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Pigment Red 122 is a red organic pigment characterized by its vibrant, high-strength red color, excellent lightfastness, and weather resistance. It is composed of a metal salt complex of 1,4-diketopyrrolo[3,4-c]pyrrole and benzimidazolone, which contributes to its intense color and suitability for a wide range of industrial and consumer products. With its low toxicity, it is considered safe for various applications.

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  • 980-26-7 Structure
  • Basic information

    1. Product Name: Pigment Red 122
    2. Synonyms: TRANSQUINACRIDONE;acramin scarlet ldcn;Pigment red 122 (C.I. 73915);[2,3-b]Acridine-7,14-dione, 5,12-dihydro-2,9-dimethyl-quino;5,12-Dihydro-2,9-dimethylquino[2,3-b]acridine-7,14-dione;C.I. 73915;Pigment Red 122;Quindo Red -W
    3. CAS NO:980-26-7
    4. Molecular Formula: C22H16N2O2
    5. Molecular Weight: 340.37
    6. EINECS: 213-561-3
    7. Product Categories: N/A
    8. Mol File: 980-26-7.mol
  • Chemical Properties

    1. Melting Point: 440℃
    2. Boiling Point: 601.6 °C at 760 mmHg
    3. Flash Point: 221.4 °C
    4. Appearance: chip
    5. Density: 1.307 g/cm3
    6. Vapor Pressure: 1.98E-14mmHg at 25°C
    7. Refractive Index: 1.676
    8. Storage Temp.: Keep in dark place,Inert atmosphere,Room temperature
    9. Solubility: N/A
    10. PKA: -2.49±0.20(Predicted)
    11. CAS DataBase Reference: Pigment Red 122(CAS DataBase Reference)
    12. NIST Chemistry Reference: Pigment Red 122(980-26-7)
    13. EPA Substance Registry System: Pigment Red 122(980-26-7)
  • 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: 980-26-7(Hazardous Substances Data)

980-26-7 Usage

Uses

Used in Paint Industry:
Pigment Red 122 is used as a colorant for its vibrant red hue and excellent lightfastness, providing durable and long-lasting color in various paint formulations.
Used in Ink Industry:
As a pigment in inks, Pigment Red 122 offers a strong red color with resistance to fading, making it ideal for printing applications that require color stability and durability.
Used in Plastics Industry:
Pigment Red 122 is utilized as a coloring agent in the plastics industry, imparting a consistent and long-lasting red shade to plastic products while maintaining its resistance to light and weather exposure.
Used in Textile Industry:
In textiles, Pigment Red 122 serves as a high-strength red dye, offering excellent colorfastness and resistance to washing and environmental factors, ensuring the color remains vibrant over time.
Overall, Pigment Red 122's unique properties make it a versatile and valuable pigment for various industries, providing a striking red color with enduring performance.

Check Digit Verification of cas no

The CAS Registry Mumber 980-26-7 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 9,8 and 0 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 980-26:
(5*9)+(4*8)+(3*0)+(2*2)+(1*6)=87
87 % 10 = 7
So 980-26-7 is a valid CAS Registry Number.
InChI:InChI=1/C22H16N2O2/c1-11-3-5-17-13(7-11)21(25)15-9-20-16(10-19(15)23-17)22(26)14-8-12(2)4-6-18(14)24-20/h3-10H,1-2H3,(H,23,25)(H,24,26)

980-26-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name Pigment Red 122

1.2 Other means of identification

Product number -
Other names 8 PIGMENT RED 8

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:980-26-7 SDS

980-26-7Synthetic route

2,5-di(4'-methylphenylamino)terephthalic acid
10291-28-8

2,5-di(4'-methylphenylamino)terephthalic acid

C.I. Pigment Red 122
980-26-7

C.I. Pigment Red 122

Conditions
ConditionsYield
With polyphosphoric acid PPA at 125℃; for 6h; Dieckmann Condensation;99.59%
With phosphoric acid; phosphorus pentoxide at 20 - 130℃; for 2.25h; Product distribution / selectivity;97%
With PPA at 20 - 130℃; for 2.25h; Product distribution / selectivity;85%
2,9-dimethyl-6,13-dihydroquinacridone
13796-22-0

2,9-dimethyl-6,13-dihydroquinacridone

C.I. Pigment Red 122
980-26-7

C.I. Pigment Red 122

Conditions
ConditionsYield
With dihydrogen peroxide; potassium hydroxide at 90 - 110℃; for 4h; pH=10 - 11; pH-value; Temperature;91.13%
With sodium hydroxide; dihydrogen peroxide In water; polyethylene glycol 400 at 20 - 60℃; for 1h; Product distribution / selectivity;
C21H18N2O4
67906-32-5

C21H18N2O4

2,5-di(phenylamino)-terephthalic acid
10109-95-2

2,5-di(phenylamino)-terephthalic acid

2,5-di(4'-methylphenylamino)terephthalic acid
10291-28-8

2,5-di(4'-methylphenylamino)terephthalic acid

A

Quinacridone
1047-16-1

Quinacridone

B

C.I. Pigment Red 122
980-26-7

C.I. Pigment Red 122

C

5,12-dihydro-2-methylquino[2,3-b]acridine-7,14-dione
10228-01-0

5,12-dihydro-2-methylquino[2,3-b]acridine-7,14-dione

Conditions
ConditionsYield
With PPA at 90 - 125℃; for 3h;
With PPA at 90 - 125℃; for 3h;
With PPA at 90 - 125℃; for 3h;
With PPA at 90 - 125℃; for 3h;
dimethyl 2,5-dioxocyclohexane-1,4-dicarboxylate
6289-46-9

dimethyl 2,5-dioxocyclohexane-1,4-dicarboxylate

p-toluidine
106-49-0

p-toluidine

C.I. Pigment Red 122
980-26-7

C.I. Pigment Red 122

Conditions
ConditionsYield
Stage #1: dimethyl 2,5-dioxocyclohexane-1,4-dicarboxylate; p-toluidine With phosphoric acid at 20 - 100℃; for 4h;
Stage #2: With sodium hydroxide; sodium 3-nitrobenzenesulfonate In water for 4h; Heating / reflux;
Stage #3: With sulfuric acid pH=3; Product distribution / selectivity;
2,5-di-p-toluidino-terephthalic acid dimethyl ester
114508-42-8

2,5-di-p-toluidino-terephthalic acid dimethyl ester

C.I. Pigment Red 122
980-26-7

C.I. Pigment Red 122

Conditions
ConditionsYield
With toluene-4-sulfonic acid for 0.166667h; Product distribution / selectivity; Heating / reflux;
Multi-step reaction with 2 steps
1: sodium hydroxide / 3 h / 110 °C / Reflux
2: polyphosphoric acid PPA / 6 h / 125 °C
View Scheme
2,5-di(4'-methylphenylamino)terephthalic acid
10291-28-8

2,5-di(4'-methylphenylamino)terephthalic acid

C22H17N3O3

C22H17N3O3

A

C.I. Pigment Red 122
980-26-7

C.I. Pigment Red 122

B

C21H13N3O2

C21H13N3O2

Conditions
ConditionsYield
With polyphosphoric acid at 120 - 130℃; for 2h;
C.I. Pigment Red 122
980-26-7

C.I. Pigment Red 122

4-Chlorobutanoyl chloride
4635-59-0

4-Chlorobutanoyl chloride

2,9-dimethyl-3,10-di(4-chlorobutyryl)quinacridone

2,9-dimethyl-3,10-di(4-chlorobutyryl)quinacridone

Conditions
ConditionsYield
With zirconium chloride In tetrachloromethane at 10 - 60℃; for 48h;90%
1 ,6-dibromohexane
629-03-8

1 ,6-dibromohexane

C.I. Pigment Red 122
980-26-7

C.I. Pigment Red 122

2,9-dimethyl-5,12-bis(6-bromohexyl)-5,12-dihydroquino[2,3-b]acridine-7,14-dione

2,9-dimethyl-5,12-bis(6-bromohexyl)-5,12-dihydroquino[2,3-b]acridine-7,14-dione

Conditions
ConditionsYield
With sodium hydride In tetrahydrofuran for 24h; Reflux;65%
Acetyl bromide
506-96-7

Acetyl bromide

C.I. Pigment Red 122
980-26-7

C.I. Pigment Red 122

C24H18N2O3
1415414-23-1

C24H18N2O3

Conditions
ConditionsYield
With sodium hydride In 1-methyl-pyrrolidin-2-one38%
propanoyl bromide
598-22-1

propanoyl bromide

C.I. Pigment Red 122
980-26-7

C.I. Pigment Red 122

C25H20N2O3
1415414-24-2

C25H20N2O3

Conditions
ConditionsYield
With sodium hydride In 1-methyl-pyrrolidin-2-one36%
C.I. Pigment Red 122
980-26-7

C.I. Pigment Red 122

bromoacetic acid methyl ester
96-32-2

bromoacetic acid methyl ester

C25H20N2O4
1415414-25-3

C25H20N2O4

Conditions
ConditionsYield
With sodium hydride In 1-methyl-pyrrolidin-2-one28%
C.I. Pigment Red 122
980-26-7

C.I. Pigment Red 122

ethyl bromoacetate
105-36-2

ethyl bromoacetate

C26H22N2O4
1415414-26-4

C26H22N2O4

Conditions
ConditionsYield
With sodium hydride In 1-methyl-pyrrolidin-2-one25%
1-bromo dodecane
112-29-8

1-bromo dodecane

C.I. Pigment Red 122
980-26-7

C.I. Pigment Red 122

C32H36N2O2
1415414-22-0

C32H36N2O2

Conditions
ConditionsYield
With sodium hydride In 1-methyl-pyrrolidin-2-one23%
1-bromo-octane
111-83-1

1-bromo-octane

C.I. Pigment Red 122
980-26-7

C.I. Pigment Red 122

2,9-dimethyl-5-octylquinolino[2,3-b]acridine-7,14(5H,12H)-dione
1415414-21-9

2,9-dimethyl-5-octylquinolino[2,3-b]acridine-7,14(5H,12H)-dione

Conditions
ConditionsYield
Stage #1: C.I. Pigment Red 122 With sodium hydride In 1-methyl-pyrrolidin-2-one at 20℃; for 2h;
Stage #2: 1-bromo-octane In 1-methyl-pyrrolidin-2-one at 70℃; for 20h;
21%
C.I. Pigment Red 122
980-26-7

C.I. Pigment Red 122

appr. radical-cations and -anions

appr. radical-cations and -anions

Conditions
ConditionsYield
In dichloromethane electrochemical reduction i.e. oxidation, tetrabutylammonium perchlorate as electrolyte, platinum electrode, products investigated by ESR-methods;
In various solvent(s) at 25℃; Irradiation; reaction products investigated by ESR-methods;
2,5-di(4'-methylphenylamino)terephthalic acid
10291-28-8

2,5-di(4'-methylphenylamino)terephthalic acid

C.I. Pigment Red 122
980-26-7

C.I. Pigment Red 122

Conditions
ConditionsYield
With polyphosphoric acid PPA at 125℃; for 6h; Dieckmann Condensation;99.59%
With phosphoric acid; phosphorus pentoxide at 20 - 130℃; for 2.25h; Product distribution / selectivity;97%
With PPA at 20 - 130℃; for 2.25h; Product distribution / selectivity;85%
2,9-dimethyl-6,13-dihydroquinacridone
13796-22-0

2,9-dimethyl-6,13-dihydroquinacridone

C.I. Pigment Red 122
980-26-7

C.I. Pigment Red 122

Conditions
ConditionsYield
With dihydrogen peroxide; potassium hydroxide at 90 - 110℃; for 4h; pH=10 - 11; pH-value; Temperature;91.13%
With sodium hydroxide; dihydrogen peroxide In water; polyethylene glycol 400 at 20 - 60℃; for 1h; Product distribution / selectivity;
C21H18N2O4
67906-32-5

C21H18N2O4

2,5-di(phenylamino)-terephthalic acid
10109-95-2

2,5-di(phenylamino)-terephthalic acid

2,5-di(4'-methylphenylamino)terephthalic acid
10291-28-8

2,5-di(4'-methylphenylamino)terephthalic acid

A

Quinacridone
1047-16-1

Quinacridone

B

C.I. Pigment Red 122
980-26-7

C.I. Pigment Red 122

C

5,12-dihydro-2-methylquino[2,3-b]acridine-7,14-dione
10228-01-0

5,12-dihydro-2-methylquino[2,3-b]acridine-7,14-dione

Conditions
ConditionsYield
With PPA at 90 - 125℃; for 3h;
With PPA at 90 - 125℃; for 3h;
With PPA at 90 - 125℃; for 3h;
With PPA at 90 - 125℃; for 3h;
dimethyl 2,5-dioxocyclohexane-1,4-dicarboxylate
6289-46-9

dimethyl 2,5-dioxocyclohexane-1,4-dicarboxylate

p-toluidine
106-49-0

p-toluidine

C.I. Pigment Red 122
980-26-7

C.I. Pigment Red 122

Conditions
ConditionsYield
Stage #1: dimethyl 2,5-dioxocyclohexane-1,4-dicarboxylate; p-toluidine With phosphoric acid at 20 - 100℃; for 4h;
Stage #2: With sodium hydroxide; sodium 3-nitrobenzenesulfonate In water for 4h; Heating / reflux;
Stage #3: With sulfuric acid pH=3; Product distribution / selectivity;
2,5-di-p-toluidino-terephthalic acid dimethyl ester
114508-42-8

2,5-di-p-toluidino-terephthalic acid dimethyl ester

C.I. Pigment Red 122
980-26-7

C.I. Pigment Red 122

Conditions
ConditionsYield
With toluene-4-sulfonic acid for 0.166667h; Product distribution / selectivity; Heating / reflux;
Multi-step reaction with 2 steps
1: sodium hydroxide / 3 h / 110 °C / Reflux
2: polyphosphoric acid PPA / 6 h / 125 °C
View Scheme
2,5-di(4'-methylphenylamino)terephthalic acid
10291-28-8

2,5-di(4'-methylphenylamino)terephthalic acid

C22H17N3O3

C22H17N3O3

A

C.I. Pigment Red 122
980-26-7

C.I. Pigment Red 122

B

C21H13N3O2

C21H13N3O2

Conditions
ConditionsYield
With polyphosphoric acid at 120 - 130℃; for 2h;
C.I. Pigment Red 122
980-26-7

C.I. Pigment Red 122

4-Chlorobutanoyl chloride
4635-59-0

4-Chlorobutanoyl chloride

2,9-dimethyl-3,10-di(4-chlorobutyryl)quinacridone

2,9-dimethyl-3,10-di(4-chlorobutyryl)quinacridone

Conditions
ConditionsYield
With zirconium chloride In tetrachloromethane at 10 - 60℃; for 48h;90%
1 ,6-dibromohexane
629-03-8

1 ,6-dibromohexane

C.I. Pigment Red 122
980-26-7

C.I. Pigment Red 122

2,9-dimethyl-5,12-bis(6-bromohexyl)-5,12-dihydroquino[2,3-b]acridine-7,14-dione

2,9-dimethyl-5,12-bis(6-bromohexyl)-5,12-dihydroquino[2,3-b]acridine-7,14-dione

Conditions
ConditionsYield
With sodium hydride In tetrahydrofuran for 24h; Reflux;65%
Acetyl bromide
506-96-7

Acetyl bromide

C.I. Pigment Red 122
980-26-7

C.I. Pigment Red 122

C24H18N2O3
1415414-23-1

C24H18N2O3

Conditions
ConditionsYield
With sodium hydride In 1-methyl-pyrrolidin-2-one38%
propanoyl bromide
598-22-1

propanoyl bromide

C.I. Pigment Red 122
980-26-7

C.I. Pigment Red 122

C25H20N2O3
1415414-24-2

C25H20N2O3

Conditions
ConditionsYield
With sodium hydride In 1-methyl-pyrrolidin-2-one36%
C.I. Pigment Red 122
980-26-7

C.I. Pigment Red 122

bromoacetic acid methyl ester
96-32-2

bromoacetic acid methyl ester

C25H20N2O4
1415414-25-3

C25H20N2O4

Conditions
ConditionsYield
With sodium hydride In 1-methyl-pyrrolidin-2-one28%
C.I. Pigment Red 122
980-26-7

C.I. Pigment Red 122

ethyl bromoacetate
105-36-2

ethyl bromoacetate

C26H22N2O4
1415414-26-4

C26H22N2O4

Conditions
ConditionsYield
With sodium hydride In 1-methyl-pyrrolidin-2-one25%
1-bromo dodecane
112-29-8

1-bromo dodecane

C.I. Pigment Red 122
980-26-7

C.I. Pigment Red 122

C32H36N2O2
1415414-22-0

C32H36N2O2

Conditions
ConditionsYield
With sodium hydride In 1-methyl-pyrrolidin-2-one23%
1-bromo-octane
111-83-1

1-bromo-octane

C.I. Pigment Red 122
980-26-7

C.I. Pigment Red 122

2,9-dimethyl-5-octylquinolino[2,3-b]acridine-7,14(5H,12H)-dione
1415414-21-9

2,9-dimethyl-5-octylquinolino[2,3-b]acridine-7,14(5H,12H)-dione

Conditions
ConditionsYield
Stage #1: C.I. Pigment Red 122 With sodium hydride In 1-methyl-pyrrolidin-2-one at 20℃; for 2h;
Stage #2: 1-bromo-octane In 1-methyl-pyrrolidin-2-one at 70℃; for 20h;
21%
C.I. Pigment Red 122
980-26-7

C.I. Pigment Red 122

appr. radical-cations and -anions

appr. radical-cations and -anions

Conditions
ConditionsYield
In dichloromethane electrochemical reduction i.e. oxidation, tetrabutylammonium perchlorate as electrolyte, platinum electrode, products investigated by ESR-methods;
In various solvent(s) at 25℃; Irradiation; reaction products investigated by ESR-methods;
C.I. Pigment Red 122
980-26-7

C.I. Pigment Red 122

C22H14N2O2(2-)*2Na(1+)

C22H14N2O2(2-)*2Na(1+)

Conditions
ConditionsYield
With sodium t-butanolate In tert-butyl alcohol at 30 - 90℃; under 37.5038 - 600.06 Torr;
formaldehyd
50-00-0

formaldehyd

C.I. Pigment Red 122
980-26-7

C.I. Pigment Red 122

sodium 1-naphthalenesulfonate
130-14-3

sodium 1-naphthalenesulfonate

2-naphthalenesulfonic acid sodium salt
532-02-5

2-naphthalenesulfonic acid sodium salt

poly(formaldehyde-co-1-naphtalene sulfonic acid sodium salt-co-2-naphtalene sulfonic acid sodium salt); 2,9-dimethylquinacridone; mixture of

poly(formaldehyde-co-1-naphtalene sulfonic acid sodium salt-co-2-naphtalene sulfonic acid sodium salt); 2,9-dimethylquinacridone; mixture of

Conditions
ConditionsYield
Stage #1: C.I. Pigment Red 122 With sulfuric acid at 40 - 45℃; for 0.166667h;
Stage #2: sodium 1-naphthalenesulfonate; 2-naphthalenesulfonic acid sodium salt In water at 40 - 45℃; for 0.5h;
Stage #3: formaldehyd In water at 58 - 60℃; for 1h;
polyoxyethylene lauryl ether

polyoxyethylene lauryl ether

[1,3]-dioxolan-2-one
96-49-1

[1,3]-dioxolan-2-one

methanesulfonic acid
75-75-2

methanesulfonic acid

polyoxycetyl ether

polyoxycetyl ether

C.I. Pigment Red 122
980-26-7

C.I. Pigment Red 122

Reaxys ID: 20190102

Reaxys ID: 20190102

Conditions
ConditionsYield
Stage #1: methanesulfonic acid; C.I. Pigment Red 122 at 120℃; for 0.333333h;
Stage #2: polyoxyethylene lauryl ether; [1,3]-dioxolan-2-one; polyoxycetyl ether In water; acetonitrile at 20℃;
trimethylene carbonate
2453-03-4

trimethylene carbonate

methanesulfonic acid
75-75-2

methanesulfonic acid

polyoxycetyl ether

polyoxycetyl ether

C.I. Pigment Red 122
980-26-7

C.I. Pigment Red 122

acetic acid
64-19-7

acetic acid

Reaxys ID: 20190098

Reaxys ID: 20190098

Conditions
ConditionsYield
Stage #1: methanesulfonic acid; C.I. Pigment Red 122 at 150℃; for 0.333333h;
Stage #2: trimethylene carbonate; polyoxycetyl ether; acetic acid In methanol; water at 20℃;
C.I. Pigment Red 122
980-26-7

C.I. Pigment Red 122

C46H66N6O4(2+)*2Cl(1-)

C46H66N6O4(2+)*2Cl(1-)

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: zirconium chloride / tetrachloromethane / 48 h / 10 - 60 °C
2: acetonitrile / 8 h / Reflux
View Scheme
C.I. Pigment Red 122
980-26-7

C.I. Pigment Red 122

C48H72N6O4(4+)*2O4S(2-)

C48H72N6O4(4+)*2O4S(2-)

Conditions
ConditionsYield
Multi-step reaction with 3 steps
1: zirconium chloride / tetrachloromethane / 48 h / 10 - 60 °C
2: acetonitrile / 8 h / Reflux
3: acetonitrile / 4 h / Reflux
View Scheme
C.I. Pigment Red 122
980-26-7

C.I. Pigment Red 122

C55H104N2O23

C55H104N2O23

A

C132H218N4O48

C132H218N4O48

B

C77H117N3O25

C77H117N3O25

Conditions
ConditionsYield
Stage #1: C55H104N2O23 With hydrogenchloride; sodium nitrite In water for 0.333333h;
Stage #2: C.I. Pigment Red 122 In water at 50℃; pH=5 - 6;
C.I. Pigment Red 122
980-26-7

C.I. Pigment Red 122

C102H198N2O43

C102H198N2O43

C124H211N3O45

C124H211N3O45

Conditions
ConditionsYield
Stage #1: C102H198N2O43 With hydrogenchloride; sodium nitrite In water for 0.333333h;
Stage #2: C.I. Pigment Red 122 In water at 50℃; pH=5 - 6;
C.I. Pigment Red 122
980-26-7

C.I. Pigment Red 122

C148H290N2O67

C148H290N2O67

C170H303N3O69

C170H303N3O69

Conditions
ConditionsYield
Stage #1: C148H290N2O67 With hydrogenchloride; sodium nitrite In water for 0.333333h;
Stage #2: C.I. Pigment Red 122 In water at 50℃; pH=5 - 6;
1-bromo-octane
111-83-1

1-bromo-octane

C.I. Pigment Red 122
980-26-7

C.I. Pigment Red 122

2,9-dimethyl-5,12-dioctylquinolino[2,3-b]acridine-7,14(5H,12H)-dione

2,9-dimethyl-5,12-dioctylquinolino[2,3-b]acridine-7,14(5H,12H)-dione

Conditions
ConditionsYield
With N,N,N,N,N,N-hexamethylphosphoric triamide; tetrabutylammomium bromide; sodium hydride In mineral oil; benzene at 20 - 50℃; for 105h;0.44 g
C.I. Pigment Red 122
980-26-7

C.I. Pigment Red 122

2-(2,9-dimethyl-5,12-dioctyl-14-oxoquinolino[2,3-b]acridin-7(5H,12H,14H)-ylidene)malononitrile

2-(2,9-dimethyl-5,12-dioctyl-14-oxoquinolino[2,3-b]acridin-7(5H,12H,14H)-ylidene)malononitrile

Conditions
ConditionsYield
Multi-step reaction with 3 steps
1: N,N,N,N,N,N-hexamethylphosphoric triamide; sodium hydride; tetrabutylammomium bromide / benzene; mineral oil / 105 h / 20 - 50 °C
2: trichlorophosphate; N,N-dimethyl-formamide / 1,2-dichloro-ethane / 2 h / 60 °C
3: 2,4,6-trimethyl-pyridine / 2 h / 20 °C
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980-26-7Downstream Products

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Production method of quinacridone pigment or mixed crystal pigment thereof

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Paragraph 0017-0018; 0019-0020; 0025-0026; 0027-0034, (2020/09/16)

The invention belongs to the field of pigments, and relates to a production method of a quinacridone pigment or a mixed crystal pigment thereof, namely an environment-friendly and economical production method of the quinacridone pigment. The method comprises the following steps: cyclizing diphenylamino terephthalic acid or a derivative thereof in a formula (2); hydrolyzing the reaction mixture obtained by cyclization with water at 0-100 DEG C; separating out a crude pigment obtained in this way, then pulping the crude pigment in an aqueous medium without any additive, completing crystal form transformation of the pigment and curing of pigment particles at 120-170 DEG C in a closed reaction kettle, then directly separating or adding a surface modifier for surface modification, and then separating to obtain the pigment. Crystal form transformation and pigment particle curing are completely completed in an aqueous medium, and the method is environmentally friendly and low in cost.

Preparation method of 2,9-dimethyl quinacridone purplish red pigment

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Paragraph 0023-0038, (2020/05/01)

The invention discloses a preparation method of a 2,9-dimethyl quinacridone purplish red pigment. The 2,9-dimethyl quinacridone purplish red pigment is prepared by adopting a ring-closure reaction atfirst and an oxidation process next. The method comprises the following steps: adding 2,9-dimethyl-6,13-dihydroquinacridone obtained after a condensation reaction and the ring-closure reaction into areaction container; then adding a catalyst into the reaction container, adjusting a pH value to 7-11 by using a dilute alkali solution, and carrying out heating to 90 DEG C; slowly adding a hydrogen peroxide solution into the reaction container, controlling the adding molar ratio of hydrogen peroxide to the catalyst to 2, 9-dimethyl-6,13-dihydroquinacridone, continuing to heat to 105-140 DEG C, keeping the temperature, conducting a reaction for 3-4.5 hours and terminating the reaction; cooling a reaction solution to 80 DEG C, pouring the reaction solution into a beaker, adding cold water withthe same volume as the reaction solution, carrying out stirring, conducting cooling to room temperature, performing filtering, washing a filter cake with methanol, carrying out pulping for 1 hour, then conducing filtering, and carrying out top washing to obtain a crude PR122 product; and purifying the crude PR122 product. According to the method, hydrogen peroxide is adopted to replace a traditional oxidizing agent, and an oxidation process is optimized, so the purpose of improving product yield is achieved.

QUINACRIDONE SOLID SOLUTION PIGMENT, PIGMENT COLORANT, INKJET INK, AND METHOD OF PRODUCING SOLID SOLUTION PIGMENT

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Paragraph 0042-0044, (2020/01/23)

PROBLEM TO BE SOLVED: To provide: a quinacridone solid solution pigment which has a new color tone, an excellent pigment characteristic and a novel skeleton; and a pigment colorant and an inkjet ink that employ the same. SOLUTION: A quinacridone solid solution pigment is a solid solution of a compound represented by the specified general formula (1) and a quinacridone represented by the specified general formula (2). Also provided are a method of producing the same, and a colorant and an inkjet ink that contain the solid solution pigment. SELECTED DRAWING: None COPYRIGHT: (C)2020,JPOandINPIT

Preparation method for quinacridone and derivatives of quinacridone

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, (2017/08/29)

The invention relates to the field of synthesis of organic pigments and discloses a preparation method for quinacridone and derivatives of the quinacridone. The preparation method comprises the steps that dimethyl succinate generates sodium dimethyl succinylsuccinate (DMSS) through cyclic condensation under an effect of sodium methoxide, and then being acidized into DMSS; condensation reaction occurs between the DMSS and aniline or substituted aniline, an intermediate product generated during condensation is directly oxidized and dehydrogenated by sodium 3-nitrobenzene sulfonate to obtain an oxidative product; and finally coarse products of the quinacridone or the derivatives of the quinacridone are prepared from the oxidative product in a ring-closing mode under an effect of polyphosphoric acid, and finally finished products of the quinacridone or the derivatives of the quinacridone are obtained through pigmentation treatment.

METHOD FOR MANUFACTURING DISPERSION OF QUINOLINE DERIVATIVE

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Page/Page column 6, (2009/02/11)

A method for manufacturing a dispersion of a quinoline derivative that is dispersed at a high concentration and has a small particle size. The method includes the steps of preparing a solution by dissolving an N-arylanthranilic acid derivative in an organosulfonic acid, heating the solution and obtaining a reaction liquid in which a quinoline derivative has been produced by a condensation ring-closing reaction, and obtaining a dispersion of the quinoline derivative by mixing the reaction liquid with an aqueous solution. The step of mixing the reaction liquid with an aqueous solution may be performed in a mixing field having a micro-channel.

Quinacridone nanoscale pigment particles

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Page/Page column 21, (2008/12/07)

A nanoscale pigment particle composition includes a quinacridone pigment including at least one functional moiety, and a sterically bulky stabilizer compound including at least one functional group, wherein the functional moiety associates non-covalently with the functional group; and the presence of the associated stabilizer limits the extent of particle growth and aggregation, to afford nanoscale-sized particles.

Quinacridone pigment compositions comprising unsymmetrically substituted components

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Page 15, (2010/02/10)

The present invention relates to a novel quinacridone pigment compositions, a process using a mixed amine synthesis for the ultimate production of the compositions and to their use as colorants for pigmenting high molecular weight organic materials.

PROCESS FOR THE PREPARATION OF ORGANIC PIGMENTS

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Page/Page column 16, (2010/02/14)

The present invention relates to advantageous processes for the manufacture of organic pigments and their precursors. The invention particularly relates to reactions carried out in an "All In One Reactor" (Draiswerke GmbH, Germany), a kneader like the TurbuKneader of the same company, a paddle dryer like the Turbudry of the same company or a related system and thereby submitting the reaction mixtures to enhanced driving power as expressed by a Froude number>1, the reaction mixture being caused to react in high concentrations at elevated temperature.

Organic pigment fine-particle, and method of producing the same

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Page/Page column 29, (2008/06/13)

A method of producing a fine particle of an organic pigment, containing the steps of: flowing a solution of an organic pigment dissolved in an alkaline or acidic aqueous medium, through a channel which provides a laminar flow; and changing a pH of the solution in the course of the laminar flow.

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