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2,2'-[(4,6-dichloro-1,3,5-triazin-2-yl)imino]bisethanol, commonly known as Disperse Blue 106, is a synthetic organic compound characterized by a 1,3,5-triazine ring and two hydroxyethyl groups. It is renowned for its vibrant blue color and is widely recognized in the textile industry as a dye for polyester and acetate fibers. Additionally, it finds applications in the production of colored plastics and inks.

13436-79-8

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13436-79-8 Usage

Uses

Used in Textile Industry:
2,2'-[(4,6-dichloro-1,3,5-triazin-2-yl)imino]bisethanol is used as a dye for coloring polyester and acetate fibers, providing them with a rich and vibrant blue hue. Its affinity for these synthetic fibers makes it a popular choice in the textile manufacturing process.
Used in Plastics Industry:
In the plastics industry, 2,2'-[(4,6-dichloro-1,3,5-triazin-2-yl)imino]bisethanol is used as a colorant to produce various shades of blue in plastic materials, enhancing the visual appeal and customization options for plastic products.
Used in Ink Production:
2,2'-[(4,6-dichloro-1,3,5-triazin-2-yl)imino]bisethanol is utilized as a pigment in the formulation of inks, particularly for printing applications that require a deep and consistent blue color.
Safety Considerations:
While Disperse Blue 106 is considered to be relatively low in toxicity, it is essential to handle the compound with proper safety measures during its production and application. This includes minimizing exposure to human health and the environment to ensure responsible use and mitigate any potential risks.

Check Digit Verification of cas no

The CAS Registry Mumber 13436-79-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,4,3 and 6 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 13436-79:
(7*1)+(6*3)+(5*4)+(4*3)+(3*6)+(2*7)+(1*9)=98
98 % 10 = 8
So 13436-79-8 is a valid CAS Registry Number.

13436-79-8SDS

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-[(4,6-dichloro-1,3,5-triazin-2-yl)-(2-hydroxyethyl)amino]ethanol

1.2 Other means of identification

Product number -
Other names 2,2'-[(4,6-dichloro-1,3,5-triazin-2-yl)imino]diethanol

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:13436-79-8 SDS

13436-79-8Relevant academic research and scientific papers

BONDING METHOD, BONDABILITY IMPROVING AGENT, SURFACE MODIFICATION METHOD, SURFACE MODIFYING AGENT, AND NOVEL COMPOUND

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Paragraph 0350-0355, (2016/06/28)

To provide a technique by which an —OH group can be effectively formed on a material surface for the purpose of making the material suitable for bonding (for example, for molecular bonding) that utilizes a chemical reaction (chemical binding). [Solution] A bonding method for bonding a substrate A and a substrate B, which comprises: a step for applying an agent that contains the compound (α) described below on the surface of the substrate A; a step for arranging the substrate B so as to face the compound (α) that is present on the surface of the substrate A; and a step for integrally bonding the substrate A and the substrate B by applying a force onto the substrate A and/or the substrate B. The compound (α) is a compound that has an OH group or an OH-forming group, an azide group and a triazine ring in each molecule, and the substrate A is configured using a polymer.

New penicillin derivatives

Adure, A. S.,Shelar, A. R.

, p. 759 - 760 (2007/10/02)

New penicillin derivatives have been synthesized by condensation of mono-substituted cyanuric chlorides (3) with 6-aminopenicillanic acid (2), and screened for their antibacterial activity against S. aureus, E. coli, K. pneumonae, S. typhi and P. aeruginosa at 500 μg/ml concentration.Compounds 4a and 4d are inactive while compound 4c is active against all the tested micro-organisms.

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