4039-63-8 Usage
Description
1-(2-isopropoxy-1-methylethoxy)propan-2-ol, also known as Di(ethylene glycol) isopropyl ether or Arcosolv PM, is a chemical compound with the molecular formula C10H22O3. It is a clear, colorless liquid that exhibits a mild, fruity odor and is soluble in water. This versatile compound is widely utilized in various industries due to its unique properties.
Uses
Used in the Coatings Industry:
1-(2-isopropoxy-1-methylethoxy)propan-2-ol is used as a solvent for the production of coatings, facilitating the application process and improving the final product's quality. Its solubility in water and mild odor make it a preferred choice for this application.
Used in the Adhesives Industry:
In the adhesives industry, 1-(2-isopropoxy-1-methylethoxy)propan-2-ol is used as a solvent to enhance the adhesive's bonding properties and workability. Its ability to dissolve various components contributes to the creation of effective and long-lasting adhesives.
Used in the Cleaning Products Industry:
1-(2-isopropoxy-1-methylethoxy)propan-2-ol is employed as a solvent in the formulation of cleaning products, aiding in the effective removal of dirt and stains. Its solubility properties allow for the even distribution of cleaning agents, ensuring thorough cleaning results.
Used in the Pharmaceutical Industry:
This chemical is used as a solvent in the synthesis of pharmaceuticals, playing a crucial role in the development of various medications. Its compatibility with a range of substances makes it a valuable component in the production of drugs.
Used in the Agrochemicals Industry:
1-(2-isopropoxy-1-methylethoxy)propan-2-ol is utilized as a solvent in the production of agrochemicals, such as pesticides and fertilizers. Its ability to dissolve active ingredients and improve the overall effectiveness of these products contributes to its widespread use in this industry.
Used in the Fragrance Industry:
In the fragrance industry, 1-(2-isopropoxy-1-methylethoxy)propan-2-ol is used as an ingredient in personal care products and perfumes, thanks to its mild, fruity odor. Its pleasant scent and solubility properties make it an ideal choice for enhancing the fragrance of various products.
Used in the Personal Care Products Industry:
1-(2-isopropoxy-1-methylethoxy)propan-2-ol is also used in the formulation of personal care products, such as lotions, creams, and shampoos, for its fragrance-enhancing properties. Its mild odor and compatibility with other ingredients make it a popular choice for improving the sensory experience of these products.
Check Digit Verification of cas no
The CAS Registry Mumber 4039-63-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,0,3 and 9 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 4039-63:
(6*4)+(5*0)+(4*3)+(3*9)+(2*6)+(1*3)=78
78 % 10 = 8
So 4039-63-8 is a valid CAS Registry Number.
InChI:InChI=1/C9H20O3/c1-7(2)11-6-9(4)12-5-8(3)10/h7-10H,5-6H2,1-4H3
4039-63-8Relevant articles and documents
13C-N.M.R.-SPECTRAL AND RELATED STUDIES ON THE DISTRIBUTION OF SUBSTITUENTS IN O-(2-HYDROXYPROPYL)CELLULOSE
Lee, Dae-Sil,Perlin, Arthur S.
, p. 1 - 20 (2007/10/02)
Information about the degree of substitution at individual oxygen atoms of O-(2-hydroxypropyl)cellulose, and the total molar substitution, was obtained from 13C-n.m.r. spectra of the intact polymer and of its hydrolyzate.On the basis of their 13-CH3 chemical-shifts, O-(2-hydroxypropyl) (HOPr) substituents occurring singly, or as terminal units of substituent chains, were radily distinguished from inner HOPr units of chains.Differentiation between monomeric HOPr units and longer chains located at O-2 of D-glucosyl residues was effected by the transformation of appropriatly substituted sugars in the hydrolyzate into 1,2-cyclic acetals incorporating a 2-O-(2-hydroxypropyl) group.Similarly, the pattern of substitution at O-6 of D-glucosyl residues was determined, through selective degradation, from the identity of HOPr derivatives of ethylene glycol, representing C-5 and C-6 of the residues.Overall, it was found that, although O-2 and O-6 are more readily substituted than O-3, the rate at which each, initially introduced, HOPr substituent is converted into a dimeric structure is not materially affected by its location.Also described are the synthesis and the n.m.r. spectra of several HOPr derivatives of D-glucose, and of simple alkanols that served as model compounds.
