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O-(2-Carboxyethyl)polyethylene glycol 3,400, also known as O-(2-CEG)-PEG 3,400, is a synthetic polymer with a molecular weight of 3,400 daltons. It is composed of a polyethylene glycol (PEG) backbone with a carboxyethyl group attached to one end. This unique structure endows O-(2-CEG)-PEG 3,400 with versatile properties, making it a valuable building block in various applications across different industries.

117786-94-4

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117786-94-4 Usage

Uses

Used in Pharmaceutical Industry:
O-(2-Carboxyethyl)polyethylene glycol 3,400 is used as a reactant for the preparation of multifunctional polymeric micelles for antiviral treatment. The carboxyethyl group allows for the attachment of antiviral agents, enhancing their solubility, stability, and targeted delivery to infected cells.
Used in Cancer Therapy:
O-(2-Carboxyethyl)polyethylene glycol 3,400 is used as a reactant for the preparation of NO-PEGylated epirubicin, a chemotherapy agent. The PEGylation of epirubicin with O-(2-CEG)-PEG 3,400 improves the drug's pharmacokinetics, reduces side effects, and enhances its therapeutic efficacy against cancer cells.
Used in Biomaterials and Surface Modification:
O-(2-Carboxyethyl)polyethylene glycol 3,400 is used as a reactant for the preparation of functionalized oligomers and copolymers with terpyridine-metal complexing segments. These functionalized polymers can be used to modify the surface properties of biomaterials, such as increasing the sensitivity of carboxyl-terminated dendrimer-coated bioactive interfaces for protein microarrays.
Used in Cardiovascular Research:
O-(2-Carboxyethyl)polyethylene glycol 3,400 is used in studies of therapeutic usefulness for receptor-targeted blockage of oxidized low-density lipoprotein uptake. The carboxyethyl group can be used to conjugate targeting ligands, enabling the development of targeted therapies for atherosclerosis and other cardiovascular diseases.

Check Digit Verification of cas no

The CAS Registry Mumber 117786-94-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,7,7,8 and 6 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 117786-94:
(8*1)+(7*1)+(6*7)+(5*7)+(4*8)+(3*6)+(2*9)+(1*4)=164
164 % 10 = 4
So 117786-94-4 is a valid CAS Registry Number.

117786-94-4SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name O-(2-Carboxyethyl)polyethylene glycol

1.2 Other means of identification

Product number -
Other names Polyethylene glycol 3400 monoacid

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:117786-94-4 SDS

117786-94-4Downstream Products

117786-94-4Relevant academic research and scientific papers

PHTHALOCYANINE DYE COMPOUNDS, CONJUGATES AND METHODS OF USE THEREOF

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Paragraph 000138-000139; 000198-000199, (2021/10/15)

Disclosed herein are phthalocyanine dyes, and conjugates thereof, useful as fluorescent reporters for bioassays, for optical imaging and as therapeutic conjugates as the photosensitizing agents in light-based therapies including photoimmuno therapy (PIT). Certain phthalocyanine dyes disclosed herein are water soluble, and possess photophysical and photochemical profiles useful for use in imaging or therapy.

NOVEL CONJUGATES, PREPARATION THEREOF, AND THERAPEUTIC USE THEREOF

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, (2012/09/11)

Provided herein are cryptophycin conjugates and compositions containing them. Methods of making and using such compounds also are provided

Novel 3-O-pegylated carboxylate and 3-O-pegylated carbamate prodrugs of naltrexone for microneedle-enhanced transdermal delivery

Yerramreddy, Thirupathi Reddy,Milewski, Mikolaj,Penthala, Narsimha Reddy,Stinchcomb, Audra L.,Crooks, Peter A.

scheme or table, p. 3280 - 3283 (2010/08/19)

A small library of novel 3-O-pegylated carboxylate prodrugs (4a-4b) and 3-O-pegylated carbamate prodrugs (9a-9b) of naltrexone were synthesized. The goal behind the design of these prodrugs was to investigate their potential for microneedle-enhanced transdermal delivery. All the synthesized 3-O-pegylated carboxylate prodrugs (4a-4b) and 3-O-pegylated carbamate prodrugs (9a-9b) of naltrexone were found to have adequate stability in a transdermal formulation and improved apparent solubility compared to naltrexone. Viscosity effects were postulated to be responsible for the observed non-linearity in the flux-concentration profile of these prodrugs.

3-Fucosyl-N-acetyl lactosamine derivatives, and their biological applications

-

, (2008/06/13)

The invention relates to substitution derivatives of trisaccharide 3-fucosyl-N-acetyl lactosamine and to the immunological applications of these derivatives and of the trisaccharide itself particularly as diagnostic reagent and in therapy.

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