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850090-09-4

850090-09-4 Structure

850090-09-4 Structure
IdentificationBack Directory
[Name]

HO-PEG5-tBu
[CAS]

850090-09-4
[Synonyms]

HO-PEG5-tBu
OH-PEG5-TBA
850090-09-4
HO-PEG5-COOtBu
Hydroxy-PEG5-Boc
OH-PEG5-CH2CH2COOtBu
HO-PEG5-CH2CH2COOtBu
Hydroxy-PEG5-CH2CO2tBu
Hydroxy-PEG5-t-butly ester
tert-Butyl 1-hydroxy-3,6,9,12,15-pentaoxaoctadecan-18-oate
HO-PEG5-CH2CH2COOtBu
2-METHYL-2-PROPANYL 1-HYDROXY-3,6,9,12,15-PENTAOXAOCTADECAN-18-OA TE
1-Hydroxy-3,6,9,12,15-pentaoxaoctadecan-18-oic acid 1,1-dimethylethyl ester
4,7,10,13,16-Pentaoxaoctadecanoic acid, 18-hydroxy-, 1,1-dimethylethyl ester
[Molecular Formula]

C17H34O8
[MDL Number]

MFCD27977509
[MOL File]

850090-09-4.mol
[Molecular Weight]

366.45
Chemical PropertiesBack Directory
[Boiling point ]

445.4±40.0 °C(Predicted)
[density ]

1.071
[refractive index ]

n/D 1.448
[storage temp. ]

-20°C
[form ]

liquid
[pka]

14.36±0.10(Predicted)
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P280-P305+P351+P338
[HS Code ]

2918999090
Hazard InformationBack Directory
[Description]

Hydroxy-PEG5-t-butyl ester is a PEG linker containing a hydroxyl group with a t-butyl ester. The hydrophilic PEG spacer increases solubility in aqueous media. The hydroxyl group enables further derivatization or replacement with other reactive functional groups. The t-butyl protected carboxyl group can be deprotected under acidic conditions.
[Uses]

This heterobifunctional, PEGylated crosslinker features a hydroxyl group at one end and t-butyl-protected carboxylic acid at the other, which can be deprotected with acidic conditions. The hydrophillic PEG linker facilitates solubility in biological applications. Hydroxy-PEG5-t-butyl ester can be used for bioconjugation or as a building block for synthesis of small molecules, conjugates of small molecules and/or biomolecules, or other tool compounds for chemical biology and medicinal chemistry that require ligation. Examples of applications include its synthetic incorporation into antibody-drug conjugates or proteolysis-targeting chimeras (PROTAC? molecules) for targeted protein degradation.
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