词条 | Pigment Yellow 16 |
释义 |
| ImageFile = YellowPig5thTry.png | ImageSize = 320 | ImageAlt = | IUPACName = | OtherNames = |Section1={{Chembox Identifiers | CASNo = 5979-28-2 | EINECS = 227-783-3 | PubChem = 22288 | ChemSpiderID = 20921 | SMILES = Clc1cc(Cl)ccc1/N=N/C(C(=O)C)C(=O)Nc2ccc(cc2C)-c3cc(C)c(cc3)NC(=O)C(C(=O)C)/N=N/c4ccc(Cl)cc4Cl | StdInChI = 1S/C34H28Cl4N6O4/c1-17-13-21(5-9-27(17)39-33(47)31(19(3)45)43-41-29-11-7-23(35)15-25(29)37)22-6-10-28(18(2)14-22)40-34(48)32(20(4)46)44-42-30-12-8-24(36)16-26(30)38/h5-16,31-32H,1-4H3,(H,39,47)(H,40,48)/b43-41+,44-42+ | StdInChIKey = JFMYRCRXYIIGBB-CHQNLTHESA-N }} |Section2={{Chembox Properties | C=34 | H=28 | Cl=4 | N=6 | O=4 | Appearance = Yellow solid | Density = | MeltingPt = | BoilingPt = | Solubility = }} |Section3={{Chembox Hazards | MainHazards = | FlashPt = | AutoignitionPt = }} }} Pigment Yellow 16 is an organic compound that is classified as a diarylide pigment. Pigment Yellow 16 is used as a yellow colorant, and is classified as an arylide yellow. Also called permanent yellow, its color index number is 20040.[1] The compound is obtained via acetoacetylation of o-tolidine using diketene. The resulting bisacetoacetylated compound is coupled with two equiv of the diazonium salt obtained from 2,4-dichloroaniline.[2] References1. ^{{cite web |title=The Color of Art Pigment Database: Pigment Yellow, PY |url=http://www.artiscreation.com/yellow.html#.W3YMbpNKgno |website=Art is Creation}} 2. ^K. Hunger. W. Herbst "Pigments, Organic" in Ullmann's Encyclopedia of Industrial Chemistry, Wiley-VCH, Weinheim, 2012. {{DOI|10.1002/14356007.a20_371}} 5 : Biphenyls|Organic pigments|Shades of yellow|Chloroarenes|Diarylide pigments |
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