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{{Chembox | {{Chembox | ||
| ImageFile = | | ImageFile = PigYell74Taut.svg | ||
| ImageSize = | | ImageSize = 120 | ||
| ImageAlt = | | ImageAlt = | ||
| IUPACName = | | IUPACName = | ||
| OtherNames = | | OtherNames = Hansa Yellow 5GXB | ||
|Section1={{Chembox Identifiers | |Section1={{Chembox Identifiers | ||
| CASNo = 6358-31-2 | | CASNo = 6358-31-2 | ||
| CASNo_Comment = | | CASNo_Comment = | ||
| ChemSpiderID = 21172327 | |||
| CASNo1 = | |||
| |
| PubChem = 22829 | ||
| |
| UNII = 85338B499O | ||
| |
| EINECS = 228-768-4 | ||
| SMILES = N(=NC(C(NC1=C(OC)C=CC=C1)=O)C(C)=O)C2=C(OC)C=C(N(=O)=O)C=C2 | |||
| InChI = 1S/C18H18N4O6/c1-11(23)17(18(24)19-13-6-4-5-7-15(13)27-2)21-20-14-9-8-12(22(25)26)10-16(14)28-3/h4-10,17H,1-3H3,(H,19,24) | |||
| InChIKey = ZTISORAUJJGACZ-UHFFFAOYSA-N | |||
}} | |||
|Section2={{Chembox Properties | |Section2={{Chembox Properties | ||
| C=18|H=18|N=4|O=6 | | C=18|H=18|N=4|O=6 | ||
| MolarMass = | |||
| Appearance = yellow powder | | Appearance = yellow powder | ||
| Density = 1.436 g/cm<sup>3</sup> | | Density = 1.436 g/cm<sup>3</sup> | ||
| |
| MeltingPtC = 290 | ||
| MeltingPt_notes = | | MeltingPt_notes = Decomposes | ||
| BoilingPt = | | BoilingPt = | ||
| BoilingPt_notes = | | BoilingPt_notes = | ||
| Solubility = }} | | Solubility = 7.6 µg/L}} | ||
|Section3={{Chembox Hazards | |Section3={{Chembox Hazards | ||
| MainHazards = | | MainHazards = | ||
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| AutoignitionPt = }} | | AutoignitionPt = }} | ||
}} | }} | ||
'''Pigment Yellow 74''' is an ] and classified as an ]. It is an intensely yellow-green solid.<ref name=Ullmann1>{{cite encyclopedia|author=K. Hunger |author2=W. Herbst |title=Pigments, Organic|encyclopedia=Ullmann's Encyclopedia of Industrial Chemistry|publisher=Wiley-VCH|place=Weinheim|year=2012|doi=10.1002/14356007.a20_371|isbn=978-3-527-30673-2}}</ref> It is prepared by azo coupling of the diazonium derivative of ] with 2-methoxy].<ref>{{cite journal |doi=10.1016/0143-7208(91)85013-x |title=Some monoazoacetoacetanilide pigments derived from heterocyclic diazo components |date=1991 |last1=Christie |first1=Robert M. |last2=Dryburgh |first2=William T. |last3=Standring |first3=Paul N. |journal=Dyes and Pigments |volume=16 |issue=3 |pages=231–240 }}</ref> It is a flat molecule, enforced by the hydrogen-bonding via the ketohydrazide group.<ref>{{cite journal |doi=10.1107/S0108270187088723 |title=CI Pigment Yellow 74, α-(2-methoxy-4-nitrophenylhydrazono)-α-aceto-2'-methoxyacetanilide |date=1987 |last1=Whitaker |first1=A. |last2=Walker |first2=N. P. C. |journal=Acta Crystallographica Section C Crystal Structure Communications |volume=43 |issue=11 |pages=2137–2141 }}</ref> | |||
'''Pigment Yellow 74''' is an ] with intense yellow-green coloration. | |||
It is popular in ]s. It is prepared by azo coupling of the diazonium derivative of 4-nitro-2-methoxyaniline with ].<ref>{{cite journal |doi=10.1016/0143-7208(91)85013-x |title=Some monoazoacetoacetanilide pigments derived from heterocyclic diazo components |date=1991 |last1=Christie |first1=Robert M. |last2=Dryburgh |first2=William T. |last3=Standring |first3=Paul N. |journal=Dyes and Pigments |volume=16 |issue=3 |pages=231–240 }}</ref> | |||
Pigment Yellow 74 is a popular component of artist's paints<ref>{{cite journal |doi=10.1016/j.saa.2008.11.029 |title=Synthetic organic pigments of the 20th and 21st century relevant to artist's paints: Raman spectra reference collection |date=2009 |last1=Scherrer |first1=Nadim C. |last2=Stefan |first2=Zumbuehl |last3=Francoise |first3=Delavy |last4=Annette |first4=Fritsch |last5=Renate |first5=Kuehnen |journal=Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy |volume=73 |issue=3 |pages=505–524 |pmid=19136293 |bibcode=2009AcSpA..73..505S }}</ref> and ]s.<ref>{{cite journal |doi=10.1562/2004-04-06-ra-136.1 |title=Photodecomposition of Pigment Yellow 74, a Pigment Used in Tattoo Inks |date=2004 |last1=Cui |first1=Yanyan |last2=Spann |first2=Andrew P. |last3=Couch |first3=Letha H. |last4=Gopee |first4=Neera V. |last5=Evans |first5=Frederick E. |last6=Churchwell |first6=Mona I. |last7=Williams |first7=Lee D. |last8=Doerge |first8=Daniel R. |last9=Howard |first9=Paul C. |journal=Photochemistry and Photobiology |volume=80 |issue=2 |pages=175–184 |pmid=15362942 }}</ref> | Pigment Yellow 74 is a popular component of artist's paints<ref>{{cite journal |doi=10.1016/j.saa.2008.11.029 |title=Synthetic organic pigments of the 20th and 21st century relevant to artist's paints: Raman spectra reference collection |date=2009 |last1=Scherrer |first1=Nadim C. |last2=Stefan |first2=Zumbuehl |last3=Francoise |first3=Delavy |last4=Annette |first4=Fritsch |last5=Renate |first5=Kuehnen |journal=Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy |volume=73 |issue=3 |pages=505–524 |pmid=19136293 |bibcode=2009AcSpA..73..505S }}</ref> and ]s.<ref>{{cite journal |doi=10.1562/2004-04-06-ra-136.1 |title=Photodecomposition of Pigment Yellow 74, a Pigment Used in Tattoo Inks |date=2004 |last1=Cui |first1=Yanyan |last2=Spann |first2=Andrew P. |last3=Couch |first3=Letha H. |last4=Gopee |first4=Neera V. |last5=Evans |first5=Frederick E. |last6=Churchwell |first6=Mona I. |last7=Williams |first7=Lee D. |last8=Doerge |first8=Daniel R. |last9=Howard |first9=Paul C. |journal=Photochemistry and Photobiology |volume=80 |issue=2 |pages=175–184 |pmid=15362942 }}</ref> | ||
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<references /> | <references /> | ||
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] | |||
] | ] | ||
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Latest revision as of 02:45, 9 January 2025
Names | |
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Other names Hansa Yellow 5GXB | |
Identifiers | |
CAS Number | |
3D model (JSmol) | |
ChemSpider | |
ECHA InfoCard | 100.026.153 |
EC Number |
|
PubChem CID | |
UNII | |
CompTox Dashboard (EPA) | |
InChI
| |
SMILES
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Properties | |
Chemical formula | C18H18N4O6 |
Molar mass | 386.364 g·mol |
Appearance | yellow powder |
Density | 1.436 g/cm |
Melting point | 290 °C (554 °F; 563 K) Decomposes |
Solubility in water | 7.6 µg/L |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 100 kPa). Infobox references |
Pigment Yellow 74 is an azo dye and classified as an arylide yellow. It is an intensely yellow-green solid. It is prepared by azo coupling of the diazonium derivative of 2-methoxy-4-nitroaniline with 2-methoxyacetoacetanilide. It is a flat molecule, enforced by the hydrogen-bonding via the ketohydrazide group.
Pigment Yellow 74 is a popular component of artist's paints and tattoo inks.
References
- K. Hunger; W. Herbst (2012). "Pigments, Organic". Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH. doi:10.1002/14356007.a20_371. ISBN 978-3-527-30673-2.
- Christie, Robert M.; Dryburgh, William T.; Standring, Paul N. (1991). "Some monoazoacetoacetanilide pigments derived from heterocyclic diazo components". Dyes and Pigments. 16 (3): 231–240. doi:10.1016/0143-7208(91)85013-x.
- Whitaker, A.; Walker, N. P. C. (1987). "CI Pigment Yellow 74, α-(2-methoxy-4-nitrophenylhydrazono)-α-aceto-2'-methoxyacetanilide". Acta Crystallographica Section C Crystal Structure Communications. 43 (11): 2137–2141. doi:10.1107/S0108270187088723.
- Scherrer, Nadim C.; Stefan, Zumbuehl; Francoise, Delavy; Annette, Fritsch; Renate, Kuehnen (2009). "Synthetic organic pigments of the 20th and 21st century relevant to artist's paints: Raman spectra reference collection". Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy. 73 (3): 505–524. Bibcode:2009AcSpA..73..505S. doi:10.1016/j.saa.2008.11.029. PMID 19136293.
- Cui, Yanyan; Spann, Andrew P.; Couch, Letha H.; Gopee, Neera V.; Evans, Frederick E.; Churchwell, Mona I.; Williams, Lee D.; Doerge, Daniel R.; Howard, Paul C. (2004). "Photodecomposition of Pigment Yellow 74, a Pigment Used in Tattoo Inks". Photochemistry and Photobiology. 80 (2): 175–184. doi:10.1562/2004-04-06-ra-136.1. PMID 15362942.