compounds supplied are strictly intended for laboratory, research, analytical, and scientific use only. They are not meant for human consumption, therapeutic use, or any form of clinical application.
CAS No.
13734-28-6(unlabelled)
Product Code
CS-T-103614
M.F.
C₁₁H₁₈D₄N₂O₄
M.W.
250.33
Smiles
CC(C)(OC(N[C@H](C(O)=O)CC([2H])([2H])C([2H])([2H])CN)=O)C
Category
Stable Isotope Reagent
API Family
-
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.
Overview
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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