Skip to Content
Merck
All Photos(1)

Documents

08599

Sigma-Aldrich

N-Biotinyl-ethylenediamine trifluoroacetate salt

≥96.5% (HPLC)

Synonym(s):

N-(2-Aminoethyl)biotinamide trifluoroacetate salt

Sign Into View Organizational & Contract Pricing
All Photos(1)

About This Item

Empirical Formula (Hill Notation):
C12H22N4O2S · C2HF3O2
CAS Number:
1217450-40-2
Molecular Weight:
400.42
MDL number:
MFCD11045268
UNSPSC Code:
12352116
PubChem Substance ID:
329748617
NACRES:
NA.32

Quality Level

100

Assay

≥96.5% (HPLC)

solubility

DMSO: soluble
methanol: soluble

storage temp.

2-8°C

SMILES string

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

InChI

1S/C12H22N4O2S.C2HF3O2/c13-5-6-14-10(17)4-2-1-3-9-11-8(7-19-9)15-12(18)16-11;3-2(4,5)1(6)7/h8-9,11H,1-7,13H2,(H,14,17)(H2,15,16,18);(H,6,7)/t8-,9-,11-;/m0./s1

InChI key

IVRQHQHWTOYIDN-GRIHUTHFSA-N

Application

Nucleophilic biotinylation reagent for the conjugation of various substrates and their identification and quantification using biotin-binding fluorescent labels

Packaging

Bottomless glass bottle. Contents are inside inserted fused cone.

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

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’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

R K Garlick et al.
The Journal of biological chemistry, 263(1), 210-215 (1988-01-05)
Three N-acyl derivatives of biotinylethylenediamine were prepared: I, biotinylamidoethyl-3-(3-[125I]iodo-4-hydroxyphenyl)propionamide; II, biotinylamidoethyl-[3H]acetamide; and III, biotinylamidoethyl-3-(3,5-[125I]diiodo-4-hydroxyphenyl)propionamid e. Each compound was combined with a large excess of avidin, yielding 1:1 molar complexes. Aside from a small fraction of each complex that dissociated more

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

Contact Technical Service