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38801

Sigma-Aldrich

N-Biotinyl-3,6,9-trioxaundecane-1,11-diamine trifluoroacetate salt solution

≥95.0% (TLC), 25 mg/mL in DMSO

Synonym(s):

N-{2-[2-(2-(2-Aminoethoxy)ethoxy)ethoxy]ethyl}biotinamide trifluoroacetate salt

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About This Item

Empirical Formula (Hill Notation):
C18H34N4O5S · C2HF3O2
CAS Number:
Molecular Weight:
532.57
MDL number:
UNSPSC Code:
12352200
PubChem Substance ID:
NACRES:
NA.32

Assay

≥95.0% (TLC)

form

liquid

concentration

25 mg/mL in DMSO

storage temp.

2-8°C

SMILES string

OC(=O)C(F)(F)F.NCCOCCOCCOCCNC(=O)CCCC[C@@H]1SCC2NC(=O)NC12

InChI

1S/C18H34N4O5S.C2HF3O2/c19-5-7-25-9-11-27-12-10-26-8-6-20-16(23)4-2-1-3-15-17-14(13-28-15)21-18(24)22-17;3-2(4,5)1(6)7/h14-15,17H,1-13,19H2,(H,20,23)(H2,21,22,24);(H,6,7)/t14-,15-,17-;/m0./s1

InChI key

DPUGAEPSVSWENG-HAGMFFOZSA-N

Application

Nucleophilic biotinylation reagent for the attachment of cell surface glycosides to ELISA-type surfaces via a hydrophilic spacer/linker.

Packaging

Bottomless glass bottle. Contents are inside inserted fused cone.
Sold on the basis of mg solution.
Product 38801-25MG-F contains 25 mg of solution (approximately 23 microliters) of a concentration of 25 mg/mL (~0.5 mg N-biotinyl-3,6,9-trioxundecane 1,11-diamine trifluoroacetate salt). Product 38801-100MG-F contains 100 mg of solution (approximately 91 microliters) of a concentration of 25 mg/mL (~2.5 mg N-biotinyl-3,6,9-trioxundecane 1,11-diamine trifluoroacetate salt).

Storage Class Code

10 - Combustible liquids

WGK

WGK 2

Flash Point(F)

188.6 °F - closed cup

Flash Point(C)

87 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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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Katherine D McReynolds et al.
Bioorganic & medicinal chemistry, 10(3), 625-637 (2002-01-30)
Interactions of recombinant gp120 (rgp120) with non-natural glycosphingolipids (GSLs) and structurally simpler analogues have been studied using a competitive adhesion assay. Conjugates of cellobiosyl ceramide and melibiosyl ceramide were synthetically prepared as water-soluble GSL analogues. These ligands were screened against

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