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8.52100

Sigma-Aldrich

Fmoc-Lys(biotinyl-ε-aminocaproyl)-OH

Novabiochem®

Synonym(s):

Fmoc-Lys(biotinyl-ε-aminocaproyl)-OH, N-α-Fmoc-N-ε-(biotinylcaproyl)-L-lysine

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About This Item

Empirical Formula (Hill Notation):
C37H49N5O7S
CAS Number:
Molecular Weight:
707.88
UNSPSC Code:
12352209

Quality Level

product line

Novabiochem®

assay

≥90.0% (HPLC)
≥98% (TLC)

form

powder

reaction suitability

reaction type: Fmoc solid-phase peptide synthesis

manufacturer/tradename

Novabiochem®

application(s)

peptide synthesis

functional group

biotin

storage temp.

2-30°C

General description

A modified lysine derivative for the preparation of biotin-labeled peptides by Fmoc SPPS, in which the biotin is separated from the lysine side-chain by a 6 C-atom spacer.

Associated Protocols and Technical Articles
Cleavage and Deprotection Protocols for Fmoc SPPS
Biotinylation Reagents for Peptide Synthesis

Linkage

Replaces: 04-12-1243

Analysis Note

Color (visual): white to slight yellow to beige
Appearance of substance (visual): powder
Identity (IR): passes test
Optical rotation α 25/D (c=1 in DMF): +11.5 - +16.0 °
Purity (TLC(CMA2)): ≥ 98 %
Assay (HPLC, area%): ≥ 90.0 % (a/a)
Solubility (100mg in 10 ml DMF): clearly soluble
This product can obtain up to 10% DMF in order to assure an ideal solubility.

To see the solvent systems used for TLC of Novabiochem® products please click here.

Legal Information

Novabiochem is a registered trademark of Merck KGaA, Darmstadt, Germany

Storage Class

11 - Combustible Solids

wgk_germany

WGK 2

flash_point_f

Not applicable

flash_point_c

Not applicable


Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Related Content

Biotin-labelled peptides have many important applications in immunology and histochemistry, such as affinity purification and FRET-based flow cytometry, solid-phase immunoassays, and receptor localization, that exploit the high affinity of streptavidin and avidin for biotin.

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

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