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118377-62-1

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  • 1H-Pyrrole-2,5-dione,1,1'-[(1-methylethylidene)bis(oxy-2,1-ethanediyl)]bis-

    Cas No: 118377-62-1

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  • Organix Inc.
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118377-62-1 Usage

Chemical structure

A central propane molecule with two maleimide groups attached at both ends.

Functionality

Bifunctional reagent.

Reactivity

High reactivity with thiol-containing molecules.

Bond formation

Capable of forming stable covalent bonds.

Applications

Production of polymer materials, adhesives, coatings, and biomedical applications.

Solubility

Good solubility in organic solvents.

Stability

Stable under a wide range of conditions.

Importance

A key compound for the development of new materials and technologies.

Handling

Requires careful handling and understanding of potential health and environmental hazards.

Check Digit Verification of cas no

The CAS Registry Mumber 118377-62-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,8,3,7 and 7 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 118377-62:
(8*1)+(7*1)+(6*8)+(5*3)+(4*7)+(3*7)+(2*6)+(1*2)=141
141 % 10 = 1
So 118377-62-1 is a valid CAS Registry Number.
InChI:InChI=1/C15H18N2O6/c1-15(2,22-9-7-16-11(18)3-4-12(16)19)23-10-8-17-13(20)5-6-14(17)21/h3-6H,7-10H2,1-2H3

118377-62-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-[2-[2-[2-(2,5-dioxopyrrol-1-yl)ethoxy]propan-2-yloxy]ethyl]pyrrole-2,5-dione

1.2 Other means of identification

Product number -
Other names BMEP

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:118377-62-1 SDS

118377-62-1Downstream Products

118377-62-1Relevant articles and documents

Dendrimeric alkylated polyethylenimine nano-carriers with acid-cleavable outer cationic shells mediate improved transfection efficiency without increasing toxicity

Steele, Terry W. J.,Shier, Wayne Thomas

, p. 683 - 698 (2010)

Purpose. Improved polycation-based non-viral DNA vectors were sought by preparing dendrimers with polyethylenimine cores surrounded by various shells incorporating structural features intended to facilitate steps in transfection mechanisms. Dendrimeric vectors were designed with (a) an outer oligocation shell, intended to facilitate DNA release inside cells, (b) a hydrophobic C-16 alkyl shell, and (c) a polycationic core, the latter two intended to combine lipid-depletion and osmotic burst endosome escape mechanisms, respectively, and were (d) attached through an a acid-cleavable linker reported to hydrolyze at endosomal pH values. Methods. Vectors and DNA complexes were characterized by dynamic and static light scattering. Flow cytometry was used to quantitate transfection activity and cytotoxicity in CHO-Kl cells. Results. About 5-fold increased transfection activity was obtained for a vector constructed with an outer shell of oligocations attached through acid-cleavable linkers, relative to a control dendrimer with an acidstable linker. The most effective oligocation component of outer shells tested was spermine. Neither modification was associated with increased cytotoxicity. This vector design did not permit an evaluation of the benefit of combining endosome release mechanisms. Conclusion. Using acid-cleavable linkers to attach an outer shell of short, highly-charged oligocations to a PEI-based dendrimeric vector substantially increased transfection efficiency without increasing cytotoxicity.

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