Chemistry:Para red

From HandWiki
Para red
Para Red Formula V.1.svg
Names
Preferred IUPAC name
1-[(E)-(4-Nitrophenyl)diazenyl]naphthalen-2-ol
Other names
1-[(4-Nitrophenyl)azo]-2-naphthalenol, 1-((4-nitrophenyl)azo)-2-naphthol, 1-[(p-nitrophenyl)azo]-2-naphthalenol, 1-[(p-nitrophenyl)azo]-2-naphthol, 1-[(E)-(4-Nitrophenyl)diazenyl]-2-naphthol, paranitraniline red, Pigment Red 1, C.I. 12070, Recolite Para Red B, Carnelio Para Red BS
Identifiers
3D model (JSmol)
ChEMBL
ChemSpider
EC Number
  • 229-093-8
UNII
Properties
C16H11N3O3
Molar mass 293.282 g·mol−1
Appearance Red solid
Melting point 248 to 252 °C (478 to 486 °F; 521 to 525 K)
Hazards
GHS pictograms GHS07: Harmful
GHS Signal word Warning
H315, H319, H335
P261, P264, P271, P280, P302+352, P304+340, P305+351+338, P312, P321, P332+313, P337+313, P362, P403+233, P405, P501
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
☒N verify (what is ☑Y☒N ?)
Infobox references
Tracking categories (test):

Para red (paranitraniline red, Pigment Red 1, C.I. 12070) is a dye. Chemically, it is similar to Sudan I. It was discovered in 1880 by von Gallois and Ullrich and was the first azo dye. It dyes cellulose fabrics a brilliant red color, but is not very fast. The dye can be washed away easily from cellulose fabrics if not dyed correctly. Acidic and basic stages both occur during the standard formation of Para Red, and acidic or basic byproducts may be present in the final product.

Synthesis

Para red is prepared by diazotization of para-nitroaniline at ice-cold temperatures, followed by coupling with β-naphthol:[1]

Synthesis of Para Red

Regulation

Para red is not approved for use in food in any jurisdiction. In 2005, Old El Paso dinner kits were found to be contaminated with the dye and removed from supermarket shelves.[2][3]

References

External links