Structure

Fmoc-Lys(biotin)-OH

CAS
146987-10-2
Catalog Number
ACM146987102
Category
Amino Acids
Molecular Weight
594.72
Molecular Formula
C31H38N4O6S

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Specification

Description
A modified lysine derivative for the preparation of biotin-labeled peptides by Fmoc SPPS.
Synonyms
Fmoc-Lys(biotin)-OH, N-α-Fmoc-N-ε-biotinyl-L-lysine
Canonical SMILES
C1C2C(C(S1)CCCCC(=O)NCCCCC(C(=O)O)NC(=O)OCC3C4=CC=CC=C4C5=CC=CC=C35)NC(=O)N2
InChI
1S/C31H38N4O6S/c36-27(15-6-5-14-26-28-25(18-42-26)33-30(39)35-28)32-16-8-7-13-24(29(37)38)34-31(40)41-17-23-21-11-3-1-9-19(21)20-10-2-4-12-22(20)23/h1-4,9-12,23-26,28H,5-8,13-18H2,(H,32,36)(H,34,40)(H,37,38)(H2,33,35,39)/t24-,25-,26-,28-/m0/s1
InChI Key
OFIBQNGDYNGUEZ-OBXRUURASA-N
Boiling Point
936.2±65.0 ℃at 760 mmHg
Melting Point
183 ℃
Flash Point
520.0±34.3 ℃
Density
1.3±0.1 g/cm3
Application
Peptide synthesis.
Assay
≥85.0% (HPLC)
≥95% (TLC)
Exact Mass
594.251221
Form
powder
Functional Group
biotin
LogP
3.2
MDL Number
MFCD00270741
PSA
171.16
Quality Level
200
Reaction Suitability
reaction type: Fmoc solid-phase peptide synthesis
Refractive Index
1.594
Storage Temperature
2-30℃
Type
Unlabeled Standard Amino Acids, Lysine (Lys)
Vapor Pressure
0.0±0.3 mmHg at 25℃
WGK Germany
3

Upstream Synthesis Route 1

  • 105047-45-8
  • 35013-72-0
  • 146987-10-2

Reference: [1] Chemical Communications, 2006, # 7, p. 717 - 719
[2] Chemical Communications, 2017, vol. 53, # 36, p. 5020 - 5023
[3] Chemistry - A European Journal, 2017, vol. 23, # 45, p. 10906 - 10914

Upstream Synthesis Route 2

  • 105047-45-8
  • 58-85-5
  • 146987-10-2

Reference: [1] Journal of Chemical Research, 2010, # 6, p. 348 - 350

Downstream Synthesis Route 1

  • 146987-10-2
  • 576-19-2

Reference: [1] Chemical Communications, 2017, vol. 53, # 36, p. 5020 - 5023
[2] Chemistry - A European Journal, 2017, vol. 23, # 45, p. 10906 - 10914

* For details of the synthesis route, please refer to the original source to ensure accuracy.

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