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309052

Sigma-Aldrich

Quinoline Yellow

Mixture of the mono- and disulfonic acids of Quinoline Yellow

Synonym(s):

Acid Yellow 3

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About This Item

CAS Number:
Colour Index Number:
47005
UNSPSC Code:
12171500
NACRES:
NA.47

Quality Level

form

powder

technique(s)

titration: suitable

solubility

H2O: soluble
spirit: soluble (23,413-3)

λmax

412 nm

application(s)

diagnostic assay manufacturing
hematology
histology

storage temp.

room temp

InChI

1S/C18H11NO8S2.2Na/c20-17-11-3-1-2-4-12(11)18(21)15(17)13-6-5-9-7-10(28(22,23)24)8-14(16(9)19-13)29(25,26)27;;/h1-8,15H,(H,22,23,24)(H,25,26,27);;/q;2*+1/p-2

InChI key

FZUOVNMHEAPVBW-UHFFFAOYSA-L

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General description

Quinoline Yellow is a yellow, water-soluble, anionic quinophthalone dye. This synthetic dye is generally used as a food additive. Its applications are also seen in the cosmetic and pharmaceutical industries. It is a chinophthalon derivative applied in the compositions of skin, lips, or body cosmetics.Studies show that Quinoline Yellow is not genotoxic or carcinogenic. It is considered to be safe for human health.

Application

Quinoline Yellow has been used as an absorber for the fabrication of the micro-phantoms.

Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

Precautionary Statements

Hazard Classifications

Acute Tox. 4 Oral

Storage Class Code

11 - Combustible Solids

WGK

WGK 1

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Adrian Weisz et al.
Journal of mass spectrometry : JMS, 37(10), 1025-1033 (2002-10-11)
Several positional isomers of 2-(2-quinolinyl)-1H-indene-1,3(2H)-dione mono- and disulfonic acids prepared as reference materials for development of analytical methods involved in FDA certification of D&C Yellow No. 10 (Quinoline Yellow) were found consistently to show [MH + 14](+) ions when their
Hisao Oka et al.
Journal of chromatography. A, 989(2), 249-255 (2003-03-26)
Quinoline yellow (Color Index No. 47005) consists of multiple components that show a large difference in their partition coefficients (K), ranging from 0.03 to 3.3 in the solvent system tert.-butyl methyl ether (MTBE)-1-butanol-acetonitrile-aqueous 0.1 M trifluoroacetic acid (TFA). Consequently, it
M Florian et al.
Food additives and contaminants, 19(9), 803-809 (2002-10-25)
A study of the voltammetric behaviour of the food colours brilliant blue FCF (C.I. 42090), erythrosine (C.I. 45430) and quinoline yellow (C.I. 47005) in the pH range 2-10 have been carried out by cathodic#10; stripping voltammetry. At pH 4.5 (acetate
Karen Lau et al.
Toxicological sciences : an official journal of the Society of Toxicology, 90(1), 178-187 (2005-12-15)
Exposure to non-nutritional food additives during the critical development window has been implicated in the induction and severity of behavioral disorders such as attention deficit hyperactivity disorder (ADHD). Although the use of single food additives at their regulated concentrations is
A Weisz et al.
Journal of chromatography. A, 923(1-2), 87-96 (2001-08-21)
The main components of the color additive D&C Yellow No. 10 (Quinoline Yellow, Color Index No. 47005), 2-(2-quinolinyl)-1H-indene-1,3(2H)-dione-6'-sulfonic acid (6SA) and 2-(2-quinolinyl)-1H-indene-1,3(2H)-dione-8'-sulfonic acid (8SA), were isolated from the dye mixture by pH-zone-refining counter-current chromatography (CCC) in the ion-exchange mode. These

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