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75888-21-0

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75888-21-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 75888-21-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,5,8,8 and 8 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 75888-21:
(7*7)+(6*5)+(5*8)+(4*8)+(3*8)+(2*2)+(1*1)=180
180 % 10 = 0
So 75888-21-0 is a valid CAS Registry Number.
InChI:InChI=1/C18H39NO6/c1-4-20-13-16-23-10-7-19(8-11-24-17-14-21-5-2)9-12-25-18-15-22-6-3/h4-18H2,1-3H3

75888-21-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(2-ethoxyethoxy)-N,N-bis[2-(2-ethoxyethoxy)ethyl]ethanamine

1.2 Other means of identification

Product number -
Other names EINECS 278-335-9

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:75888-21-0 SDS

75888-21-0Relevant articles and documents

Process for the disproportionation of silanes

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, (2008/06/13)

Silane, SiH4, and diochlorosilane, particularly suitable for the preparation of silicon are readily obtained by disproportionating trichlorosilane to dichlorosilane and, ultimately silane by reacting: (a) a silane containing at least one Si-H bond, of the general formula Rn Hm SiX4-(n+m) wherein R represents an alkyl or aryl group, x represents a halogen or an alkoxy group, n is an integer equal to 0, 1, 2 or 3 and m is an integer equal to 1, 2 or 3, and (b) a catalyst system comprising an ionic inorganic salt of the formula M+ A- and a compound capable of at least partially dissociating the salt by complexing its cation M+.

Process for the preparation of tris-(ether-amines) and the tris-(ether-amines) produced

-

, (2008/06/13)

A process of preparing tris-(ether-amines) of the formula: in which R represents a hydrocarbon radical, A and B represent alkanediyl radicals, and n is a whole number between zero and 4, by ammonolysis of an alkylene glycol mono-ether of the formula: in the presence of 10 to 40 percent by weight of a hydrogenation-dehydrogenation catalyst, based on weight of said alkylene glycol monoether. The tris-(ether-amines) produced, such as tris-(3,6-dioxa-octyl)amine, tris-(3,6,9-trioxaundecyl)amine, tris-(3,6-dioxaheptyl)amine, and tris-(3,6-dioxadecyl)amine.

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