Naphthol pigments: Difference between revisions

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== Description ==
== Description ==


A broad class of azoic colorants that contain a backbone of 2-hydroxy-3-naphthanilide and include many shades of red, some oranges and a green. In 1911, three German scientists at Naphtol-Chemi Offenbach coupled the acid backbone with aniline and toluidine diazonium salts. The new discovery was patented and sold as under the trade name Napthol AS.  Several intense colors, reds and oranges, were produced and known as Grela Reds.  They had high tinting strength but were laborious to make.  As such, the compounds did not become popular until they were laked into pigments and used in artists paints by IG Farben.  Later, a series of naphthol reds, called American Naphthol Reds, was introduced to the United States in the 1940s (Berrie and Lomax 1997). About 6% of the red colorants used in 1985 were naphthol pigments. They provide good tinting strength and good lightfastness but can bleed when exposed to organic solvents. Naphthol reds are used to color plastics, automotive finishes, architectural paints, pencils, crayon, printing inks and inexpensive artists oil paints and watercolors.
A broad class of azoic colorants that contain a backbone of 2-hydroxy-3-naphthanilide and include many shades of red, some oranges and a green. In 1911, three German scientists at Naphtol-Chemi Offenbach coupled the acid backbone with aniline and toluidine diazonium salts. The new discovery was patented and sold as under the trade name Napthol AS.  Several intense colors, reds and oranges, were produced and known as Grela Reds.  They had high tinting strength and were washfast on cottons, but were laborious to make.  As such, the compounds did not become popular until they were laked into pigments and used in artists paints by IG Farben.  Later, a series of naphthol reds, called American Naphthol Reds, was introduced to the United States in the 1940s (Berrie and Lomax 1997). About 6% of the red colorants used in 1985 were naphthol pigments. They provide good tinting strength and good lightfastness but can bleed when exposed to organic solvents. Naphthol reds are used to color plastics, automotive finishes, architectural paints, pencils, crayon, printing inks and inexpensive artists oil paints and watercolors.


See also [[Beta naphthol pigment]].
See also [[Beta naphthol pigment]].
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== Physical and Chemical Properties ==
== Physical and Chemical Properties ==


Resistant to acid, alkali and soap.
* Resistant to acid, alkali and soap.
* May bleed with some organic solvents
* Generally good to excellent lightfastness


== Resources and Citations ==
== Resources and Citations ==

Revision as of 14:18, 7 March 2026

Description

A broad class of azoic colorants that contain a backbone of 2-hydroxy-3-naphthanilide and include many shades of red, some oranges and a green. In 1911, three German scientists at Naphtol-Chemi Offenbach coupled the acid backbone with aniline and toluidine diazonium salts. The new discovery was patented and sold as under the trade name Napthol AS. Several intense colors, reds and oranges, were produced and known as Grela Reds. They had high tinting strength and were washfast on cottons, but were laborious to make. As such, the compounds did not become popular until they were laked into pigments and used in artists paints by IG Farben. Later, a series of naphthol reds, called American Naphthol Reds, was introduced to the United States in the 1940s (Berrie and Lomax 1997). About 6% of the red colorants used in 1985 were naphthol pigments. They provide good tinting strength and good lightfastness but can bleed when exposed to organic solvents. Naphthol reds are used to color plastics, automotive finishes, architectural paints, pencils, crayon, printing inks and inexpensive artists oil paints and watercolors.

See also Beta naphthol pigment.

Synonyms and Related Terms

naphthol dye; azoic dye; Naphthol Red; Naphthol AS; napthol dye (sp); hydroxynaphthoic anilide; Naphtol Anilid Saure (Deut.); Naphtol AS (Deut.); pigment à base de naphtol (Fr.); Grela Reds

Common Naphthol Pigments


Pigment

Name(s)

Color

Key Properties

Common Applications
PR2 Naphthol Red Light Bluish Red Good lightfastness, poor solvent resistance Industrial paints, printing inks
PR5 Naphthol Red Mid-red Good lightfastness, high color strength Artists' paints, coatings
PR9 Naphthol Red/Scarlet Yellowish Red High lightfastness, good water fastness Textiles, high-grade paints
PR12 Naphthol Red Yellowish Red Good tinting strength, similar to Red Lake C Printing inks, plastics, coatings
PR112 Naphthol Red Medium Warm Red Excellent lightfastness, high hiding power Watercolors, automotive, plastic
PR146 Carmine FBB Bluish Red Very high lightfastness, good heat stability Packaging inks, high-end paints
PR170 Naphthol Red Blue-shade Red Versatile, high tinting strength, good lightfastness Artists' oil/acrylic, automotive
PR184 Naphthol Rubine Bluish Red High strength, low lightfastness Printing inks, metal decorating
PR188 Naphthol Red Mid/Yellowish Excellent solvent and light stability Automotive finishes, inks
PO5 Orthonitroaniline Orange Poor lightfastness and solvent bleed Crayons, paper, inks
PO24 Naphthol Orange Orange Moderate lightfastness, good tinting Inks, plastics
PG12 Naphthol Green Green Iron complex, good lightfastness Industrial, artist paints

Physical and Chemical Properties

  • Resistant to acid, alkali and soap.
  • May bleed with some organic solvents
  • Generally good to excellent lightfastness

Resources and Citations

  • B. Berrie, S.Q. Lomax, 'Azo Pigments: Their History, Synthesis, Properties and Use in Artists' Materials', Studies in the History of Art, National Gallery of Art, Washington DC, No. 57, 1997. Comment: patented 1911
  • Richard S. Lewis, Hawley's Condensed Chemical Dictionary, Van Nostrand Reinhold, New York, 10th ed., 1993. Comment: Napthol AS = azoic coupling component
  • Hoechst Celanese Corporation, Dictionary of Fiber & Textile Technology (older version called Man-made Fiber and Textile Dictionary, 1965), Hoechst Celanese Corporation, Charlotte NC, 1990
  • Rosalie Rosso King, Textile Identification, Conservation, and Preservation, Noyes Publications, Park Ridge, NJ, 1985
  • Fairchild's Dictionary of Textiles, Phyllis G.Tortora, Robert S. Merkel (eds.), Fairchild Publications, New York City, 7th edition, 1996
  • Encyclopedia Britannica, http://www.britannica.com Comment: "Chemical Compound." (Accessed 13 May 2004). gives date of first use as 1912
  • Liquitex: Naphthol Crimson