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234133

Sigma-Aldrich

Quinoline Yellow

Dye content 95 %

Synonyme(s) :

Solvent yellow 33

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About This Item

Formule empirique (notation de Hill):
C18H11NO2
Numéro CAS:
8003-22-3
Poids moléculaire :
273.29
Numéro C.I. (Colour Index):
47000
Numéro CE :
232-318-2
Numéro MDL:
MFCD00011593
Code UNSPSC :
12171500
ID de substance PubChem :
24854023
Nomenclature NACRES :
NA.47

Description

spirit soluble

Niveau de qualité

100

Pureté

≥95% (HPLC)

Forme

powder

Composition

Dye content, 95%

Technique(s)

titration: suitable

Pf

240 °C

Solubilité

chloroform: 1 mg/mL, clear to slightly hazy, yellow to very deep yellow

λmax

439 nm

Amax

1.16 at 285-291 nm in methanol at 0.01 g/L

Application(s)

diagnostic assay manufacturing
hematology
histology

Température de stockage

room temp

Chaîne SMILES 

O=C1C(c2ccc3ccccc3n2)C(=O)c4ccccc14

InChI

1S/C18H11NO2/c20-17-12-6-2-3-7-13(12)18(21)16(17)15-10-9-11-5-1-4-8-14(11)19-15/h1-10,16H

Clé InChI

IZMJMCDDWKSTTK-UHFFFAOYSA-N

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Description générale

Quinoline Yellow belongs to the class of quinophthalone dyes. It is generally used as a food colorant. Quinoline Yellow is anionic in nature and is used to dye wool and silk. Studies show that Quinoline Yellow is not genotoxic or carcinogenic. It is considered to be safe for human health.

Pictogrammes

Exclamation mark
GHS07

Mention d'avertissement

Warning

Mentions de danger

H315,H319,H335

Classification des risques

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Organes cibles

Respiratory system

Code de la classe de stockage

11 - Combustible Solids

Classe de danger pour l'eau (WGK)

WGK 2

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable

Équipement de protection individuelle

Eyeshields, Gloves, type ABEK (EN14387) respirator filter

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Certificats d'analyse (COA)

Lot/Batch Number
SHBN4586
SHBL1993
SHBL0148
MKCH9214
MKCG4048

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Michael Saltmarsh, Mike Saltmarsh
Essential Guide to Food Additives (2013)
B Björkner et al.
Contact dermatitis, 7(1), 1-4 (1981-01-01)
The quinoline color D & C Yellow No. 11 was added to a standard test series. Of 88 patients tested with 1% in PEG, four showed unexplained positive test reactions. One patient had a "flare-up" reaction after 14 days. At
S M el Dareer et al.
Journal of toxicology and environmental health, 23(3), 385-393 (1988-01-01)
The disposition of 2-(2-quinolyl)-1,3-indandione (D. C. yellow #11, DCY) in male Fischer rats dosed intravenously or by feeding was determined. For rats given [14C]DCY in the feed (0.00044-0.41% of the diet), recovery of radioactivity during the 24-h dosing period and
Ivona Lhotská et al.
Molecules (Basel, Switzerland), 23(12) (2018-12-19)
Food analysis demands fast methods for routine control and high throughput of samples. Chromatographic separation enables simultaneous determination of numerous compounds in complex matrices, several approaches increasing separation efficiency and speed of analysis were involved. In this work, modern types
Kristina Knutson et al.
Biotechnology progress, 20(6), 1893-1896 (2004-12-04)
A laccase-mediator system (LMS) for biobleaching was applied to a bleached chemical pulp dyed with stilbene dye Direct Yellow 11. Of mediators tested, 2,2'-azinobis(3-ethylbenzthiazoline-6-sulfonate) (ABTS) was found to be more effective than either violuric acid (VA) or N-hydroxybenzotriazole (HBT), which
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