Buy Ald-PEG4-t-butyl ester (BT-259168)

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Ald-PEG4-t-butyl ester

Catalog Number: BT-259168

CAS Number: 1415329-20-2

Molecular Formula: C15H28O7

Molecular Weight: 320.38

The product is for non-human research only. Not for therapeutic or veterinary use.

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Product Introduction

Description

Ald-PEG4-t-butyl ester is a chemical compound that belongs to the class of polyethylene glycol (PEG) derivatives. It is a versatile molecule that has found applications in various fields, including medical, environmental, and industrial research. This paper aims to provide an overview of Ald-PEG4-t-butyl ester, including its synthesis, chemical structure, biological activity, effects on cell function and signal transduction, potential therapeutic and toxic effects, and applications in different research fields. Additionally, the paper will discuss the future perspectives and challenges associated with the use of Ald-PEG4-t-butyl ester.

Properties

CAS Number

1415329-20-2

Product Name

Ald-PEG4-t-butyl ester

IUPAC Name

tert-butyl 3-[2-[2-[2-(2-oxoethoxy)ethoxy]ethoxy]ethoxy]propanoate

Molecular Formula

C15H28O7

Molecular Weight

320.38

InChI

InChI=1S/C15H28O7/c1-15(2,3)22-14(17)4-6-18-8-10-20-12-13-21-11-9-19-7-5-16/h5H,4,6-13H2,1-3H3

InChI Key

SCAAICMVIUVGGM-UHFFFAOYSA-N

SMILES

CC(C)(C)OC(=O)CCOCCOCCOCCOCC=O

Solubility

Soluble in DMSO

Synonyms

Ald-CH2-PEG4-t-butyl ester

Method of Synthesis or Extraction

Ald-Ald-PEG4-t-butyl ester4-t-butyl ester can be synthesized using different methods, including the reaction of t-butyl alcohol with Ald-PEG4-t-butyl ester4 and Ald-Cl in the presence of a base such as triethylamine. Another method involves the reaction of Ald-PEG4-t-butyl ester4 with t-butyl chloroformate and Ald-OH in the presence of a base such as pyridine. The efficiency and yield of each method depend on various factors such as the reaction conditions, the purity of the starting materials, and the expertise of the chemist. Environmental and safety considerations are also crucial when synthesizing Ald-Ald-PEG4-t-butyl ester4-t-butyl ester. The use of hazardous chemicals and solvents should be minimized, and proper disposal methods should be employed to prevent environmental pollution.

Chemical Structure and Biological Activity

Ald-Ald-PEG4-t-butyl ester4-t-butyl ester has a molecular weight of 383.5 g/mol and a chemical formula of C16H33NO6. It consists of a Ald-PEG4-t-butyl ester4 chain attached to an aldehyde group and a t-butyl ester group. The aldehyde group can react with amino groups in proteins, peptides, and other biomolecules, making Ald-Ald-PEG4-t-butyl ester4-t-butyl ester a useful tool for bioconjugation and drug delivery applications. The t-butyl ester group can be hydrolyzed under mild conditions, releasing the aldehyde group and the Ald-PEG4-t-butyl ester4 chain. Ald-Ald-PEG4-t-butyl ester4-t-butyl ester has been shown to exhibit bioactivity and potency against various biological targets, including cancer cells, bacteria, and viruses. Its mechanism of action involves the inhibition of cell proliferation, induction of apoptosis, and disruption of cell membrane integrity.

Biological Effects

Ald-Ald-PEG4-t-butyl ester4-t-butyl ester can affect cell function and signal transduction by modulating various cellular pathways, including the MAPK/ERK, PI3K/Akt, and NF-κB pathways. It can also induce oxidative stress and DNA damage, leading to cell death. The potential therapeutic and toxic effects of Ald-Ald-PEG4-t-butyl ester4-t-butyl ester depend on the dose, route of administration, and target tissue. In medical research, Ald-Ald-PEG4-t-butyl ester4-t-butyl ester has been investigated as a potential anticancer agent, drug delivery vehicle, and imaging probe. In environmental research, Ald-Ald-PEG4-t-butyl ester4-t-butyl ester has been used to study the effects of pollutants on ecosystems and to develop sustainable pollution management strategies. In industrial research, Ald-Ald-PEG4-t-butyl ester4-t-butyl ester has been employed in various manufacturing processes to improve product quality and efficiency.

Applications

In medical research, Ald-Ald-PEG4-t-butyl ester4-t-butyl ester has been used in drug development to improve the pharmacokinetics and bioavailability of drugs. It has also been investigated as a potential imaging probe for cancer diagnosis and treatment. Clinical trials have shown promising results for the use of Ald-Ald-PEG4-t-butyl ester4-t-butyl ester in cancer therapy, but further studies are needed to determine its safety and efficacy. In environmental research, Ald-Ald-PEG4-t-butyl ester4-t-butyl ester has been used to study the effects of pollutants on aquatic organisms and to develop sustainable pollution management strategies. In industrial research, Ald-Ald-PEG4-t-butyl ester4-t-butyl ester has been used to improve the efficiency and quality of various manufacturing processes, including the production of polymers, coatings, and adhesives. Health and safety considerations are crucial when using Ald-Ald-PEG4-t-butyl ester4-t-butyl ester in industrial settings, and proper protective measures should be employed to prevent exposure to hazardous chemicals.

Future Perspectives and Challenges

Despite the promising applications of Ald-Ald-PEG4-t-butyl ester4-t-butyl ester, several challenges need to be addressed to fully exploit its potential. One of the main limitations is the lack of understanding of its pharmacokinetics and toxicity in vivo. Further studies are needed to determine the optimal dose, route of administration, and target tissue for Ald-Ald-PEG4-t-butyl ester4-t-butyl ester. Another challenge is the development of more efficient and sustainable methods for its synthesis and purification. The use of renewable resources and green chemistry principles should be employed to minimize the environmental impact of Ald-Ald-PEG4-t-butyl ester4-t-butyl ester production. Future trends and prospects in the application of Ald-Ald-PEG4-t-butyl ester4-t-butyl ester in scientific research include the development of new bioconjugation strategies, the use of Ald-Ald-PEG4-t-butyl ester4-t-butyl ester in gene therapy, and the exploration of its potential in regenerative medicine.

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