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82-38-2

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82-38-2 Usage

Description

Disperse Red 9 is a synthetic azo dye that is characterized by its bright red color with a blue hue. It is soluble in ethanol, acetone, and soluble fiber elements, slightly soluble in benzene and carbon tetrachloride, and insoluble in special solvents. It exhibits good levelness and a high improvement rate, making it suitable for various dyeing applications.

Uses

Used in Textile Industry:
Disperse Red 9 is used as a dyeing agent for polyester, polyamide fiber, acrylic, acetate fiber, and triacetate fiber. It provides good colorfastness properties, including ironing fastness, light fastness, perspiration fastness, and washing fastness, as per the ISO standards.
Used in Leather Industry:
Disperse Red 9 is used as a dyeing agent for sheepskin, providing a vibrant and long-lasting color.
Used in Plastic Industry:
Disperse Red 9 is used for coloring plastics, imparting a bright red hue and enhancing the appearance of plastic products.

Preparation

1-Chloroanthraquinone?or 9,10-Dioxo-9,10-dihydroanthracene-1-sulfonic acid?in pressure and in the presence of antioxidants with Methanamine for processing.

Synthesis Reference(s)

Organic Syntheses, Coll. Vol. 3, p. 573, 1955Synthetic Communications, 21, p. 1889, 1991 DOI: 10.1080/00397919108021779

Standard(Vinegar fiber)

Ironing Fastness

Fading

Stain

Purification Methods

Crystallise it to constant melting point from butan-1-ol, then from EtOH. It can be sublimed under vacuum. [Beilstein 7 IV 2574.]

Check Digit Verification of cas no

The CAS Registry Mumber 82-38-2 includes 5 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 2 digits, 8 and 2 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 82-38:
(4*8)+(3*2)+(2*3)+(1*8)=52
52 % 10 = 2
So 82-38-2 is a valid CAS Registry Number.
InChI:InChI=1/C15H11NO2/c1-16-12-8-4-7-11-13(12)15(18)10-6-3-2-5-9(10)14(11)17/h2-8,16H,1H3

82-38-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(Methylamino)anthraquinone

1.2 Other means of identification

Product number -
Other names 9,10-Anthracenedione, 1-(methylamino)-

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:82-38-2 SDS

82-38-2Relevant articles and documents

Ionic liquids as novel and recyclable reaction media for N-alkylation of amino-9,10-anthraquinones by trialkyl phosphites

Yavari, Issa,Kowsari, Elaheh

, p. 3753 - 3756 (2007)

Ionic liquids such as 1,3-dialkylimidazolium bromides make excellent catalysts and solvents for N-alkylation of amino-9,10-anthraquinones in the presence of trialkyl phosphites. For triethyl phosphite, [bpim][Br] gave better results. The ionic liquids are successfully regenerated and reused.

Method for synthesizing solvent dye intermediate

-

Paragraph 0026-0035, (2019/07/16)

The invention discloses a method for synthesizing a solvent dye intermediate. The dye intermediate is 1-methylaminoanthraquinone, and the method comprises the following steps: 1-aminoanthraquinone andchloromethane are used as the raw materials, and the target product is obtained by the condensation reaction under the action of a catalyst and an acid binding agent in a polar solvent. The route that 1-methylaminoanthraquinone is synthesized by using 1-aminoanthraquinone and chloromethane as the raw materials does not have nitrosamine formation, the high quality solvent dye intermediate is produced, and the quality of downstream products is improved. Moreover, the method uses ammonium chloride, ammonium acetate or ammonium nitrate as the reaction catalyst, the selectivity of the main productsecondary amine is improved, and the side reaction tertiary amine production is reduced.

Process for preparing substituted aminoanthraquinones

-

, (2008/06/13)

Substituted aminoanthraquinone compounds, which are used for dye stuffs or intermediate thereof, represented by the formula (II) STR1 wherein R3 represents a C1 -C6 alkyl group which may be substituted, X represents a hydrogen atom, --COR1 or --SO2 R2 wherein R1 and R2 each represents a substituted or unsubstituted C1 -C4 alkyl or C6 -C12 aryl group, and Y and Z represent independently a hydrogen atom, a halogen atom, a nitro group or a C1 -C4 alkyl group, is prepared by allowing anthraquinone compounds represented by the formula STR2 wherein X, Y and Z are as defined above, to react with alkylating agents in organic solvents in the presence of organic quaternary ammonium salts and alkalies.

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