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Golden Fluid Acrylics - Indian Yellow Historical Hue, 8 oz bottle

Fluid Acrylic

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$30.58

Blick Art Materials · recorded Oct 21, 2026, 8:31 AM UTC

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Product details
Size
237 ml
Blick SKU
00638-4735
About this product range
  • Professional quality
  • Comparable pigment load to Golden Heavy Body Acrylics
  • 100% acrylic emulsion; no fillers, dyes, or opacifiers
  • Intense, permanent colors with a smooth, fluid consistency
  • Excellent lightfastness
  • Made in the USA

Golden Fluid Acrylics deliver strong, permanent color in a creamy, pourable consistency that artists love. Formulated with pure lightfast pigments and no added fillers or extenders, these paints offer the same pigment load as Golden’s Heavy Body line—but with a smooth, fluid flow perfect for a wide range of techniques.

Enjoy vibrant color and fine dispersion whether you’re brushing, spraying, staining, or blending with other Golden products. Fluid Acrylics mix easily with mediums for custom effects and adhere well to canvas, paper, fabric, and more. Flexible and durable when dry, they’re an excellent choice for artists who want maximum color with effortless application.

Pigment information

General reference notes about pigments can describe other media (such as oil). They do not verify this product’s exact formulation or behavior.

Nickel Azo Yellow

Pigment code
PY150
Type
inorganic
Chemical name
nickel azomethine yellow
Chemical formula
C30H18Cl2N6NiO4
Properties
Nickel Azo Yellow is a transparent, moderately staining yellow pigment with high tinting strength. It is considered a good color match in botanical and landscape painting for natural gamboge (NY24), a historic yellow pigment with fair to poor lightfastness.
Permanence
Nickel azomethine yellow has excellent lightfastness.
Toxicity
Nickel azo yellow pigment is mildly toxic, and is often labeled as hazardous. Avoid respiratory and skin exposure to pigment dust. It should be disposed of properly with other hazardous wastes, not washed down the sink.
History
Nickel azomethine yellow has been developed as an artist pigment becasue it is a close match for gamboge, a historic yellow.
Description
Gamboge Hue, New Gamboge.

Benzimidazolone Yellow

Pigment code
PY154
Type
monoazo
Properties
Benzimidazolone Yellow is a pigment with dull tints and an average drying time.
Permanence
Benzimidazolone Yellow has excellent lightfastness.
Toxicity
Benzimidazolone Yellow is not considered toxic.
History
The benzimidazolone group of pigments was developed and patented in 1960 by Hoechst A.G., a German chemical manufacturer that was a forerunner of the pharmaceutical company Aventis.
Description
Benzimidazolone.

Quinacridone Magenta

Pigment code
PR122
Type
organic, quinacridone
Chemical formula
C22H16N2O2
Properties
Quinacridone Magenta is a semi-transparent and powerful bluish red with an impressive mixing range. It makes an excellent glazing color and is one of the bluest of the Quinacridone colors. The pigment's properties vary considerably, depending on how it is ground. Quinacridone pigments have relatively low tinting strength in general. For this reason, quinacridone colors are often expensive, because more pigment is required in the formulation.
Permanence
Quinacridone Magenta offers very good lightfastness in most media, but some have argued that it is less lightfast in watercolor form. Although Quinacridone Magenta received only a passing grade of "fair" under ASTM test protocols, other test results have rated the pigment very good to excellent. Transparent reddish violet pigments in general have more problems with lightfastness than any other range of colors. PR122 is often used as the Magenta of CMYK (four color) process printing because it offers a better tradeoff between tinting strength and lightfastness than other pigments in its class.
Toxicity
Quinacridone Magenta has no acute hazards. Overexposure to quinacridone pigments may cause skin irritation. Quinicridone pigments contain a compound found to be a skin, eye, and respiratory irritant.
History
Quinacridone Magenta came from a red violet aniline dye that was first produced in 1858 by Natanson. It was called Magenta to commemorate a battle in Magenta, Italy. Over time, Magenta became the standard color name for a deep, violet red. Although quinacridone compounds became known in the late 19th century, methods of manufacturing so as to make them practical for use as commercial pigments did not begin until the 1950s. PR122 has become particularly popular in the formulation of Magenta for CMYK process printing.
Description
Acra Red, Quinacridone Violet (PV19), Thalo Red Rose.

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