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15131

Sigma-Aldrich

Boc-Lys(Boc)-OSu

≥97.0% (calc. based on dry substance, C/N)

Synonym(s):

Nα,Nε-Di-Boc-L-lysine hydroxysuccinimide ester

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5 G
€139.00

€139.00

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5 G
€139.00

About This Item

Empirical Formula (Hill Notation):
C20H33N3O8
CAS Number:
30189-36-7
Molecular Weight:
443.49
Beilstein:
1559007
MDL number:
MFCD00057898
UNSPSC Code:
12352202
eCl@ss:
32160406
PubChem Substance ID:
57647321
NACRES:
NA.22

€139.00

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Quality Level

100

Assay

≥97.0% (calc. based on dry substance, C/N)

optical activity

[α]20/D −25.5±1.5°, c = 1% in DMF

reaction suitability

reaction type: Boc solid-phase peptide synthesis

application(s)

peptide synthesis

storage temp.

−20°C

SMILES string

CC(C)(C)OC(=O)NCCCC[C@H](NC(=O)OC(C)(C)C)C(=O)ON1C(=O)CCC1=O

InChI

1S/C20H33N3O8/c1-19(2,3)29-17(27)21-12-8-7-9-13(22-18(28)30-20(4,5)6)16(26)31-23-14(24)10-11-15(23)25/h13H,7-12H2,1-6H3,(H,21,27)(H,22,28)/t13-/m0/s1

InChI key

IQVLXQGNLCPZCL-ZDUSSCGKSA-N

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Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
BCCL5450
BCCH7965
BCBX4432
BCBS1634V
BCBK9642V

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Haopeng Xiao et al.
Nature communications, 9(1), 1692-1692 (2018-04-29)
Protein glycosylation is ubiquitous in biological systems and essential for cell survival. However, the heterogeneity of glycans and the low abundance of many glycoproteins complicate their global analysis. Chemical methods based on reversible covalent interactions between boronic acid and glycans

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