Holbein Duo Aqua Water Soluble Oils - Olive Green, 40 ml tube

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Item #:00494-7073
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Holbein Duo Aqua Water Soluble Oil - Olive Green, 40 ml tube and swatch

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AP Non-Toxic

Products bearing the AP seal of the Art & Creative Materials Institute, Inc. (ACMI) are certified non-toxic. A product can be certified non-toxic only if it contains no materials in sufficient quantities to be toxic or injurious to humans, or to cause acute or chronic health problems when used as intended. See [Health and Safety ](https://www.dickblick.com/learning-resources/product-info/health-safety/ "Learning-resources/product-info/health-safety")for further information.

Product Details

No.
251
Description:
Duo Aqua Oil Paint
Color:
Olive Green
Size:
40 ml (1.35 oz)
Format:
Tube
Series:
C

Colors on Monitors -

Due to differences in users’ monitors, the colors presented are an approximation of the true color.

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Pigment Information

This color contains the following pigments:

PG8-Hooker’s Green

PB29-Ultramarine [Blue]

PR83-Alizarin Crimson

PY95-Disazo Condensation Yellow


Pigment Name

PG8-Hooker’s Green

Pigment Type

mix of organic pigments

Chemical Formula

C30H18FeN3O6Na

Properties

Hooker’s Green is a bright olive-green often sold in a yellowish shade and a bluish shade. Its transparency can range from dull and dark to bright and light because lightness and chroma vary based on manufacturer. Modern varieties have a rich, dark tone that provides a great range when mixing. Hooker’s Green is particularly good for landscape painting when a larger range of foliage is required. Dioxazine Violet is the best mixing compliment in watercolor form.

Permanence

The permanence and lightfastness of Hooker’s Green varies by brand. As a composite pigment historically mixed from Prussian Blue and Gamboge, its permanence is only fair. Modern replacements for Hooker's Green tend to be mixed with components that have more permanence, such as Phthalocyanine Green, Burnt Umber, and sometimes Hansa or Cobalt Yellow.

Toxicity

Hooker’s Green can be hazardous, but the toxicity level depends on the specific pigments used by each individual manufacturer or brand.

History

This pigment was originally an unreliable mix of Prussian or Iron Blue and Gamboge. Later, it became a more reliable mix of Cadmium Yellow and Phthalo Blue or Green. It was a staple green for 19th century landscape and botanical painters. Most modern Hooker’s Green paints are yellow greens with a hue angle around 140, or a mix of Phthalo Green and Burnt Umber.


Pigment Name

PB29-Ultramarine [Blue]

Pigment Type

inorganic

Chemical Name

complex silicate of sodium and aluminum with sulfur

Chemical Formula

Na8-10Al6Si6O24S2-4 or Na6-8Al6Si6O24S2-4

Properties

Ultramarine is the standard warm blue, a brilliant blue pigment that has the most purple and least green in its undertone. It has a moderate to high tinting strength and a beautiful transparency. Synthetic Ultramarine is not as vivid a blue as natural Ultramarine. Ultramarine dries slowly in oil and tends to produce clean, though granular, washes in watercolor. French Ultramarine mixes well with Alizarin colors in oil and watercolor form to create a range of purples and violets. It can dull when mixed with white in acrylic form, but mixes well with other colors. The shade varies based on manufacturer. Considered a great color for glazes, it is not suitable for frescoing.

Permanence

Ultramarine has excellent permanence, although synthetic Ultramarine is not as permanent as natural Ultramarine. It may discolor if exposed to acid because of its sulfuric content.

Toxicity

Ultramarine has no significant hazards.

History

The name for this pigment comes from the Middle Latin ultra, meaning beyond, and mare, meaning sea, because it was imported from Asia to Europe by sea. It is a prominent component of lapis lazuli and was used on Asian temples starting in the 6th century. It was one of the most expensive pigments in 16th century Europe, worth twice its weight in gold, and so was used sparingly and when commissions were larger. Ultramarine is currently imitated by a process invented in France in 1826 by Jean Baptiste Guimet, making blue affordable to artists and extending the range of colors on their palettes.


Pigment Name

PR83-Alizarin Crimson

Pigment Type

organic

Chemical Name

1,2-dihydroxyantraquinone

Chemical Formula

C14H8O4

Properties

Alizarin Crimson, the traditional cool counterpart to Cadmium Red, is a clear ruby-red with a maroon masstone and a bluish undertone. It is the artist's principal deep red pigment, is transparent, and has good tinting strength. It creates bright rosy pinks when mixed with white, a range of purples and violets when mixed with strong blues, can be slow drying when used with oils, and is compatible with all other pigments. Permanent Alizarin Crimson mixes well with Ultramarine in acrylic and watercolor form. Permanent Rose and Quinacridone Rose are possible alternatives on a watercolor palette. Alizarin Crimson is a popular glazing color.

Permanence

Alizarin Crimson is considered fugitive or marginally lightfast, and the appropriateness of its use in the modern artist palette is a subject of debate. There are many concerns regarding its permanence, particularly when mixed with ochre, sienna, and umber, or when used thinly. It is the least permanent red commonly used by today's artists. Modern synthetic preparations of Alizarin Crimson have better permanence and lightfastness that the original natural pigment, which was extracted from the madder plant. Quinacridone pigments have been used to create a modern hue that closely matches the original hue, but many artists object that the transparency and handling characteristics are not the same as for the original.

Toxicity

Alizarin Crimson can be slightly toxic if it comes into contact with skin and may cause some allergies. There is no significant acute toxicity.

History

The word alizarin comes from the Arabic word al-usara, meaning juice. The base ingredient of this pigment is the Madder plant (Rubia Tinctorum). It was used for dyes and inks among craftsmen in Ancient Persia, India, and Egypt as early as 1500 BC In 1804, George Field, an English dye maker, developed Madder Lake by binding madder to alum, a white powder. The German chemists Carl Grabe and Carl Liebermann produced the first synthetic variety of this pigment, most commonly known as Alizarin Crimson, in 1868. They used anthracene, which greatly improved the lightfastness. The Colour Index International designation PR83:1 has been used to identify this synthetic laked pigment.


Pigment Name

PY95-Disazo Condensation Yellow

Pigment Type

organic, disazo condensation

Properties

Pigment PY95 is a semi-transparent reddish yellow pigment with high tinting strength, slightly less reddish in hue than the popular PY83.

Permanence

For a yellow organic pigment, Disazo Condensation Yellow 95 has very good lightfastness, although its lightfastness is not as good as that of red disazo condensation pigments.

Toxicity

Disazo Condensation Yellow has no significant acute hazards. Chronic hazards have not been well studied.

History

Disazo Condensation Yellow PY95 is sometimes used in yellow inkjet printer inks and other high-grade, special purpose inks.


Safety Data Sheet

UPC Code: 4900669232513

ASIN #: B0008ENPFU