EU/US Properties Organoleptics Cosmetics Suppliers Safety Safety in use Safety references References Other Blenders Uses Occurrence Synonyms Articles Notes
 

ci 73900
quino[2,3-b]acridine-7,14-dione, 5,12-dihydro-

Supplier Sponsors

Name:5,12-dihydroquinolino[2,3-b]acridine-7,14-dione
CAS Number: 1047-16-1Picture of molecule3D/inchi
Other(deleted CASRN):39362-27-1
ECHA EINECS - REACH Pre-Reg:213-879-2
FDA UNII: 11P487375P
Nikkaji Web:J8.584G
MDL:MFCD00059956
XlogP3-AA:4.00 (est)
Molecular Weight:312.32804000
Formula:C20 H12 N2 O2
BioActivity Summary:listing
NMR Predictor:Predict (works with chrome, Edge or firefox)
Category:coloring agents (for surface only)
 
US / EU / FDA / JECFA / FEMA / FLAVIS / Scholar / Patent Information:
Google Scholar:Search
Google Books:Search
Google Scholar: with word "volatile"Search
Google Scholar: with word "flavor"Search
Google Scholar: with word "odor"Search
Google Patents:Search
US Patents:Search
EU Patents:Search
Pubchem Patents:Search
PubMed:Search
NCBI:Search
 FDA/DG SANTE Petitions, Reviews, Notices:
FCN 150 Quinacridone red View - notice
FCN 330 Quino(2,3-b)acridine-7,14-dione,5,12-dihydro- View - notice
FDA Mainterm (IAUFC):1047-16-1 ; QUINACRIDONE RED (C.I. PIGMENT VIOLET 19, C.I. NO. 73900)
 
Physical Properties:
Assay: 95.00 to 100.00
Food Chemicals Codex Listed: No
Boiling Point: 568.47 °C. @ 760.00 mm Hg (est)
Flash Point: 430.00 °F. TCC ( 221.30 °C. ) (est)
logP (o/w): 4.291 (est)
Soluble in:
 water, 53.81 mg/L @ 25 °C (est)
 
Organoleptic Properties:
Odor and/or flavor descriptions from others (if found).
 
Cosmetic Information:
CosIng:cosmetic data
Cosmetic Uses: cosmetic colorants
 
Suppliers:
BOC Sciences
For experimental / research use only.
Quinolino[2,3-b]acridine-7,14(5H,12H)-dione
Chemway Chemical
Pigment Violet 19
TCI AMERICA
For experimental / research use only.
Quinacridone >93.0%(N)
 
Safety Information:
Preferred SDS: View
 
Hazards identification
 
Classification of the substance or mixture
GHS Classification in accordance with 29 CFR 1910 (OSHA HCS)
None found.
GHS Label elements, including precautionary statements
 
Pictogram
 
Hazard statement(s)
None found.
Precautionary statement(s)
None found.
Oral/Parenteral Toxicity:
oral-rat LD50 > 20 mL/kg
BEHAVIORAL: SOMNOLENCE (GENERAL DEPRESSED ACTIVITY) GASTROINTESTINAL: "HYPERMOTILITY, DIARRHEA"
National Technical Information Service. Vol. OTS0533794

Dermal Toxicity:
skin-rabbit LD > 2 mL/kg
National Technical Information Service. Vol. OTS0533795

Inhalation Toxicity:
Not determined
 
Safety in Use Information:
Category:
coloring agents (for surface only)
Recommendation for ci 73900 usage levels up to:
 not for fragrance use.
 
Recommendation for ci 73900 flavor usage levels up to:
 not for flavor use.
 
Safety References:
EPI System: View
AIDS Citations:Search
Cancer Citations:Search
Toxicology Citations:Search
EPA Substance Registry Services (TSCA):1047-16-1
EPA ACToR:Toxicology Data
EPA Substance Registry Services (SRS):Registry
Laboratory Chemical Safety Summary :13976
National Institute of Allergy and Infectious Diseases:Data
WGK Germany:1
5,12-dihydroquinolino[2,3-b]acridine-7,14-dione
Chemidplus:0001047161
RTECS:VA8533500 for cas# 1047-16-1
 
References:
 5,12-dihydroquinolino[2,3-b]acridine-7,14-dione
NIST Chemistry WebBook:Search Inchi
Canada Domestic Sub. List:1047-16-1
Pubchem (cid):13976
Pubchem (sid):134981427
 
Other Information:
(IUPAC):Atomic Weights of the Elements 2011 (pdf)
Videos:The Periodic Table of Videos
tgsc:Atomic Weights use for this web site
(IUPAC):Periodic Table of the Elements
FDA Indirect Additives used in Food Contact Substances:View
HMDB (The Human Metabolome Database):HMDB34058
FooDB:FDB012304
Export Tariff Code:2933.99.9700
FDA Color Additive Status ListView
ChemSpider:View
Wikipedia:View
 
Potential Blenders and core components note
None Found
 
Potential Uses:
 cosmetic colorants
 hair dyeing agents
 
Occurrence (nature, food, other):note
 not found in nature
 
Synonyms:
 c.i. 73900
 C.I. pigment violet 19
 CI pigment violet 19
 cinquasia red
 cinquasia red Y
 cinquasia violet
5,12-dihydro-quino(2,3-b)acridine-7,14-dione
5,12-dihydroquino(2,3-b)acridine-7,14-dione
5,12-dihydroquino[2,3-b]acridine-7,14-dione
5,12-dihydroquinolino[2,3-b]acridine-7,14-dione
 fastogen super red BN
 hostaperm red E5B
 hostaperm red violet ER
 monastral red
 monastral red Y
 monastral violet R
 monastrol red Y
 paliogen red BG
 permanent red E3B
 pigment pink quinacridone S
 pigment violet #19
 pigment violet 19
 pigment violet 19 (c.i. 73900)
 pigment violet quinacridone
 PV fast red E3B
 quinacridone
 quinacridone red
 quinacridone violet
 quino(2,3,b)acridine-7,14-dione, 5,12-dihydro-
 quino[2,3-b]acridine-7,14-dione, 5,12-dihydro-
 sunfast red 19
 sunfast violet
 

Articles:

PubMed:Solution-Processable Core-Extended Quinacridone Derivatives with Intact Hydrogen Bonds.
PubMed:Spectroelectrochemical Studies on Quinacridone by Using Poly(vinyl alcohol) Coating as Protection Layer.
PubMed:Total-scattering pair-distribution function of organic material from powder electron diffraction data.
PubMed:Pigment violet 19 - a test case to define a simple method to simulate the vibronic structure of absorption spectra of organic pigments and dyes in solution.
PubMed:Azo pigments and quinacridones induce delayed hypersensitivity in red tattoos.
PubMed:Dynamic behavior, electrochromism, and two-photon absorption of dicyanomethylenated quinacridone.
PubMed:Hydrogen-bonded organic semiconductor micro- and nanocrystals: from colloidal syntheses to (opto-)electronic devices.
PubMed:Quinacridone on Ag(111): Hydrogen Bonding versus Chirality.
PubMed:Direct electrochemical capture and release of carbon dioxide using an industrial organic pigment: quinacridone.
PubMed:Adsorption study and detection of the high performance organic pigments quinacridone and 2,9-dimethylquinacridone on Ag nanoparticles by surface-enhanced optical spectroscopy.
PubMed:Green-sensitive organic photodetectors with high sensitivity and spectral selectivity using subphthalocyanine derivatives.
PubMed:Electrochemical SERS study on a copper electrode of the insoluble organic pigment quinacridone quinone using ionic liquids (BMIMCl and TBAN) as dispersing agents.
PubMed:Monitoring eukaryotic and bacterial UDG repair activity with DNA-multifluorophore sensors.
PubMed:Hydrogen-bonded semiconducting pigments for air-stable field-effect transistors.
PubMed:Silica cross-linked nanoparticles encapsulating fluorescent conjugated dyes for energy transfer-based white light emission and porphyrin sensing.
PubMed:Tuning structural and mechanical properties of two-dimensional molecular crystals: the roles of carbon side chains.
PubMed:π-π interaction of quinacridone derivatives.
PubMed:High-resolution triple-color patterns based on the liquid behavior of organic molecules.
PubMed:Fabrication of the smallest organic nanocolloids by a top-down method based on laser ablation.
PubMed:Homogeneous epitaxial growth of N,N'-di(n-butyl)quinacridone thin films on Ag(110).
PubMed:Solution SERS of an insoluble synthetic organic pigment-quinacridone quinone-employing calixarenes as dispersive cavitands.
PubMed:Electron injection barrier reduction for organic light-emitting devices by quinacridone derivatives.
PubMed:Quinacridone-based molecular donors for solution processed bulk-heterojunction organic solar cells.
PubMed:Ultraviolet-visible absorption and luminescence properties of quinacridone-barium sulfate solid mixtures.
PubMed:Novel urea-functionalized quinacridone derivatives: ultrasound and thermo effects on supramolecular organogels.
PubMed:Direct observation of enantiospecific substitution in a two-dimensional chiral phase transition.
PubMed:Tunable multicolor ordered patterns with two dye molecules.
PubMed:Homochiral recognition among organic molecules on copper(110).
PubMed:Sonication-induced molecular gels based on mono-cholesterol substituted quinacridone derivatives.
PubMed:Site-isolated, intermolecularly photocrosslinkable and patternable dendritic quinacridones.
PubMed:UV-Vis absorption and photoluminescence characteristics of doped organic solid depend on its doping concentration.
PubMed:Alkyl chain length dependent morphology and emission properties of the organic micromaterials based on fluorinated quinacridone derivatives.
PubMed:Color tuning via adjusting the dye-loading capacity of a polymer.
PubMed:Laser fabrication and spectroscopy of organic nanoparticles.
PubMed:1H NMR study on the self-association of quinacridone derivatives in solution.
PubMed:Theoretical analysis of the intermolecular interaction effects on the excitation energy of organic pigments: solid state quinacridone.
PubMed:Rietveld refinement of a wrong crystal structure.
PubMed:Supramolecular self-assembly initiated by solid-solid wetting.
PubMed:Alkyl and dendron substituted quinacridones: synthesis, structures, and luminescent properties.
PubMed:Crystal structure prediction of organic pigments: quinacridone as an example.
PubMed:STM study on 2D molecular assemblies of luminescent quinacridone derivatives: structure fine-tuned by introducing bulky substitutes and co-adsorption with monofunctional/bifunctional acid.
PubMed:Solution and solid-state spectra of quinacridone derivatives as viewed from the intermolecular hydrogen bond.
PubMed:The pi-pi stacked geometries and association thermodynamics of quinacridone derivatives studied by 1H NMR.
PubMed:Prospective evaluation of the oxygen uptake efficiency slope as a submaximal predictor of peak oxygen uptake in aged patients with ischemic heart disease.
PubMed:Supramolecular structures and assembly and luminescent properties of quinacridone derivatives.
PubMed:Role of lateral alkyl chains in modulation of molecular structures on metal surfaces.
PubMed:Disodium 2,5-bis(phenylamino)terephthalate decahydrate, an intermediate in the industrial synthesis of quinacridone pigments.
PubMed:Preferential interactions in pigmented, polymer blends - C.I. Pigment Blue 15:4 and C.I. Pigment Red 122 - as used in a poly(carbonate)-poly(butylene terephthalate) polymer blend.
PubMed:STM study on quinacridone derivative assemblies: modulation of the two-dimensional structure by coadsorption with dicarboxylic acids.
PubMed:Dendritic incorporation of quinacridone: solubility, aggregation, electrochemistry, and solid-state luminescence.
PubMed:Acridones and quinacridones: novel fluorophores for fluorescence lifetime studies.
PubMed:Contact dermatitis from red tattoo pigment (quinacridone) with secondary spread.
PubMed:Monodispersed quinacridone nanocrystals prepared by a high-temperature and high-pressure liquid crystallization method.
PubMed:Early stages of particle formation in precipitation reactions-quinacridone and boehmite as generic examples.
PubMed:Inflammatory reactions from organic pigments in red tattoos.
PubMed:Effects of host hormonal status on binding of activated estrogen receptor to nuclei from R3230AC and 7,12-dimethylbenz[a]anthracene-induced mammary tumors.
PubMed:[Red pigment dyes and acne. Clinical observations and experimental investigations (author's transl)].
 
Notes:
organic dye used in red tattoos. FDA approved colourant for food-contact paper and board packaging Quinacridone is a red powder. It is an organic compound with the molecular formula C20H12N2O2. It is used as a pigment; analogs bearing this motif are known as quinacridones.
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