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3468-63-1

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3468-63-1 Usage

Description

Pigment Orange 5 is an azo pigment, characterized by its orange powder appearance and yellowish shade. It is produced industrially through a diazotization and coupling sequence involving diazotized dinitroaniline and β-naphthol. This pigment exhibits a tinting strength of 100-105%, indicating its high color intensity.
Used in Paint and Coating Industry:
Pigment Orange 5 is used as a colorant for providing vibrant orange hues in various paint and coating applications. Its heat resistance of at least 140°C ensures stability under high temperatures, while its light fastness rating of 7 suggests good resistance to fading from sunlight exposure.
Used in Plastics Industry:
In the plastics industry, Pigment Orange 5 serves as a pigment for imparting orange coloration to plastic products. Its properties, such as acid and alkali resistance rated 5, make it suitable for use in environments with varying pH levels.
Used in Printing Ink Industry:
Pigment Orange 5 is utilized as a pigment in the formulation of printing inks. Its oil absorption of 35-40% and specific surface of 30 m2/g contribute to the ink's performance characteristics, such as flow and stability.
Used in Textile Industry:
In textile applications, Pigment Orange 5 is used for dyeing and printing processes to achieve orange-colored fabrics. The pigment's properties, including fastness to bleeding rated 5, ensure color consistency and resistance to bleeding when wet.
Overall, Pigment Orange 5 is a versatile azo pigment with a range of applications across various industries, including paint and coatings, plastics, printing inks, and textiles, due to its color intensity, stability, and resistance to environmental factors.

TEST ITEMS

SPECIFICATION

HEAT RESISTANCE

140 °C min

LIGHT FASTNESS

7

ACID RESISTANCE

5

ALKALI RESISTANCE

5

FASTNESS TO BLEEDING

5

OIL ABSORPTION

35-40%

SPECIFIC SURFACE

30 m 2 /g

DENSITY

1.50 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 3468-63-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,4,6 and 8 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 3468-63:
(6*3)+(5*4)+(4*6)+(3*8)+(2*6)+(1*3)=101
101 % 10 = 1
So 3468-63-1 is a valid CAS Registry Number.
InChI:InChI=1/C16H10N4O5/c21-15-8-5-10-3-1-2-4-12(10)16(15)18-17-13-7-6-11(19(22)23)9-14(13)20(24)25/h1-9,17H

3468-63-1 Well-known Company Product Price

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  • Sigma-Aldrich

  • (09215)  Pigment Orange 5  analytical standard

  • 3468-63-1

  • 09215-25MG

  • 1,437.93CNY

  • Detail

3468-63-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name Pigment Orange 5

1.2 Other means of identification

Product number -
Other names Permanent Orange

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only. Pigments
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:3468-63-1 SDS

3468-63-1Synthetic route

β-naphthol
135-19-3

β-naphthol

2,4-Dinitroanilin
97-02-9

2,4-Dinitroanilin

C.I. pigment orange 5
3468-63-1

C.I. pigment orange 5

Conditions
ConditionsYield
Stage #1: 2,4-Dinitroanilin With sulfuric acid; sodium nitrite In water at 20℃; for 0.333333h;
Stage #2: β-naphthol In water at 20℃; for 1h; Time;
99%
Stage #1: 2,4-Dinitroanilin With sulfuric acid; sodium nitrite In water at 0℃; for 0.333333h; Green chemistry;
Stage #2: β-naphthol In water at 20℃; for 1h; Green chemistry;
99%
With nitrosylsulfuric acid; ethanol
With nitrosylpolyphosphoric acid 1.) glacial acetic acid, 40-70 deg C, 0.5 h; Yield given. Multistep reaction;
2,4-Dinitroanilin
97-02-9

2,4-Dinitroanilin

C.I. pigment orange 5
3468-63-1

C.I. pigment orange 5

Conditions
ConditionsYield
With chloroform; BF3-N2O3 und Behandeln des Reaktionsprodukts mit <2>Naphthol in wss.NaOH;
(2-naphthoyl)oxyacetic acid
120-23-0

(2-naphthoyl)oxyacetic acid

2,4-dinitro-benzenediazonium-sulfate

2,4-dinitro-benzenediazonium-sulfate

C.I. pigment orange 5
3468-63-1

C.I. pigment orange 5

Conditions
ConditionsYield
With acetic acid
2-Methoxynaphthalene
93-04-9

2-Methoxynaphthalene

2,4-dinitro-benzenediazonium-sulfate

2,4-dinitro-benzenediazonium-sulfate

C.I. pigment orange 5
3468-63-1

C.I. pigment orange 5

Conditions
ConditionsYield
With acetic acid
2-ethoxynaphthalene
93-18-5

2-ethoxynaphthalene

2,4-dinitro-benzenediazonium-sulfate

2,4-dinitro-benzenediazonium-sulfate

C.I. pigment orange 5
3468-63-1

C.I. pigment orange 5

Conditions
ConditionsYield
With acetic acid
1-bromo-2-methoxynaphthalene
3401-47-6

1-bromo-2-methoxynaphthalene

2,4-dinitro-benzenediazonium-sulfate

2,4-dinitro-benzenediazonium-sulfate

C.I. pigment orange 5
3468-63-1

C.I. pigment orange 5

Conditions
ConditionsYield
With acetic acid
2-(4-methoxyphenoxy)naphthalene
40843-59-2

2-(4-methoxyphenoxy)naphthalene

2,4-dinitro-benzenediazonium-sulfate

2,4-dinitro-benzenediazonium-sulfate

C.I. pigment orange 5
3468-63-1

C.I. pigment orange 5

Conditions
ConditionsYield
With acetic acid
2-butoxynaphthalene
10484-56-7

2-butoxynaphthalene

2,4-dinitro-benzenediazonium-sulfate

2,4-dinitro-benzenediazonium-sulfate

C.I. pigment orange 5
3468-63-1

C.I. pigment orange 5

Conditions
ConditionsYield
With acetic acid
β-naphthol
135-19-3

β-naphthol

2.4-dinitro-benzenediazonium sulfate

2.4-dinitro-benzenediazonium sulfate

C.I. pigment orange 5
3468-63-1

C.I. pigment orange 5

Conditions
ConditionsYield
With alkali

3468-63-1Downstream Products

3468-63-1Relevant articles and documents

A quantitative one-pot synthesis method for industrial azo pigments with recyclable wastewater

Feng, Guangyuan,Zhu, Meiling,Liu, Lei,Li, Chunbao

supporting information, p. 1769 - 1776 (2019/04/08)

Most industrial azo pigments are synthesized by diazotization in one pot and then coupling in another. This two-pot process has been transformed into a one-pot method by adding granular PTFE (polytetrafluoroethylene) to a mechanically agitated aqueous mixture of NaNO2, HCl, a diazo component and a coupling component. This method avoids the step of using a base or a surfactant to dissolve the coupling component. The reactions were fast and quantitative. The granular PTFE, wastewater and excess HCl were then reused 11 times without deteriorating the reaction rate and product purity. Altogether, 22 industrial pigments and 3 azo compounds were synthesized and the reaction can produce up to 22.7 g of product in the laboratory. Some reactions require less than 2 equiv. of HCl and a mechanism explaining this is proposed. In addition, an o-nitro group effect is advanced to explain the differences in coupling reaction rates for o-, m- and p-nitroaniline.

Method used for synthesizing azo compound using solid particle one kettle method

-

Paragraph 0222; 0223; 0224; 0229; 0232; 0235, (2019/01/07)

The invention relates to a method used for synthesizing an azo compound using solid particle one kettle method. The method comprises following steps: solid particles are introduced into a reaction container, an inorganic acid, an aromatic primary amine, sodium nitrite, water, and a coupling component are added, mechanism stirring is carried out, when the reaction is monitored to be finished, filtering and rinsing are carried out, and the obtained filter cake is a finished product; or the solid particles are introduced into the reaction container, the inorganic acid, the aromatic primary amine,sodium nitrite, and water are added, mechanical stirring is carried out, after complete conversion of the aromatic primary amine, the coupling component is added, mechanical stirring is carried out,when the reaction is monitored to be finished, filtering and rinsing are carried out, and the obtained filter cake is a finished product. The solid particles are preferably selected from polytetrafluoroethylene particles, haw seeds, or stainless steel sand. The solid particles are added into the reaction system to promote reaction, no pre-heating or alkali adding dissolving of diazo components orthe coupling component is needed; most reaction is finished in 1h; reaction time is short; product quality is high; and reaction filtrate and excess inorganic acid can be recycled for a plurality of times.

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