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Merck
CN

900750

(4-(2-(2-(2-Aminoethoxy)ethoxy)ethoxy)phenyl)(4-(prop-2-yn-1-yloxy)phenyl)methanone HCl salt

≥95%

Synonym(s):

Amino (PEG)3 benzophenone alkyne HCl salt, Probe building block

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About This Item

Empirical Formula (Hill Notation):
C22H25NO5 · HCl
Molecular Weight:
419.90
MDL number:
MFCD31537179
UNSPSC Code:
12352200
NACRES:
NA.22

Key Documents

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Product Name

(4-(2-(2-(2-Aminoethoxy)ethoxy)ethoxy)phenyl)(4-(prop-2-yn-1-yloxy)phenyl)methanone HCl salt, ≥95%

InChI key

UHKZPTZAXVJWMN-UHFFFAOYSA-N

SMILES string

[H]Cl.O=C(C1=CC=C(OCC#C)C=C1)C2=CC=C(OCCOCCOCCN)C=C2

assay

≥95%

form

powder

reaction suitability

reaction type: click chemistry

storage temp.

−20°C

Quality Level

100

Related Categories

Application

(4-(2-(2-(2-Aminoethoxy)ethoxy)ethoxy)phenyl)(4-(prop-2-yn-1-yloxy)phenyl)methanone HCl salt is used for chemical probe synthesis, this trifunctional building block contains a light-activated benzophenone, alkyne tag, and amine synthetic handle. When appended to a ligand or pharmacophore through its PEGylated amine linker, this building block allows for UV light-induced covalent modification of a biological target with potential for downstream applications via the alkyne tag. Use alone or in parallel with other multi-functional building blocks to discover the optimal probe for your chemical biology experiments.

Other Notes


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Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

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Certificates of Analysis (COA)

Lot/Batch Number
MKCT9446

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Articles

Trifunctional Probe Building Blocks

In partnership with Pfizer chemists, we have compiled a collection of trifunctional building blocks to enable development of probes.

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