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25926-16-3

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  • 2,7-Naphthalenedisulfonicacid,5-[(4,6-dichloro-1,3,5-triazin-2-yl)amino]-4-hydroxy-3-[2-(1-sulfo-2-naphthalenyl)diazenyl]-

    Cas No: 25926-16-3

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  • 2,7-Naphthalenedisulfonicacid,5-[(4,6-dichloro-1,3,5-triazin-2-yl)amino]-4-hydroxy-3-[2-(1-sulfo-2-naphthalenyl)diazenyl]-

    Cas No: 25926-16-3

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25926-16-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 25926-16-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,5,9,2 and 6 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 25926-16:
(7*2)+(6*5)+(5*9)+(4*2)+(3*6)+(2*1)+(1*6)=123
123 % 10 = 3
So 25926-16-3 is a valid CAS Registry Number.
InChI:InChI=1/C23H14Cl2N6O10S3/c24-21-27-22(25)29-23(28-21)26-15-9-12(42(33,34)35)7-11-8-16(43(36,37)38)18(19(32)17(11)15)31-30-14-6-5-10-3-1-2-4-13(10)20(14)44(39,40)41/h1-9,30H,(H,33,34,35)(H,36,37,38)(H,39,40,41)(H,26,27,28,29)/b31-18+

25926-16-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-[(4,6-dichloro-1,3,5-triazin-2-yl)amino]-4-hydroxy-3-[(1-sulpho-2-naphthyl)azo]naphthalene-2,7-disulphonic acid

1.2 Other means of identification

Product number -
Other names 5-[(4,6-dichloro-1,3,5-triazin-2-yl)amino]-4-hydroxy-3-[(1-sulpho-2-naphthyl)azo]naphthalene-2,7-disulphonic acid

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

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

More Details:25926-16-3 SDS

25926-16-3Downstream Products

25926-16-3Relevant articles and documents

Synthesis and kinetic study of a series of chloro- and m-carboxypyridium triazinyl reactive dyes

Huang, Huei-Chin,Wu, Chun-Guey

, (2021)

Five monochloro-s-triazinyl reactive dyes (MCT) and five m-carboxypyridium-s-triazinyl reactive dyes (NTR) were synthesised with the same red chromophore bearing an –NHCN, –OCH3, –CH3NSO2CH3, –N-methyl phenyl or –OH group as ‘second-leg’ substituents. A kinetic study of the hydrolysis of these dyes was conducted, and the rate constant (kobs) and half-life time values were determined. The kobs of the MCT and NTR dyes was found to follow the order –OCH3 > –CH3NSO2CH3 > –N-methyl phenyl > –NHCN > –OH, which was approximately in agreement with the values obtained for the Hammett substituent constants. Overall, the higher the electron-donating property of the substituent on meta-position to the leaving group in the triazine ring, the lower the hydrolysis rate constant.

Fiber reactive dyestuffs

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Page/Page column 20, (2010/11/24)

A fiber reactive dyestuff of the following formula (I) wherein the definition of D, R, R1, R2, X and Z have the same meaning as given in the specification. The fiber reactive dyestuff of the present invention is suitable for dyeing and printing on cellulose fiber or fiber materials containing cellulose. Dyed material with various excellent properties in dyed color can be obtained, showing especially outstanding performance in the property of wash fastness, build-up and chlorine fastness.

Bridged disazo compounds

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Example 146, (2008/06/13)

Compounds of formula (I) with the meanings of D, R1, R2, X and Y as given in claim 1 can be used as paper dyes or direct dyes or for the preparation of ink-jet inks.

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