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55080-96-1

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55080-96-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 55080-96-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,5,0,8 and 0 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 55080-96:
(7*5)+(6*5)+(5*0)+(4*8)+(3*0)+(2*9)+(1*6)=121
121 % 10 = 1
So 55080-96-1 is a valid CAS Registry Number.

55080-96-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(2-hydroxyethyl)-5-nitroisoindole-1,3-dione

1.2 Other means of identification

Product number -
Other names 2-(2-hydroxy-ethyl)-5-nitro-isoindoline-1,3-dione

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:55080-96-1 SDS

55080-96-1Relevant articles and documents

Azo dyes from aminophthalimides and aniline, tetrahydroquinoline, and benzomorpholine couplers having thiosulfate groups

-

, (2008/06/13)

Disclosed are azo dyes suitable for coloring polyamide material, particularly nylon carpet and which are prepared from aminophthalimides and couplers which are STR1 substituted with a thiosulfate ester group. These dyes produce yellow to blue shades and also color cellulose acetate fabrics and wool. The dyes have the general formula: STR2 wherein R2 and R4 are each selected from hydrogen and a large variety of organic substituents, the coupler C is an aniline, 1,2,3,4-tetrahydroquinoline, or benzomorpholine derivative wherein a Q-SSO3 M group is attached to the nitrogen thereof, Q being a lower alkylene or similar linking group, and M is Na+, K+, NH4+, or H+. The present dyes are superior in such properties as fastness to light, oxides of nitrogen, wash, ozone, sublimation, perspiration and crock, and exhibit good dyeability including migration, leveling, pH stability, and build.

Phthalimidyl-azo-tetrahydro-quinoline compounds

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, (2008/06/13)

Monoazo compounds containing a phthalimidyl diazo component the aromatic ring of which can be substituted with one or two substituents, and the nitrogen of which may be substituted, and a 1,2,3,4-tetrahydroquinoline disperse azo dye coupling component which contains at least one alkyl substituent, are useful for dyeing cellulose acetate, nylon, and especially polyester fibers on which the compounds exhibit good fastness and dyeability properties.

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