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Merck
CN

08599

Sigma-Aldrich

N-Biotinyl-ethylenediamine

≥96.5% (HPLC)

别名:

N-(2-Aminoethyl)biotinamide

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About This Item

经验公式(希尔记法):
C12H22N4O2S · C2HF3O2
分子量:
400.42
MDL编号:
UNSPSC代码:
12352116
PubChem化学物质编号:
NACRES:
NA.32

质量水平

检测方案

≥96.5% (HPLC)

溶解性

DMSO: soluble
methanol: soluble

储存温度

2-8°C

SMILES字符串

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

应用

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

包装

Bottomless glass bottle. Contents are inside inserted fused cone.

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

Eyeshields, Gloves, type N95 (US)

法规信息

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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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