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Key Documents

11344

Supelco

Disperse Yellow 3

analytical standard

Sinonimo/i:

4-(2-Hydroxy-5-methylphenylazo)acetanilide, N-[4-(2-Hydroxy-5-methylphenylazo)phenyl]acetamide

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About This Item

Formula empirica (notazione di Hill):
C15H15N3O2
Numero CAS:
Peso molecolare:
269.30
Colour Index:
11855
Beilstein:
1915225
Numero CE:
Numero MDL:
Codice UNSPSC:
85151701
ID PubChem:
NACRES:
NA.24

Grado

analytical standard

Livello qualitativo

Saggio

≥96.0% (HPLC)

Durata

limited shelf life, expiry date on the label

tecniche

HPLC: suitable
gas chromatography (GC): suitable

Punto di fusione

268-270 °C (lit.)

applicazioni

cleaning products
cosmetics
environmental
food and beverages
personal care

Formato

neat

Stringa SMILE

CC(=O)Nc1ccc(cc1)N=Nc2cc(C)ccc2O

InChI

1S/C15H15N3O2/c1-10-3-8-15(20)14(9-10)18-17-13-6-4-12(5-7-13)16-11(2)19/h3-9,20H,1-2H3,(H,16,19)
PXOZAFXVEWKXED-UHFFFAOYSA-N

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Descrizione generale

Disperse Yellow 3 is an yellow azo dye which is majorly used in textile industry. It also has carcinogenic properties.

Applicazioni

It was used to understand that Phanerochaete chrysosporium can mineralize azo dyes with radiolabeled substrate.
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Confezionamento

Bottomless glass bottle. Contents are inside inserted fused cone.

Pittogrammi

Health hazardExclamation mark

Avvertenze

Warning

Indicazioni di pericolo

Classi di pericolo

Carc. 2 - Skin Sens. 1

Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 2

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable

Dispositivi di protezione individuale

Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges


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Certificati d'analisi (COA)

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J T Spadaro et al.
Applied and environmental microbiology, 58(8), 2397-2401 (1992-08-01)
Under nitrogen-limiting, secondary metabolic conditions, the white rot basidiomycete Phanerochaete chrysosporium extensively mineralized the specifically 14C-ring-labeled azo dyes 4-phenylazophenol, 4-phenylazo-2-methoxyphenol, Disperse Yellow 3 [2-(4'-acetamidophenylazo)-4-methylphenol], 4-phenylazoaniline, N,N-dimethyl-4-phenylazoaniline, Disperse Orange 3 [4-(4'-nitrophenylazo)-aniline], and Solvent Yellow 14 (1-phenylazo-2-naphthol). Twelve days after addition to
J T Spadaro et al.
Archives of biochemistry and biophysics, 312(1), 301-307 (1994-07-01)
Disperse Yellow 3 [2-(4'-acetamidophenylazo)-4-methylphenol] (DY3) (I) is an important yellow dye used in industry and is also a carcinogen. Earlier we demonstrated that lignin-degrading cultures of white-rot basidiomycete Phanerochaete chrysosporium degrade DY3 to CO2. In this report, we have examined
P S Gray et al.
Cytobios, 25(99-100), 175-182 (1979-01-01)
Azo dyes have been shown to be mutagenic and toxic in a variety of organisms. The azo dye, Dispersion Yellow 3 is a pollutant in the river water supply of Northern Georgia. Preliminary and definitive studies have indicated that it
Varun Ahuja et al.
Archives of toxicology, 83(7), 691-699 (2009-02-13)
We used a modified protocol of the murine local lymph node assay (LLNA) to study the cross-sensitising potential of (a) textile dye disperse yellow 3 and its metabolite 2-amino-p-cresol, (b) two antibiotics, penicillin G and cefotiam. The test substances were
Disperse Yellow 3.
IARC monographs on the evaluation of carcinogenic risks to humans, 48, 149-159 (1990-01-01)

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