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27908-75-4

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27908-75-4 Usage

Description

Solvent Yellow 157 is a brilliant green-yellow colored chemical compound with good light fastness and heat resistance properties. It has a melting point of 280°C and is insoluble in water but has well solubility in sodium carbonate (5%) and hydrochloric acid (5%).

Uses

Used in Dye Industry:
Solvent Yellow 157 is used as a coloring agent for various applications in the dye industry due to its brilliant green-yellow color and good light fastness properties.
Used in Plastic Industry:
Solvent Yellow 157 is used as an additive in the plastic industry to impart color and enhance the appearance of plastic products. Its heat resistance property makes it suitable for use in high-temperature processing.
Used in Textile Industry:
Solvent Yellow 157 is used as a dye in the textile industry for coloring fabrics. Its good light fastness ensures that the color remains vibrant even after exposure to sunlight.
Used in Paint Industry:
Solvent Yellow 157 is used as a pigment in the paint industry to provide a vibrant green-yellow color to the paint. Its heat resistance property makes it suitable for use in high-temperature applications.
Used in Ink Industry:
Solvent Yellow 157 is used as a colorant in the ink industry for producing inks with a brilliant green-yellow color. Its good light fastness ensures that the color remains stable over time.
Used in Cosmetic Industry:
Solvent Yellow 157 is used as a color additive in the cosmetic industry for products such as eyeshadows, lipsticks, and nail polishes. Its heat resistance and good light fastness properties make it suitable for use in cosmetic formulations.

Preparation

2-Methylquinoline and 4,5,6,7-Tetrachloroisobenzofuran-1,3-dione condensation.

Standard

Light Fastness

Melting point

Stable

ISO

Good

Check Digit Verification of cas no

The CAS Registry Mumber 27908-75-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,7,9,0 and 8 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 27908-75:
(7*2)+(6*7)+(5*9)+(4*0)+(3*8)+(2*7)+(1*5)=144
144 % 10 = 4
So 27908-75-4 is a valid CAS Registry Number.
InChI:InChI=1/C18H7Cl4NO2/c19-13-11-12(14(20)16(22)15(13)21)18(25)10(17(11)24)9-6-5-7-3-1-2-4-8(7)23-9/h1-6,10H

27908-75-4SDS

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 4,5,6,7-Tetrachloro-2-(2-quinolinyl)-1H-indene-1,3(2H)-dione

1.2 Other means of identification

Product number -
Other names 1H-Isoindol-1-one,4,5,6,7-tetrachloro-2,3-dihydro

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:27908-75-4 SDS

27908-75-4Downstream Products

27908-75-4Relevant articles and documents

PHENANTHROLINE COMPOUND AND COLORANT

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Paragraph 0068-0069; 0075-0076, (2017/08/02)

PROBLEM TO BE SOLVED: To provide a phenanthroline compound having a new skeleton available as a yellow pigment. SOLUTION: The phenanthroline compound is represented by the general formula in the figure. (In the general formula (1), R1 and R2 each independently represent a hydrogen atom, or an optionally substituted alkyl group, aryl group or indandione group, provided that at least one of R1 and R2 is the optionally substituted indandione group; and R3 and R4 each independently represent a hydrogen atom or a phenyl group.) SELECTED DRAWING: None COPYRIGHT: (C)2017,JPOandINPIT

Pigment dispersing agent, pigment composition and pigment dispersion

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Page/Page column 17-18, (2008/06/13)

A pigment dispersing agent wherein a quinophthalone structure is bonded to a triazine structure through an arylene group or a heteroaromatic ring and a basic functional group is bonded to triazine ring through a connecting group which pigment dispersing a

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