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Detail of "1658-56-6"

  • CAS Number:
  • 1658-56-6
  • Name:

  • 1-Naphthalenesulfonicacid, 4-[2-(2-hydroxy-1-naphthalenyl)diazenyl]-, sodium salt (1:1)

  • Superlist Name:
  • Acid Red 88
  • Molecular Structure:
  • Formula:
  • C20H14N2O4S.Na
  • Molecular Weight:
  • 401.38
  • Deleted CAS:
  • 163442-07-7|39309-87-0
  • Synonyms:
  • Naphthalene Red J (6CI);2-Naphthol RedJ;Acid Leather Red ROC;Acid Red 88;AcidRed A;Acid Red AV;Acid Red G;Acid Rose AV;Amacid Fast Red A;Anadurm RedA-ROC;Apollo Acid Rocceline;Azo Acid RedGS;Benzyl Red ROC;Benzyl Red S;Bucacid FastRed A;C.I. 15620;Cavalene Red A;Colacid Red AV;Conacid Red MM;Dai-ei Roccelline;Derma Fur Red R 150;Dinacid Fast Red A;Dycosacid Red A;Eriosin Roccelline;Ext D and C Red No. 8;Fabracid Red S-A;FastRed A;Fast Red A (acid dye);Fast Red AG;Fast RedAV;Fast Red MA;Fast Red S;Fur Red KB;Hispacid Fast Red A;Indacid Acid Red A;JapanRed No. 506;Kayaku Roccelline;Kemacid Fast Red A;LurazolRed E;Multacid Red A;Multicuer Red A;Naphthalene Red JS;Neklacid Fast Red A;New Red WO;Peony;Pontacyl Fast Red AS;Red No. 506;Rifa Acid Roccelline NS;Rocceline;Roccelline A;Roccelline KG;Roccelline NS;Roccelline S;Romexal Red AV;Shikiso Roccelline;
  • EINECS:
  • 216-760-3
  • Melting Point:
  • 280 °C
  • Solubility:
  • soluble in water, ethanol, ethylene glycol ether, slightly soluble in acetone, soluble in concentrated acid and dilute sodium hydroxide solution
  • Appearance:
  • Dark red to maroon powder
  • Safety:
  • 24/25 Details
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CAS No.1658-56-6 Acid Red 88Competitive Product

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Reference

The effect of some sulfonated Novolacs and related compounds on the adsorption of acid dyes by nylon 6
The effect of some sulfonated Novolacs and related compounds on the adsorption of acid dyes by nylon 6. Cook, Christopher C.Some chemicals with cas registry numbers like 1658-56-6 are also used.; Herbert, Colin G. (Sch. Colour Chem. Colour Technol., Univ. Bradford, Bradford, Engl.). J. Appl. Chem.There are some reagents like 1658-56-6 is used in this study. Biotechnol., 28(2), 105-15 (English) 1978. CODEN: JACBBD. ISSN: 0375-9210. DOCUMENT TYPE: Journal CA Section: 39 (Textiles) The absorption restraining effects on 5 dyes, e.g. C.I. Acid Red 88 [1658-56-6], of treatment of nylon 6 with 7 formaldehyde-phenol copolymer [9003-35-4] samples (mol. wt. 500-850) their sulfonated derivs., and 5 unsulfonated and 1 sulfonated Novolak model compd. were examd. Sulfonation of the resins gave increased restraining effects towards the dyes; these effects were attributed to a redn. in the no. of pos. charged sites on the nylon mols. The sulfonate restraining effects did not increase steadily with increasing mol. wt. and the most efficient syntan contained 5-10 condensed sulfonated PhOH mols. Comparable restraining effects were obsd. for 2,2'-dihydroxy-1,1'-dinaphthylmethane [1096-84-0] applied to nylon as a dispersion. ..
Self-quenching interaction between ferrocene units in photooxidation-reduction sensitized by copolymers of 1-ferrocenylethyl methacrylate
Self-quenching interaction between ferrocene units in photooxidation-reduction sensitized by copolymers of 1-ferrocenylethyl methacrylate. Nakahira, Takayuki; Minami, Chiyo; Iwabuchi, Susumu; Kojima, Kuniharu (Fac. Eng., Chiba Univ., Chiba, Japan). Makromol. Chem., 179(6), 1593-600 (English) 1978. CODEN: MACEAK. ISSN: 0025-116X. DOCUMENT TYPE: Journal CA Section: 35 (Synthetic High Polymers) 1-Ferrocenylethyl methacrylate-styrene copolymer [67228-49-3] and 1-ferrocenylethyl methacrylate-Me methacrylate copolymer [67228-50-6] were prepd. and their photosensitization of the redox reaction between L-ascorbic acid [50-81-7] and Fast Red A [1658-56-6] were studied in DMF. With both copolymers the higher the 1-ferrocenylethyl methacrylate (I) content, the lower the relative quantum yield of the sensitization. The obsd. decrease in the relative quantum yield was interpreted in terms of Perrin's model of static quenching interaction between excited and near-by ground-state ferrocene units. The mean sequence length of I in the polymer was an appropriate parameter for the local ferrocene concn. with respect to the polymer. Both energy migration and quenching interaction were thought to occur among nearest-neighbor ferrocene units along the polymer chain, with quenching interaction prevailing over energy migration.
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