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Official EU label nameGlossary entry 21039

PIGMENT VIOLET 19

This record confirms an official common ingredient name for EU cosmetic product labelling. It does not by itself confirm that the substance is permitted, unrestricted or safe.

Global evidence snapshot

The resolved identity has matching regulatory evidence in 0 of 13 indexed market datasets: 0 country records and 0 EU Annex records. Every result and evidence gap is listed below.

0 markets with evidence
Markets checked
13
Markets with evidence
0
Evidence gaps
13
Resolved identifiers
2

Resolved substance identity

CAS:1047-16-1
EC:213-879-2
Ingredient index records:
PIGMENT VIOLET 19
Cosmetic functions: HAIR DYEING

5,12-Dihydroquino[2,3-b]acridine-7,14-dione (CI 73900)

Inventory restriction note: II/1366

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1 matched or reported name
PIGMENT VIOLET 19

Regulatory evidence across markets

None of the 13 markets tracked here holds an imported rule under the name PIGMENT VIOLET 19.

That is a statement about this inventory, not about the law: no imported rule is not evidence that a substance is permitted. A rule may exist under a different name, under a CAS or EC number this glossary entry does not carry, or in a dataset not yet imported.

Check the markets and their sourcesSearch every market for this name

Chemical identity and properties

PubChem 2D chemical structure for CAS 1047-16-1
CAS 1047-16-1PubChem CID 13976

Quinacridone

Quinacridone is an organonitrogen heterocyclic compound and an organic heterotetracyclic compound. — ChEBI

IUPAC name
5,12-dihydroquinolino[2,3-b]acridine-7,14-dione
Molecular formula
C20H12N2O2
Molecular weight
312.3 g/mol
Exact mass
312.089877630 Da
XLogP3
4.0
Topological polar surface area
58.2 Ų
Hydrogen-bond donors
2
Hydrogen-bond acceptors
4
Covalent units
1
Defined stereocentres
0

Also known as

CINQUASIA REDMonastral RedQuinacridone violetMonastral Violet RSunfast VioletCinquasia Red BCinquasia Red YMonastral Red B
16 more reported names
Monastral Red YMonastrol Red YPermanent MagentaPaliogen Red BGCinquasia Violet RDark violetSunfast Red 19Cinquasia VioletQuinacridone RedQuinacridone Red MCPermanent Red E 3BQuinacridone Violet MCPV Fast Red E 3BPV Fast Red E 5BHostaperm Red Violet ERHostaperm Red E 3B
Open full PubChem recordPubChem annotations3D structure image
External database identifiers

Evidence from additional scientific databases

EMBL-EBI ChEBI
Exact identifier matchCHEBI:174977

Quinacridone

Formula
C20H12N2O2
Average mass
312.328 g/mol
Monoisotopic mass
312.08988 Da
Formal charge
0
  • organonitrogen heterocyclic compound — is a (CHEBI:38101)
  • organic heterotetracyclic compound — is a (CHEBI:38163)
  • organonitrogen heterocyclic compound — is a (CHEBI:38101)
  • organic heterotetracyclic compound — is a (CHEBI:38163)
Additional curated names
5,12-dihydroquinolino[2,3-b]acridine-7,14-dione
Cross-references from this source

Mapped by: Exact CAS cross-reference in the ChEBI compound record. Retrieved: 2026-08-31. Open source record

NIH PubChem PUG-View
Exact identifier match13976

Attributed physical-property, hazard, environmental and use annotations.

  • Note: This chemical does not meet GHS hazard criteria for 99.6% (760 of 763) of all reports. Source: European Chemicals Agency (ECHA)
  • GHS Hazard Statements: Not Classified; Reported as not meeting GHS hazard criteria by 760 of 763 companies (only 0.4% companies provided GHS information). For more detailed information, please visit ECHA C&L website. Source: European Chemicals Agency (ECHA)
  • ECHA C&L Notifications Summary: Aggregated GHS information provided per 763 reports by companies from 4 notifications to the ECHA C&L Inventory.; Reported as not meeting GHS hazard criteria per 760 of 763 reports by companies.; There are 2 notifications provided by 3 of 763 reports by companies with hazard statement code(s).; Information may vary between notifications depending on impurities, additives, and other factors. The percentage value in parenthesis indicates the notified classification ratio from companies that provide hazard codes. Only hazard codes with percentage values above 10% are shown. For more detailed information, please visit ECHA C&L website. Source: European Chemicals Agency (ECHA)
  • Environmental Bioconcentration: Cinquasia red should not bioconcentrate, since it is insoluble, and therefore, will not be taken up into the body. Source: Hazardous Substances Data Bank (HSDB)

Mapped by: Existing checksum-valid CAS to unique PubChem CID match. Retrieved: 2026-08-31. Open source record

Scientific classifications and hazard annotations provide context and do not replace the market-specific regulatory decision shown above.

Additional source coverage and match status
SourceResultChecked
EMBL-EBI ChEBIExact match2026-08-31
NIH PubChem PUG-ViewExact match2026-08-31

A recorded no-match is useful evidence that the source was checked; it is not a claim that the substance does not exist elsewhere.

Retrieved from NIH PubChem on 2026-08-31 by checksum-valid CAS matching. Chemical properties do not replace the regulatory decision on this page.

Additional authoritative substance research

Each link searches that source for this identity. A link is a research route, not a claim that the source holds an exact record. What each source is, and its legal weight

Cosmetic Ingredient Review safety assessmentsFDA Global Substance Registration SystemILO/WHO International Chemical Safety CardsJapan NITE-CHRIPNIOSH Pocket Guide to Chemical HazardsOECD eChemPortalUS EPA CompTox CTX APIs

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Official source and scope

Imported from Commission Implementing Decision (EU) 2025/1175 (dataset version EU 2025/1175). The glossary supplies common ingredient names for the ingredient list required by Article 19(1)(g); it is not an approval or safety list.

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