<?xml version="1.0" encoding="utf-8"?><metadata xmlns:dc="http://purl.org/dc/elements/1.1/"  xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:dcterms="http://purl.org/dc/terms/"><dc:title xml:lang="en">phthalocyanine blue</dc:title><dc:identifier>http://AATesaurus.cultura.gencat.cat/aat/getty_en?tema=31437393</dc:identifier><dc:language>en</dc:language><dc:publisher xml:lang="en">Getty Institute</dc:publisher><dcterms:created>2026-03-30 20:57:56</dcterms:created><dcterms:isPartOf xsi:type="dcterms:URI">http://AATesaurus.cultura.gencat.cat/aat/getty_en</dcterms:isPartOf><dcterms:isPartOf xml:lang="en">Tesaurus d&apos;Art i Arquitectura</dcterms:isPartOf><dc:format>text/html</dc:format> <dcterms:alternative xml:lang="en">Thalo blue (TM)</dcterms:alternative> <dcterms:alternative xml:lang="en">bleu héliogène</dcterms:alternative> <dcterms:alternative xml:lang="en">phthalo blue</dcterms:alternative> <dcterms:alternative xml:lang="en">Monastral blue</dcterms:alternative> <dcterms:alternative xml:lang="en">Monastral fast blue</dcterms:alternative> <dc:description xml:lang="en"><![CDATA[ Synthetic organic colorant composed of copper phthalocyanine that was first synthesized in 1933; it was marketed as a paint pigment called Monastral blue. The organic colorant is usually adsorbed on an aluminum hydrate base to form a deep blue color. In industry, phthalocyanine blue has replaced all other blue pigments for use in coatings because it is lightfast as well as resistant to chemicals and clumping. ]]></dc:description></metadata>