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3081-07-0

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  • [hydroxy(dimethyl)silyl]oxy-[[hydroxy(dimethyl)silyl]oxy-dimethylsilyl]oxy-dimethylsilane

    Cas No: 3081-07-0

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3081-07-0 Usage

Uses

Octamethyl-1,7-tetrasiloxanediol can be used in the preparation of Silicone coated Celgard-2400 for the adhesion of canine platelets and leucocytes.

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

3081-07-0SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name hydroxy-[[[hydroxy(dimethyl)silyl]oxy-dimethylsilyl]oxy-dimethylsilyl]oxy-dimethylsilane

1.2 Other means of identification

Product number -
Other names 1,1,3,3,5,5,7,7-Octamethyl-tetrasiloxan-1,7-diol

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:3081-07-0 SDS

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.

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