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Safety Information

08599

Sigma-Aldrich

N-Biotinyl-ethylenediamine trifluoroacetate salt

≥96.5% (HPLC)

Synonym(s):

N-(2-Aminoethyl)biotinamide trifluoroacetate salt

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About This Item

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

Quality Level

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

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

08599-100MG:
08599-BULK:
08599-VAR:
08599-500MG:


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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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

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