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Safety Information

73749

Sigma-Aldrich

Nα-Fmoc-Nε-biotinyl-L-lysine

≥95.0% (HPLC)

Synonym(s):

Nα-Biotinyl-Nε-Fmoc-L-lysine, Fmoc-Lys(biotinyl)-OH

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500 MG
¥58,400

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500 MG
¥58,400

About This Item

Empirical Formula (Hill Notation):
C31H38N4O6S
CAS Number:
146987-10-2
Molecular Weight:
594.72
MDL number:
MFCD00270741
UNSPSC Code:
12352209
eCl@ss:
34058011
PubChem Substance ID:
57652489
NACRES:
NA.26

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Assay

≥95.0% (HPLC)

form

powder

reaction suitability

reaction type: Fmoc solid-phase peptide synthesis

application(s)

peptide synthesis

functional group

Fmoc

SMILES string

[H][C@@]12CS[C@H](CCCCC(=O)NCCCC[C@H](NC(=O)OCC3c4ccccc4-c5ccccc35)C(O)=O)[C@]1([H])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

Related Categories

Other Notes

Synthesis of site-specific biotinylated probes[1]

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Description
Pricing

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

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

JAN Code

73749-BULK-F:
73749-500MG-F:
73749-VAR-F:

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Certificates of Analysis (COA)

Lot/Batch Number
BCBR4936V
BCBR0500V
1418732V
1380238
1345873

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M J Macielag et al.
International journal of peptide and protein research, 44(6), 582-588 (1994-12-01)
The solid-phase synthesis of two porcine motilin derivatives, specifically biotinylated on the side chain of Lys20, was accomplished by preactivation of the protected amino acids N alpha-(9-fluorenylmethoxycarbonyl)-N epsilon-biotinyl-L-lysine and N alpha-(9-fluorenylmethoxycarbonyl)-N epsilon-[N-(biotinyl)-6-aminohexanoyl]-L-lysine with BOP/HOBt/DIEA (1:1:2.5) followed by coupling to the

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