902586

Hydroxy-PEG4-t-butyl ester

Manufacturer: Sigma Aldrich

CAS Number: 518044-32-1

Synonym(S): tert-Butyl-1-hydroxy-3,6,9,12-tetraoxapentadecan-15-oate, HO-PEG4-CO-OtBu

Select a Size

Pack Size SKU Availability Price
1 G 902586-1-G In Stock ₹ 24,161.40

902586 - 1 G

₹ 24,161.40

In Stock

Quantity

1

Base Price: ₹ 24,161.40

GST (18%): ₹ 4,349.052

Total Price: ₹ 28,510.452

Assay

≥95%

form

liquid

reaction suitability

reagent type: cross-linking reagent

refractive index

n/D 1.4492

density

1.04746 g/mL

functional group

esterhydroxyl

storage temp.

2-8°C

SMILES string

O=C(OC(C)(C)C)CCOCCOCCOCCOCCO

InChI

1S/C15H30O7/c1-15(2,3)22-14(17)4-6-18-8-10-20-12-13-21-11-9-19-7-5-16/h16H,4-13H2,1-3H3

InChI key

FJRDXEGYAVAMLB-UHFFFAOYSA-N

Other Options

Image Product Name Manufacturer Price Range
Sigma Aldrich Fine Chemicals Biosciences Hydroxy-PEG4-t-butyl ester | 518044-32-1 | 1G
-- ₹ 29,556.70
Hydroxy-PEG-5-t-butyl ester
-- ₹ 342.24 - ₹ 82,993.20
Hydroxy-PEG4-(CH2)2-Boc
-- ₹ 1,197.84 - ₹ 18,395.40
518044-32-1 | t-Butyl 3-Hydroxy(PEG4)propoinate
-- ₹ 342.24 - ₹ 64,170.00

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Description

  • Application: 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-PEG4-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.
  • Other Notes: Recruiting cytotoxic T cells to folate-receptor-positive cancer cellsSyntheses and characterizations of novel pyrrolocoumarin probes for SNAP-tag labeling technologyHigh density orthogonal surface immobilization via photoactivated copper-free click chemistry
  • Legal Information: PROTAC is a registered trademark of Arvinas Operations, Inc., and is used under license

SAFETY INFORMATION

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable