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Solvent Red 197 is a brilliant red powder with a bluish shade, characterized by its water solubility of up to 1.0%, water resistance of 5, and a tinging strength of 100-105%. It exhibits heat resistance of at least 300°C, light fastness of 7, and moderate resistance to both acid and alkali with a rating of 5. The density of Solvent Red 197 is 1.25 g/cm3, and it has a maximum residue of 5.0% on an 80 mesh screen.

52372-39-1

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52372-39-1 Usage

Uses

Used in Dye Industry:
Solvent Red 197 is used as a colorant for its brilliant red hue and bluish shade, providing high tinging strength and resistance to various conditions such as heat, light, and water.
Used in Plastics and Rubber Industry:
Solvent Red 197 is used as an additive to impart color and enhance the appearance of plastics and rubber products, taking advantage of its heat and light resistance properties.
Used in Paint and Coatings Industry:
Solvent Red 197 is used as a pigment in the formulation of paints and coatings, offering a vibrant red color with good resistance to environmental factors.
Used in Textile Industry:
Solvent Red 197 is used as a dye for coloring fabrics, benefiting from its water resistance and ability to provide a consistent shade even under various conditions.

Flammability and Explosibility

Notclassified

TEST ITEMS

SPECIFICATION

HEAT RESISTANCE

300 °C min

LIGHT FASTNESS

7

ACID RESISTANCE

5

ALKALI RESISTANCE

5

DENSITY

1.25 g/cm 3

RESIDUE ON 80 MESH

5.0% max

VOLATITE 105 °C

1.0% max

Check Digit Verification of cas no

The CAS Registry Mumber 52372-39-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,2,3,7 and 2 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 52372-39:
(7*5)+(6*2)+(5*3)+(4*7)+(3*2)+(2*3)+(1*9)=111
111 % 10 = 1
So 52372-39-1 is a valid CAS Registry Number.
InChI:InChI=1/C23H19N5O/c1-3-27(4-2)15-10-9-14-11-16-21(29-20(14)12-15)17(13-24)22(25)28-19-8-6-5-7-18(19)26-23(16)28/h5-12,25H,3-4H2,1-2H3/b25-22+

52372-39-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name (7e)-3-(diethylamino)-7-imino-7h-chromeno[3',2':3,4]pyrido[1,2-a]benzimidazole-6-carbonitrile

1.2 Other means of identification

Product number -
Other names Solvent Red 197

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:52372-39-1 SDS

52372-39-1Relevant academic research and scientific papers

Construction of ratiometric hydrogen sulfide probe with two reaction sites and its applications in solution and in live cells

Fu, Deyang,Zhi,Lv,Luo, Yi,Xiong, Xiaoqing,Kang, Xiaohui,Hou, Wei,Yan, Jun,Zhao, Hongjuan,Zheng, Laijiu

, (2020)

Hydrogen sulfide (H2S), as the third multifunctional signaling biomolecule, it acts as a neuromodulator in the human brain and is recognized as an important gas transmitter in human physiology. The abnormal concentrations of H2S in human cells can result in several common diseases. Therefore, accurate, fast, and reliable methodologies are required for measuring the in vitro and in vivo concentrations of H2S to further investigate its function. In this study, a novel DR–SO2N3 fluorescent probe containing the fluorophore Disperse Red 277 and a sulfonyl azide group was developed and exploited based on the structural characteristic of Disperse Red 277 that contains the active site easily can be attacked by HS?. Therefore, this probe featured two reaction sites that involved the reduction and Michael addition of H2S and exhibited rapid ratiometric fluorescence changes and high selectivity towards H2S with a 619-fold enhancement factor. Further, the density functional theory (DFT)/time-dependent density functional theory (TDDFT) studies are conducted to understand the photophysical properties of DR–SO2N3 and the final product DRHS–SO2NH2, which makes the proposed mechanism more reasonable. Furthermore, the probe was successfully applied for the ratiometric fluorescence imaging of exogenous H2S in living cells.

Preparation and photophysical properties of thin films of coumarin dyes

Ibrayev, N. Kh.,Seliverstova,Alekseeva,Marinina,Savvina

, p. 1234 - 1238 (2013/07/19)

The results from investigating the photophysical properties of new coumarin dyes synthesized and incorporated into Langmuir-Blodgett films are presented. A method for forming monolayers on the surface of a water/air interface is proposed. The phase states of mixed monolayers on a water surface are studied. It is found that mixed monolayers of amphiphilic polyampholyte and dye allow us to obtain more stable and condensed films, relative to films of single components. The spectral and luminescent properties of synthesized dyes in solution and in Langmuir-Blodgett films are studied.

Articles Comprising Benzopyran Colorants, Method Of Manufacture, And Method Of Use

-

Page/Page column 7, (2008/06/13)

An article comprising the compound of Formula (I) wherein X is hydrogen or a radical of Formula (II), R1 independently at each occurrence is a C1-C20 aliphatic radical, a C3-C10 cycloaliphatic radical, or a C3-C10 aromatic radical; R2, R3, R4 and R5 are independently at each occurrence a halogen, a nitro group, a cyano group, a hydroxy group, a C1-C20 aliphatic radical, a C3-C20 cycloaliphatic radical, or a C6-C20 aromatic radical; and “n”, “q”, and “p” are each independently integers having a value of 0 to 3, and “m” is an integer having a value of 0 to 4.

BENZOPYRAN COLORANTS, METHOD OF MANUFACTURE, AND METHOD OF USE

-

, (2008/06/13)

A compound of Formula (I) wherein X is hydrogen or a radical of Formula (II), R1 independently at each occurrence is a C1-C20 aliphatic radical, a C3-C10 cycloaliphatic radical, or a C3-C10 aromatic radical; R2, R3, R4 and R5 are independently at each occurrence a halogen, a nitro group, a cyano group, a hydroxy group, a C1-C20 aliphatic radical, a C3-C20 cycloaliphatic radical, or a C6-C20 aromatic radical; and “n”, “q”, and “p” are each independently integers having a value of 0 to 3, and “m” is an integer having a value of 0 to 4.

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