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Merck
모든 사진(2)

문서

09215

Supelco

Pigment Orange 5

analytical standard

동의어(들):

1-[(2,4-Dinitrophenyl)azo]-2-naphthol, Permanent red 2G

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About This Item

실험식(Hill 표기법):
C16H10N4O5
CAS Number:
Molecular Weight:
338.27
색상 지수 번호:
12075
Beilstein:
964718
EC Number:
MDL number:
UNSPSC 코드:
85151701
PubChem Substance ID:
NACRES:
NA.24

Grade

analytical standard

Quality Level

분석

≥98.0% (HPLC)

유통기한

limited shelf life, expiry date on the label

기술

HPLC: suitable
gas chromatography (GC): suitable

mp

310-320 °C

응용 분야

cleaning products
cosmetics
food and beverages
personal care

형식

neat

SMILES string

Oc1ccc2ccccc2c1\N=N\c3ccc(cc3[N+]([O-])=O)[N+]([O-])=O

InChI

1S/C16H10N4O5/c21-15-8-5-10-3-1-2-4-12(10)16(15)18-17-13-7-6-11(19(22)23)9-14(13)20(24)25/h1-9,21H/b18-17+

InChI key

HBHZKFOUIUMKHV-ISLYRVAYSA-N

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일반 설명

Pigment orange 5 is an azo pigment, which can be produced industrially by a diazotization and coupling sequence in which diazotized dinitroaniline is coupled into β-naphthol.

포장

Bottomless glass bottle. Contents are inside inserted fused cone.

픽토그램

Health hazard

신호어

Warning

유해 및 위험 성명서

예방조치 성명서

Hazard Classifications

Carc. 2 - Muta. 2

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point (°F)

Not applicable

Flash Point (°C)

Not applicable


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문서 라이브러리 방문

Coatings Materials and Surface Coatings (2006)
P Møller et al.
Teratogenesis, carcinogenesis, and mutagenesis, 18(1), 9-16 (1998-05-20)
The induction of DNA damage by commonly used printing ink pigments, C.I. pigment orange 5 (C.I. 12075) and C.I. pigment yellow 12 (C.I. 21090), was investigated in freshly isolated rat hepatocytes with the comet assay. C.I. pigment yellow 12 is
Pigment Orange 5: crystal structure determination from a non-indexed X-ray powder diagram.
Schmidt U M, et al.
Zeitschrift fur Kristallographie, 222(1), 30-33 (2007)
A L Scher
Journal - Association of Official Analytical Chemists, 68(3), 474-477 (1985-05-01)
A method is described for the determination of the intermediates in D&C Orange No. 17 by reverse phase liquid chromatography. The pigment is dissolved in boiling dioxane and then precipitated. The filtrate is chromatographed by isocratic elution, which is followed

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