3610-27-3 Usage
Uses
Used in the Textile Industry:
2[2(2-METHOXYETHOXY)ETHOXY]ETHANOL ACETATE is used as an antidusting agent for finely powdered materials, such as dyestuffs, to prevent the formation of dust clouds and improve the working environment.
Used in the Chemical Industry:
2[2(2-METHOXYETHOXY)ETHOXY]ETHANOL ACETATE is used as a solvent in various chemical processes due to its water solubility and low volatility, making it suitable for a range of applications in the chemical industry.
Used in the Cosmetics Industry:
2[2(2-METHOXYETHOXY)ETHOXY]ETHANOL ACETATE is used as an ingredient in the formulation of cosmetics and personal care products, taking advantage of its water solubility and fruity odor to enhance the product's sensory properties.
Used in the Pharmaceutical Industry:
2[2(2-METHOXYETHOXY)ETHOXY]ETHANOL ACETATE can be used as a solvent or excipient in the pharmaceutical industry for the development of various drug formulations, leveraging its chemical properties to improve drug delivery and stability.
Safety Profile
Mildly toxic by ingestion and skincontact. An eye irritant. Combustible. Tofight fire, use alcohol foam, CO2, dry chemical. Whenheated to decomposition it emits acrid smoke and irritatingfumes.
Check Digit Verification of cas no
The CAS Registry Mumber 3610-27-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,6,1 and 0 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 3610-27:
(6*3)+(5*6)+(4*1)+(3*0)+(2*2)+(1*7)=63
63 % 10 = 3
So 3610-27-3 is a valid CAS Registry Number.
InChI:InChI=1/C9H18O5/c1-3-14-9(10)8-13-7-6-12-5-4-11-2/h3-8H2,1-2H3
3610-27-3Relevant academic research and scientific papers
Heterobimetallic dinuclear lanthanide alkoxide complexes as acid-base difunctional catalysts for transesterification
Zeng, Ruijie,Sheng, Hongting,Zhang, Yongcang,Feng, Yan,Chen, Zhi,Wang, Junfeng,Chen, Man,Zhu, Manzhou,Guo, Qingxiang
, p. 9246 - 9252 (2014/12/11)
A practical lanthanide(III)-catalyzed transesterification of carboxylic esters, weakly reactive carbonates, and much less-reactive ethyl silicate with primary and secondary alcohols was developed. Heterobimetallic dinuclear lanthanide alkoxide complexes [Ln2Na8{(OCH2CH2NMe2)}12(OH)2] (Ln = Nd (I), Sm (II), and Yb (III)) were used as highly active catalysts for this reaction. The mild reaction conditions enabled the transesterification of various substrates to proceed in good to high yield. Efficient activation of transesterification may be endowed by the above complexes as cooperative acid-base difunctional catalysts, which is proposed to be responsible for the higher reactivity in comparison with simple acid/base catalysts.
FLUOROCHEMICAL TREATMENT FOR SILICON ARTICLES
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Page 21-22, (2010/02/05)
Silicon substrates having Si-H bonds are chemically modified using a fluorinated olefin having the formula wherein m is an integer greater than or equal to 1; n is an integer greater than or equal to 0; Z is a divalent linking group; and Rf is a highly fluorinated organic group.
