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Detail of "6925-69-5"

  • CAS Number:
  • 6925-69-5
  • Name:
  • Solvent Orange 60

  • Molecular Structure:
  • Formula:
  • C18H10N2O
  • Molecular Weight:
  • 270.29
  • Deleted CAS:
  • 59459-24-4, 61725-13-1, 61969-47-9
  • Synonyms:
  • 12-Phthaloperinone(6CI,7CI,8CI);10H-Perimidino[2,1-a]isoindol-10-one;Aminoplast Orange LFP;12H-Phthaloperin-12-one;C.I. Disperse Orange 24;C.I. Solvent Orange 60;C.I. SolventOrange 78;Diaresin Orange HS;Disperse Orange 24;KP Plast Orange 8150;KPPlast Orange HG;Macrolex Orange 3G;Oplas Orange 230;Oracet Orange G;Phthaloperinone;Sandoplast Orange 3G;Solvent Orange 78;Sumiplast Orange HRP;
  • EINECS:
  • 230-049-5
  • Density:
  • 1.404 g/cm3
  • Boiling Point:
  • 522.368 °C at 760 mmHg
  • Flash Point:
  • 269.719 °C
  • Solubility:
  • Insoluble in water

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CAS No.6925-69-5 Solvent Orange 60Competitive Product

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CAS No.6925-69-5 Solvent Orange 60

Solvent Orange 60 Identification Name Solvent Orange 60 Synonyms C.I. 564100; C.I. Solvent Orange 78; Transparent Orange 3G; 10H-Perimidino[2,1-a]isoindol-10-one; 12H-Phthaloperin-12-one Molecular Structure Molecular Formula C18H10N2O Molecular Weig

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CAS No.6925-69-5 Solvent Orange 60

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CAS No.6925-69-5 Solvent Orange 60

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CAS No.6925-69-5 Solvent Orange 60

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CAS No.6925-69-5 Solvent Orange 60

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CAS No.6925-69-5 Solvent Orange 60

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CAS No.6925-69-5 Solvent Orange 60

Assay:99%  Appearance:Yellowish or...  Package:1kg,5kg,25kg...Storage:cool,dry,pre...  Transportation:by sea,by ai...

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CAS No.6925-69-5 Solvent Orange 60

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CAS No.6925-69-5 Solvent Orange 60

For plastics, industrial oils and fats used and pre-colored spun polyester

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CAS No.6925-69-5 Solvent Orange 60

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Reference

Phthaloperinone derivatives
Phthaloperinone derivatives. Watanabe, Koichi; Harada, Hiroaki (Yamamoto Synthetic Chemical Co., Ltd., Japan). Japan. Kokai JP 51119032 19 Oct 1976 Showa, 3 pp. (Japanese). (Japan). CODEN: JKXXAF. CLASS: IC: C09B057-00. APPLICATION: JP 75-44113 10 Apr 1975. DOCUMENT TYPE: Patent CA Section: 40 (Dyes, Fluorescent Whitening Agents, and Photosensitizers) Section cross-reference(s): 28 I [R = H (II) [6925-69-5], Cl [20749-68-2], Br [26011-65-4]] were prepd. from 1,8-RC10H6NO2 (R = NH2, NO2) and phthalic anhydride deriv. in the presence of reducing agents. For example, 8-nitro-1-naphthalenamine [3229-89-8] and phthalic anhydride [85-44-9] in boiling AcOH was treated with Fe powder for 8 h, filtered, and the filter cake was washed with 5% H2SO4 at 90.In this experiment, several chemicals are used like 3229-89-8 and 117-08-8 degree. to give II. .
Phthaloperinone dyes
Phthaloperinone dyes. Watanabe, Koichi; Harada, Hiroaki (Yamamoto Synthetic Chemical Co., Ltd., Japan). Japan. Kokai JP 51138718 30 Nov 1976 Showa, 4 pp. (Japanese). (Japan). CODEN: JKXXAF. CLASS: IC: C09B057-00. APPLICATION: JP 75-48903 21 Apr 1975. DOCUMENT TYPE: Patent CA Section: 40 (Dyes, Fluorescent Whitening Agents, and Photosensitizers) Section cross-reference(s): 28 Phthaloperinones I [R = H (II) [6925-69-5], Cl [20749-68-2]] were prepd. in one step from crude nitration products of naphthalene. 602-38-0 and 20749-68-2 which are cas registry numbers of chemicals are mentioned. For example, dinitronaphthalene [60% 1,8-isomer (III) [602-38-0], 35% 1,5-isomer], phthalic anhydride [85-44-9], and Fe were stirred in AcOH at 80.degree. for 12 h, and the ppt. recrystd. from AcOH to give 74% (based on III) II as red powder, comparable in fastness, shade, and bleed resistance in polystyrene [9003-53-6] (orange shade) and ABS [9003-56-9] (red shade), to conventional product obtained from 1,8-diaminonaphthalene. .
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