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Key Documents

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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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1 EA
¥17,995.25

¥17,995.25

Estimated to ship on2025年5月30日Details

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¥17,995.25

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

¥17,995.25

Estimated to ship on2025年5月30日Details

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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

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MOPS

assay

≥99.5% (titration)

assay

≥99.5% (titration)

assay

≥99.5% (titration)

assay

-

Quality Level

200

Quality Level

200

Quality Level

400

Quality Level

100

form

crystalline powder

form

powder or crystals

form

powder

form

crystalline powder (Fine)

application(s)

clinical research
diagnostic assay manufacturing
life science and biopharma

application(s)

-

application(s)

diagnostic assay manufacturing

application(s)

-

storage temp.

room temp

storage temp.

-

storage temp.

room temp

storage temp.

-

Other Notes

Synthesis of site-specific biotinylated probes[1]

related product

Product No.
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 Information

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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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