3081-07-0 Usage
Description
1,7-Tetrasiloxanediol, 1,1,3,3,5,5,7,7-octamethylis a chemical compound characterized by its unique structure and properties. It is a type of siloxane molecule with a central diol group and eight methyl groups attached to the silicon atoms. 1,7-Tetrasiloxanediol, 1,1,3,3,5,5,7,7-octamethylis known for its stability, low reactivity, and ability to form stable coatings or films.
Uses
Used in Medical Applications:
1,7-Tetrasiloxanediol, 1,1,3,3,5,5,7,7-octamethylis used as a coating material for [Celgard-2400], a type of microporous membrane, to enhance the adhesion of canine platelets and leucocytes. This application is particularly relevant in the field of medical research and development, where understanding the interaction between blood cells and various surfaces is crucial for the design of medical devices and implants.
In this specific application, the compound is used to create a silicone-coated Celgard-2400 membrane, which is then tested for its ability to promote the adhesion of canine platelets and leucocytes. This can be useful in the development of artificial organs, blood-contacting devices, and other medical applications where the interaction between blood cells and the device material is a critical factor.
Check Digit Verification of cas no
The CAS Registry Mumber 3081-07-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,0,8 and 1 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 3081-07:
(6*3)+(5*0)+(4*8)+(3*1)+(2*0)+(1*7)=60
60 % 10 = 0
So 3081-07-0 is a valid CAS Registry Number.
InChI:InChI=1/C8H26O5Si4/c1-14(2,9)11-16(5,6)13-17(7,8)12-15(3,4)10/h9-10H,1-8H3
3081-07-0Relevant articles and documents
Rate studies of the acid-catalyzed solvolysis of eight-membered cyclosilazoxanes
Lasocki, Zygmunt,Witekowa, Malgorzata
, p. 27 - 33 (2007/10/02)
The solvolysis of N-phenyl-1,1,3,3,5,5,7,7-octamethyl-1,3,5,7-tetrasila-2-aza-4,6,8-trioxacyclooctane (1) and N,N'-diphenyl-1,1,3,3,5,5,7,7-octamethyl-1,3,5,7-tetrasila-2,6-diaza-4,8-dioxacyclooctane (II) in methanol/water in the presence of an acetate buffer is a pseudo-first-order process, subject to general acid-catalysis.The catalytic rate constants have been determined spectrophotometrically for the solvolysis of I.The ring cleavage is slower than that of analogous six-membered cyclosilazoxanes, but the catalytic mode and the solvent isotope effect indicate a close mechanistic similarity between the solvolyses of six- and eight-membered rings.
