What is the Tetraethylene Glycol Mono-2-methylallyl Ether?

Tetraethylene Glycol Mono-2-methylallyl Ether is , while it's Molecular Formula is C 12 H 24 O 5 . Used in Pharmaceutical Industry: Tetraethylene Glycol Mono-2-methylallyl Ether is used as a drug delivery agent for enhancing the solubility, stability, and bioavailability of therapeutic compounds. Its hydrophilic nature allows for improved interaction with biological systems, facilitating the delivery of drugs to target sites. Used in Tissue Engineering: In the field of tissue engineering, Tetraethylene Glycol Mono-2-methylallyl Ether is used as a component in the development of scaffolds and hydrogels. Its flexibility and hydrophilicity contribute to the creation of structures that can support cell growth and tissue regeneration. Used in Other Biological Applications: Tetraethylene Glycol Mono-2-methylallyl Ether is also utilized in various other biological applications, such as in the development of biosensors, diagnostic tools, and lab-on-a-chip devices. Its unique properties enable the creation of innovative solutions for a wide range of biological and medical challenges.

What is the CAS number for Tetraethylene Glycol Mono-2-methylallyl Ether?

The CAS number of Tetraethylene Glycol Mono-2-methylallyl Ether is 31497-33-3.

What is Tetraethylene Glycol Mono-2-methylallyl Ether (31497-33-3) used for?

Tetraethylene Glycol Mono-2-methylallyl Ether is a hydrophilic polymer derived from poly(ethylene glycol) methyl ether (mPEG). It is characterized by its ability to control the flexibility of a composite material and possesses properties that make it suitable for a range of applications in various industries.

What is the Tetraethylene Glycol Mono-2-methylallyl Ether?

Tetraethylene Glycol Mono-2-methylallyl Ether is , while it's Molecular Formula is C 12 H 24 O 5 . Used in Pharmaceutical Industry: Tetraethylene Glycol Mono-2-methylallyl Ether is used as a drug delivery agent for enhancing the solubility, stability, and bioavailability of therapeutic compounds. Its hydrophilic nature allows for improved interaction with biological systems, facilitating the delivery of drugs to target sites. Used in Tissue Engineering: In the field of tissue engineering, Tetraethylene Glycol Mono-2-methylallyl Ether is used as a component in the development of scaffolds and hydrogels. Its flexibility and hydrophilicity contribute to the creation of structures that can support cell growth and tissue regeneration. Used in Other Biological Applications: Tetraethylene Glycol Mono-2-methylallyl Ether is also utilized in various other biological applications, such as in the development of biosensors, diagnostic tools, and lab-on-a-chip devices. Its unique properties enable the creation of innovative solutions for a wide range of biological and medical challenges.

What is the CAS number for Tetraethylene Glycol Mono-2-methylallyl Ether?

The CAS number of Tetraethylene Glycol Mono-2-methylallyl Ether is 31497-33-3.

What is Tetraethylene Glycol Mono-2-methylallyl Ether (31497-33-3) used for?

Tetraethylene Glycol Mono-2-methylallyl Ether is a hydrophilic polymer derived from poly(ethylene glycol) methyl ether (mPEG). It is characterized by its ability to control the flexibility of a composite material and possesses properties that make it suitable for a range of applications in various industries.

Product classification

31497-33-3

Product Name：Polyethylene glycol monomethallyl ether
Molecular Formula：
Purity：99%
Molecular Weight：248.32

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Product Details;

CasNo： 31497-33-3

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Molecular Formula:C₁₂H₂₄O₅
Molecular Weight:248.32

31497-33-3 Relevant articles

Intramolecular Bromoalkoxylation: Synthesis of 2-Bromomethyl-2-methyl Crown Ethers

Nakamura, Tetsuya,Nakatsuji, Yohji,Okahara, Mitsuo

, p. 219 (1981)

2-Bromomethyl-2-methyl crown ethers were...

PRODUCTION METHOD OF UNSATURATED (POLY)ALKYLENE GLYCOL ETHER MONOMER AND PRODUCTION METHOD OF (POLY)ALKYLENE GLYCOL CHAIN-CONTAINING POLYMER

-

Page/Page column 37, (2010/06/14)

To provide a production method of a (pol...

Structural control of the monolayer stability of water-soluble gold nanoparticles

Agasti, Sarit S.,You, Chang-Cheng,Arumugam, Palaniappan,Rotello, Vincent M.

, p. 70 - 73 (2008/12/20)

The thermodynamic and kinetic stability ...

Molecular Design of the Electron-Donating Sidearm of Lariat Ethers: Effective Coordination of the Quinoline Moiety in Complexation toward Alcali-Metal Cations

Nakatsuji, Yohji,Nakamura, Tetsuya,Yonetani, Masayuki,Yuya, Hajime,Okahara, Mitsuo

, p. 531 - 538 (2007/10/02)

The electron-donating sidearm of alkyl-s...

Regio- and Stereoselectivity of the Intramolecular C-H Insertion by Cyclopropylidenes Bearing a Remote Oxido Substituent

Harada, Toshiro,Yamaura, Yasunari,Oku, Akira

, p. 1715 - 1720 (2007/10/02)

(ω-Oxidoalkyl)cyclopropylidenes generate...

31497-33-3 Process route

: 107-21-1
ethylene glycol

: 563-47-3
3-Chloro-2-methylpropene

: 5175-48-4,31497-33-3
2-(2-methylallyloxy)ethanol

: 50975-38-7
ethylene glycol bis(2-methylallyl) ether

Conditions

Conditions	Yield
With water; sodium hydroxide; at 60 - 70 ℃; for 6h; Industry scale;	80.2% 11.8%

: 563-47-3
3-Chloro-2-methylpropene

: 112-27-6
2,2'-[1,2-ethanediylbis(oxy)]bisethanol

: 111719-00-7,31497-33-3
triethylene glycol mono-2-methylallyl ether