Winsor & Newton Griffin Alkyds - Vermilion Hue, 37 ml tube

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Item #:00501-3424
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Winsor & Newton Griffin Alkyd - Vermilion Hue, 37 ml tube and swatch

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CL Cautionary Label

Products bearing the CL seal of the Art & Creative Materials Institute ("Caution Label") contain ingredients that are toxic or hazardous, but when used in properly supervised and controlled conditions, they can be enjoyed with complete safety.

Product Details

Color:
Vermilion Hue
Size:
37 ml
No.
680
Series:
1
Mfg #:
1914680

Colors on Monitors -

Due to differences in users’ monitors, the colors presented are an approximation of the true color.
Shipping Note - Due to manufacturer distribution restrictions, Winsor & Newton products cannot be shipped to addresses outside of North America.

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Pigment Information

This color contains the following pigments:

PR170-Naphthol Red

PW6-Titanium White

PO36-Benzimidazolone Orange


Pigment Name

PR170-Naphthol Red

Pigment Type

organic, naphthol AS

Chemical Formula

C26H22N4O4

Properties

Pigment PR170 is a bright deep red with bluish undertones. It has an average drying time. It has two crystaline forms that differ significantly in opacity. The more transparent form (F5RK) tends to be more bluish and is less lightfast.

Permanence

The lightfastness and weatherfastness of Pigment PR170 varies, depending on the application and the crystaline form. The opaque form (F3RK) has very good lightfastness, and is more weather resistant. The transparent form (F5RK) has lightfastness that is considered acceptable in pure applications, but it fades more in tints. Neither form is considered suitable for exterior use.

Toxicity

Naphthol Reds are not considered toxic. They may cause eye, skin, or respiratory irritation. Contact with dry pigment should be avoided.

History

Naphthol pigments are actually dyes that are "laked" to form pigments. First developed by the German chemical company Hoechst A.G. before World War I, their use in artist paints began in the 1920s. Pigment Red PR170 is a Naphthol AS pigment, chemically related to the diarylide yellow pigments. The Naphthol AS pigments comprise a range of reds. They are used in plastics, textiles, and printing inks.


Pigment Name

PW6-Titanium White

Pigment Type

inorganic

Chemical Name

titanium dioxide

Chemical Formula

TiO2

Properties

Titanium White is the most brilliant of the white pigments. It is considered an all purpose oil color useful in all techniques and the best all around white. Its masstone is neither warm nor cool, placing it somewhere between Lead White and Zinc White. It is less prone to cracking and yellowing than Lead White, but it still yellows easily. Titanium White dries slowly in oil form, more slowly than Lead White but more quickly than Zinc White. It is opaque in oil and acrylic forms and semi-opaque in watercolor form. This pigment has good chemical stability, and its tinting strength is superior to both Lead White and Zinc White.

Permanence

Titanium White has excellent permanence and lightfastness.

Toxicity

Titanium dioxide is highly stable and is regarded as non-toxic.

History

Titanium is the ninth most abundant element in the Earth's crust, however mineral deposits that are economical to mine are less common. Titanium dioxide was first discovered in 1821, although it could not be mass produced until 1919. Widespread use of the pigment began in the 1940s. Since that time, it has become the most commonly used white pigment. The name comes from the Latin word Titan, the name for the elder brother of Kronos and ancestor of the Titans, and from the Greek word tito, meaning day or sun.


Pigment Name

PO36-Benzimidazolone Orange

Pigment Type

organic, monoazo

Chemical Formula

C17H13ClN6O5

Properties

Benzimidazolone Orange is a reddish orange pigment that can lose its intensity and become dull in tints. It has an average drying time.

Permanence

Benzimidazolone Orange has excellent lightfastness and outstanding heat and solvent stability for a monoazo pigment.

Toxicity

Benzimidazolone Orange 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. Use of benzimidazolone pigments in the auto industry, especially Benzimidazolone Orange, became common in the 1980s because they were common replacements for lead chromate pigments, which were phased out during this period.


Safety Data Sheet

UPC Code: 094376916911

ASIN #: B007NLRGQA