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2-amino-4-[(4,6-dichloro-1,3,5-triazin-2-yl)amino]benzenesulfonic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

15935-11-2

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15935-11-2 Usage

Chemical structure

Contains a benzene ring with two amino groups and two chloro groups, as well as a triazine ring with an amino group attached

Use

Sulfonic acid used in the production of dyes, pigments, and other chemical applications

Applications

Used as a reactive dye intermediate and in the synthesis of fluorescent dyes

Potential industrial applications

Water treatment, reactive intermediate in organic synthesis

Check Digit Verification of cas no

The CAS Registry Mumber 15935-11-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,9,3 and 5 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 15935-11:
(7*1)+(6*5)+(5*9)+(4*3)+(3*5)+(2*1)+(1*1)=112
112 % 10 = 2
So 15935-11-2 is a valid CAS Registry Number.

15935-11-2SDS

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 3-dichloro-s-triazinylaminoaniline-6-sulphonic acid

1.2 Other means of identification

Product number -
Other names -

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:15935-11-2 SDS

15935-11-2Relevant academic research and scientific papers

Synthesis and antibacterial activity of some novel nucleus N-aminorhodanine based bis monofunctional and bifunctional reactive dyes and their application on wool and cotton fabrics

Mohamed, Fatma A.,Shaban, Elkhabiry,Ibrahim, Hassan M.

, p. 597 - 608 (2022/01/08)

Herein, we aimed to synthesis two new reactive dyes based on derivatives of Aminorodanine as a chromoforic group, as well as to apply the dye and antibacterial activity to the dyed fabric. First, we synthesized 3-amino rhodanine with glutaraldehyde and te

Multi-active-group red dye with high fixation rate and high chlorine fastness for printing and preparation method thereof

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Paragraph 0033; 0040; 0047-0048, (2021/04/21)

The invention discloses a multi-active-group red dye with high fixation rate and high chlorine fastness for printing and a preparation method thereof, the multi-active-group red dye comprises a compound as shown in a structural general formula I, in the s

Synthesis and application of novel reactive dyes based on dimedone moiety

Mohamed, Fatma A.,Abd El-Megied, Saadia A.,Mohareb, Rafat M.

, p. 4447 - 4455 (2020/12/11)

The aim of this study is synthesising, characterizing and finding out properties of some new bifunctional dye Bis (monochlorotriazine) (MCT) and heterobifunctional (monochlorotriazine / sulphatoethylsulphone) (MCT/SES) reactive dyes using Dimedone moiety

Yellow-orange reactive dye and method thereof in dying cotton fiber in non-aqueous media

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Paragraph 0039-0043, (2019/06/07)

The invention relates to a compound containing multiple sulfonic acid groups and application of the compound. The compound is a compound shown in the formula I or salt of the compound (definitions ofR1-R5 are shown in the specification or claims). The com

High-light-fastness emerald reactive dye compound and application thereof

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Paragraph 00223; 0026, (2018/03/24)

The invention provides a high-light-fastness emerald reactive dye compound, which has the following general structural formula (I), a+b+c=3.5, wherein CuPc, X, R1, R2 and R3 are as defined in the specification. The high-light-fastness emerald reactive dye

High-light-fastness emerald pyridone reactive dye compound and preparation method and application thereof

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Paragraph 0048; 0049; 0051, (2018/03/24)

The invention discloses a high-light-fastness emerald pyridone reactive dye compound and a preparation method and application thereof. The dye compound has the following general structural formula (I), a+b+c=3.5, wherein CuPc, M, n, X, R1, R2, R3, R4, R5,

Printing and dyeing physiognomies of synthesized Azo-multifunctional reactive dyes using exhaust technique

Saeed,Bhatti,Zuber,Bhatti,Zia

, p. 2473 - 2476 (2015/12/11)

Four poly-functional reactive dyes keeping mono or bis reactive group have been synthesized and applied successfully to cotton fabric. The main target of study was to synthesize novel reactive dyes having multiple reactive cites to show maximum colour str

Studies on application and fastness properties of multifunctional reactive dyes on cotton

Saeed, Qurat-Ul-Ain,Bhatti, Ijaz Ahmad,Abbas, Muhammad

, p. 666 - 672 (2013/07/26)

Reactive dyes are extensively used for dyeing of cotton but the problem associated with them is the removal of most of the dye from the fabrics during washing. In order to improve fixation of dye on fabric a series of H- acid based mono and bisazo reactiv

Novel reactive dyestuff with N-alkylamino group

-

Page/Page column 6, (2011/02/18)

The present invention relates to a novel reactive dyestuff with a N-alkylamino group, represented by the following formula (I): wherein A1, A2, R1, R2, R3, R4, (R5)0-2

Reactive dyes containing an alkylthio-s-triazinyl reactive group

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Page/Page column 10; 18, (2008/06/13)

A reactive dyestuff containing an alkylthio-s-triazinyl reactive group of the following formula (I) is disclosed, wherein A, X, Y, Z, R, Q, and a are defined the same as the specification. It is suitable for exhaust dyeing, cold batch-up dyeing and contin

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