20387-39-7 Usage
Description
1,1'-(Hexamethylenedioxy)bis(3-chloropropan-2-ol) is a diol chemical compound with the molecular formula C10H20Cl2O4. It features two hydroxyl groups and a chlorine atom attached to a hexamethylene-bridged ether moiety, which contributes to its versatile applications in various industries.
Uses
Used in Polymer and Resin Synthesis:
1,1'-(Hexamethylenedioxy)bis(3-chloropropan-2-ol) is used as a precursor in the chemical industry for the synthesis of various polymers and resins. Its unique structure allows it to serve as a building block for creating complex polymeric materials with specific properties.
Used in Plastics and Rubber Production:
In the plastics and rubber industry, 1,1'-(Hexamethylenedioxy)bis(3-chloropropan-2-ol) is utilized as a crosslinking agent. This role enhances the mechanical properties and durability of the final products by forming covalent bonds between polymer chains, leading to improved structural integrity and performance.
Used in Disinfectants and Preservatives:
Due to its antimicrobial properties, 1,1'-(Hexamethylenedioxy)bis(3-chloropropan-2-ol) is employed in the formulation of disinfectants and preservatives. It helps to inhibit the growth of microorganisms, making it a valuable component in products designed to maintain cleanliness and prevent spoilage.
Safety Precautions:
It is crucial to handle 1,1'-(Hexamethylenedioxy)bis(3-chloropropan-2-ol) with care, as it can be hazardous if not properly managed. Adequate safety measures should be taken during its storage, transportation, and use to minimize potential risks to human health and the environment.
Check Digit Verification of cas no
The CAS Registry Mumber 20387-39-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,3,8 and 7 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 20387-39:
(7*2)+(6*0)+(5*3)+(4*8)+(3*7)+(2*3)+(1*9)=97
97 % 10 = 7
So 20387-39-7 is a valid CAS Registry Number.
20387-39-7Relevant articles and documents
Synthesis of [14C]-Labelled glycidyl and glycerol ethers of aliphatic and aromatic alcohols.
Van Elburg,Ormskerk,De Kloe,Boogaard
, p. 147 - 167 (2007/10/03)
The synthesis of [14C]-labelled glycidyl ethers and the corresponding glycerol ethers is described for the monofunctional compounds 1-dodecanol and ortho-cresol and the bifunctional compounds 4,4'-dihydroxy-3,3',5,5'-tetramethyl biphenyl and 1,6-hexanediol. The synthesis is based on reaction between the alcohol and [U-14C]-epichlorohydrin. The aromatic compounds have been converted to the corresponding glycidyl ethers by using sodium hydroxide and the aliphatic compounds by using tin(IV) chloride as a catalyst. Thus radio-labelled glycidyl ethers were obtained in yields between 50-80, with a chemical purity of > 92 and a radiochemical purity of > 95 by HPLC. The specific activities of the glycidyl ethers were approximately 0.2 mCi/mmol for the monofunctional compounds and approximately 0.4 mCi/mmol for the bifunctional compounds.