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2,2'-[[4-[(2,6-dichloro-4-nitrophenyl)azo]phenyl]imino]bisethanol, commonly known as Tartrazine, is a synthetic azo dye characterized by its bright yellow color. It is widely recognized for its use as a colorant in various industries due to its vibrant hue and synthetic origin, which allows for consistent color reproduction. Despite ongoing debates regarding its safety, Tartrazine remains a prevalent choice for coloring applications.

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  • 2-[[4-(2,6-dichloro-4-nitro-phenyl)diazenylphenyl]-(2-hydroxyethyl)amino]ethanol

    Cas No: 63467-07-2

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  • 2-[[4-(2,6-dichloro-4-nitro-phenyl)diazenylphenyl]-(2-hydroxyethyl)amino]ethanol

    Cas No: 63467-07-2

  • USD $ 1.0-1.0 / Metric Ton

  • 1 Metric Ton

  • 100 Metric Ton/Day

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  • 63467-07-2 Structure
  • Basic information

    1. Product Name: 2,2'-[[4-[(2,6-dichloro-4-nitrophenyl)azo]phenyl]imino]bisethanol
    2. Synonyms: 2,2'-[[4-[(2,6-dichloro-4-nitrophenyl)azo]phenyl]imino]bisethanol;Ethanol, 2,2-4-(2,6-dichloro-4-nitrophenyl)azophenyliminobis-
    3. CAS NO:63467-07-2
    4. Molecular Formula: C16H16Cl2N4O4
    5. Molecular Weight: 399.22864
    6. EINECS: 264-220-0
    7. Product Categories: Organics
    8. Mol File: 63467-07-2.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 624.8°Cat760mmHg
    3. Flash Point: 331.6°C
    4. Appearance: /
    5. Density: 1.46g/cm3
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 2,2'-[[4-[(2,6-dichloro-4-nitrophenyl)azo]phenyl]imino]bisethanol(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2,2'-[[4-[(2,6-dichloro-4-nitrophenyl)azo]phenyl]imino]bisethanol(63467-07-2)
    11. EPA Substance Registry System: 2,2'-[[4-[(2,6-dichloro-4-nitrophenyl)azo]phenyl]imino]bisethanol(63467-07-2)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 63467-07-2(Hazardous Substances Data)

63467-07-2 Usage

Uses

Used in Food Industry:
Tartrazine is used as a colorant to enhance the visual appeal of food products, providing a bright yellow hue that can make products more attractive to consumers. Its synthetic nature ensures a consistent color, which is crucial for maintaining a uniform appearance across batches.
Used in Pharmaceutical Industry:
In pharmaceuticals, Tartrazine serves as a coloring agent for medications, ensuring that pills and other formulations have a visually distinct and recognizable appearance. This can aid in product identification and consumer compliance with medication regimens.
Used in Cosmetic Products:
Tartrazine is utilized in the cosmetic industry to impart a yellow shade to various products, such as creams, lotions, and makeup. Its vibrant color contributes to the aesthetic appeal of these products, making them more desirable to consumers.
Used as a pH Indicator:
Due to its color-changing properties in response to pH variations, Tartrazine is employed as a pH indicator in scientific and industrial applications. This allows for the monitoring and control of pH levels in various processes, ensuring optimal conditions for reactions or preservation.
Used in Printing Inks and Textile Dyes:
Tartrazine's intense color makes it suitable for use in the production of printing inks and textile dyes. Its ability to provide a consistent and long-lasting color is valuable in these industries, where colorfastness and vibrancy are paramount.
Despite its widespread use, Tartrazine has been the subject of controversy due to potential health concerns. Studies have suggested possible links to behavioral issues in children, allergies, and hyperactivity. Consequently, some countries have imposed restrictions on its use in certain products. The safety of Tartrazine continues to be a topic of debate within the scientific community, and its use is carefully monitored and regulated in various industries.

Check Digit Verification of cas no

The CAS Registry Mumber 63467-07-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,4,6 and 7 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 63467-07:
(7*6)+(6*3)+(5*4)+(4*6)+(3*7)+(2*0)+(1*7)=132
132 % 10 = 2
So 63467-07-2 is a valid CAS Registry Number.

63467-07-2SDS

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 2-[4-[(2,6-dichloro-4-nitrophenyl)diazenyl]-N-(2-hydroxyethyl)anilino]ethanol

1.2 Other means of identification

Product number -
Other names EINECS 264-220-0

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:63467-07-2 SDS

63467-07-2Upstream product

63467-07-2Downstream Products

63467-07-2Relevant articles and documents

Clean preparation method for weakly alkaline arylamine azo disperse dye

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Paragraph 0047; 0048; 0049; 0050; 0051; 0057; 0058, (2017/01/02)

The present invention provides a clean preparation method for weakly alkaline arylamine azo disperse dye. The method is characterized in that when a weakly alkaline arylamine diazonium double salt solid is coupled with a coupling component, the coupling component is pretreated to obtain a fine particle dispersion to be coupled with the weakly alkaline arylamine diazonium double salt; and the generated disperse dye is precipitated from the coupling system and is filtered and dried, thereby obtaining the weakly alkaline arylamine azo disperse dye. According to the preparation method provided by the present invention, by using a stable double salt structure of a diazonium salt, during the coupling, the process of adding acid for dissolution can be omitted; the coupling is performed at the normal temperature, and extra cooling is not required; and the method has a broad application prospect.

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