Knowledge (XXG)

1-Naphthylamine

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300: 205: 44: 35: 569: 792: 582: 735:. It forms small needles, very sparingly soluble in water. Upon treatment with the bis(diazonium) derivative of benzidine, 1-aminonaphthalene-4-sulfonic acid gives 349: 865: 826: 551: 314: 519: 709: 870: 842: 589: 257: 43: 278: 860: 475: 200: 690: 620: 162: 34: 56: 681:
reduces the unsubstituted ring, giving tetrahydro-1-naphthylamine. This tetrahydro compound yields
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It is listed as one of the 13 carcinogens covered by the OSHA General Industry Standards.
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readily, and turns brown on exposure to air. It is the precursor to a variety of dyes.
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in colorless needles which melt at 50 °C. It possesses a disagreeable odor,
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Except where otherwise noted, data are given for materials in their
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47 to 50 °C (117 to 122 °F; 320 to 323 K)
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InChI=1S/C10H9N/c11-10-7-3-5-8-4-1-2-6-9(8)10/h1-7H,11H2
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InChI=1/C10H9N/c11-10-7-3-5-8-4-1-2-6-9(8)10/h1-7H,11H2
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National Institute for Occupational Safety and Health
731:to 170–180 °C in the presence of crystallized 809:Gerald Booth (2005). "Naphthalene Derivatives". 245: 97: 811:Ullmann's Encyclopedia of Industrial Chemistry 8: 710:sulfonic acid derivatives of 1-naphthylamine 696:At 200 °C in sulfuric acid, it converts to 404:Colorless crystals (reddish-purple in air) 298: 203: 181: 26: 804: 802: 265: 787:NIOSH Pocket Guide to Chemical Hazards. 770: 354: 319: 294: 782: 780: 778: 776: 774: 447:301 °C (574 °F; 574 K) 194: 506:157 °C; 315 °F; 430 K 326:Key: RUFPHBVGCFYCNW-UHFFFAOYSA-N 161: 141: 7: 336:Key: RUFPHBVGCFYCNW-UHFFFAOYAD 236: 220: 25: 552:1,8-Bis(dimethylamino)naphthalene 712:are used for the preparation of 567: 42: 33: 563:(at 25 °C , 100 kPa). 1: 723:An important derivative is 488:-127.6·10 cm/mol (HCl salt) 887: 396:143.19 g/mol 627:Preparation and reactions 557: 524: 495: 365: 345: 310: 81: 67: 55: 50: 41: 32: 866:IARC Group 3 carcinogens 819:10.1002/14356007.a17_009 635:1-nitronaphthalene with 843:OSHA Standard 1910.1003 813:. Weinheim: Wiley-VCH. 756:Used in preparation of 476:Magnetic susceptibility 691:potassium permanganate 661:with solutions of its 631:It can be prepared by 70:(Naphthalen-1-yl)amine 871:1-Naphthyl compounds 57:Preferred IUPAC name 454:Solubility in water 29: 645:steam distillation 590:Infobox references 525:Related compounds 76:1-Aminonaphthalene 61:Naphthalen-1-amine 27: 669:converts it into 641:hydrochloric acid 598:Chemical compound 596: 595: 531:Related compounds 512:Safety data sheet 279:CompTox Dashboard 123:Interactive image 16:(Redirected from 878: 845: 840: 834: 832: 806: 797: 796: 784: 725:naphthionic acid 671:1-naphthoquinone 651:Oxidizing agents 580: 574: 571: 570: 373:Chemical formula 303: 302: 287: 285: 269: 249: 238: 224: 207: 196: 185: 165: 145: 125: 101: 46: 37: 30: 28:1-Naphthylamine 21: 886: 885: 881: 880: 879: 877: 876: 875: 851: 850: 849: 848: 841: 837: 829: 808: 807: 800: 786: 785: 772: 767: 753: 745: 706: 655:ferric chloride 629: 602:1-Naphthylamine 599: 592: 587: 586: 585:  ?) 576: 572: 568: 564: 550: 546: 542: 538: 536:2-Naphthylamine 532: 491: 485:-98.8·10 cm/mol 479: 469:1 mmHg (104°C) 456: 385: 381: 375: 361: 358: 357:Nc1c2ccccc2ccc1 353: 352: 341: 338: 337: 334: 328: 327: 324: 318: 317: 306: 288: 281: 272: 252: 239: 227: 188: 168: 148: 128: 115: 104: 91: 77: 75: 74:α-Naphthylamine 73: 72:1-Naphthylamine 71: 63: 62: 23: 22: 18:1-naphthylamine 15: 12: 11: 5: 884: 882: 874: 873: 868: 863: 861:Naphthylamines 853: 852: 847: 846: 835: 827: 798: 769: 768: 766: 763: 762: 761: 752: 749: 744: 741: 705: 702: 657:, give a blue 628: 625: 597: 594: 593: 588: 566: 565: 561:standard state 558: 555: 554: 533: 530: 527: 526: 522: 521: 515: 508: 507: 504: 498: 497: 493: 492: 490: 489: 486: 482: 480: 474: 471: 470: 467: 465:Vapor pressure 461: 460: 459:0.002% (20°C) 457: 452: 449: 448: 445: 439: 438: 435: 429: 428: 425: 419: 418: 412: 406: 405: 402: 398: 397: 394: 388: 387: 383: 379: 376: 371: 368: 367: 363: 362: 360: 359: 356: 348: 347: 346: 343: 342: 340: 339: 335: 332: 331: 329: 325: 322: 321: 313: 312: 311: 308: 307: 305: 304: 291: 289: 277: 274: 273: 271: 270: 262: 260: 254: 253: 251: 250: 242: 240: 232: 229: 228: 226: 225: 217: 215: 209: 208: 198: 190: 189: 187: 186: 178: 176: 170: 169: 167: 166: 158: 156: 150: 149: 147: 146: 138: 136: 130: 129: 127: 126: 118: 116: 109: 106: 105: 103: 102: 94: 92: 87: 84: 83: 79: 78: 69: 65: 64: 60: 59: 53: 52: 48: 47: 39: 38: 24: 14: 13: 10: 9: 6: 4: 3: 2: 883: 872: 869: 867: 864: 862: 859: 858: 856: 844: 839: 836: 830: 828:9783527303854 824: 820: 816: 812: 805: 803: 799: 794: 790: 783: 781: 779: 777: 775: 771: 764: 759: 755: 754: 750: 748: 742: 740: 738: 734: 730: 729:sulfuric acid 726: 721: 719: 715: 711: 703: 701: 699: 694: 692: 688: 684: 680: 676: 672: 668: 664: 660: 656: 652: 648: 646: 642: 638: 634: 626: 624: 622: 618: 614: 611:derived from 610: 607: 603: 591: 584: 579: 562: 556: 553: 549: 545: 541: 537: 534: 529: 528: 523: 520: 518: 516: 513: 510: 509: 505: 503: 500: 499: 494: 487: 484: 483: 481: 477: 473: 472: 468: 466: 463: 462: 458: 455: 451: 450: 446: 444: 443:Boiling point 441: 440: 436: 434: 433:Melting point 431: 430: 426: 424: 421: 420: 416: 413: 411: 408: 407: 403: 400: 399: 395: 393: 390: 389: 377: 374: 370: 369: 364: 355: 351: 344: 330: 320: 316: 309: 301: 297: 296:DTXSID7020920 293: 292: 290: 280: 276: 275: 268: 264: 263: 261: 259: 256: 255: 248: 244: 243: 241: 235: 231: 230: 223: 219: 218: 216: 214: 211: 210: 206: 202: 199: 197: 195:ECHA InfoCard 192: 191: 184: 180: 179: 177: 175: 172: 171: 164: 160: 159: 157: 155: 152: 151: 144: 140: 139: 137: 135: 132: 131: 124: 120: 119: 117: 113: 108: 107: 100: 96: 95: 93: 90: 86: 85: 80: 66: 58: 54: 49: 45: 40: 36: 31: 19: 838: 810: 746: 722: 707: 695: 679:amyl alcohol 667:Chromic acid 649: 643:followed by 630: 617:crystallizes 601: 600: 82:Identifiers 68:Other names 733:oxalic acid 704:Use in dyes 683:adipic acid 677:in boiling 659:precipitate 613:naphthalene 544:Naphthalene 502:Flash point 427:1.114 g/cm 401:Appearance 366:Properties 201:100.004.672 163:ChEMBL57394 143:CHEBI:50450 855:Categories 765:References 698:1-naphthol 653:, such as 540:1-Naphthol 392:Molar mass 267:9753I242R5 174:ChemSpider 110:3D model ( 89:CAS Number 758:aptiganel 737:Congo red 795:(NIOSH). 751:See also 687:oxidized 633:reducing 621:sublimes 606:aromatic 496:Hazards 478:(χ) 386:N 99:134-32-7 789:"#0441" 714:azo dye 583:what is 581: ( 548:Aniline 423:Density 415:ammonia 234:PubChem 825:  743:Safety 718:cotton 675:Sodium 604:is an 578:verify 575:  514:(SDS) 417:-like 350:SMILES 222:C14790 154:ChEMBL 51:Names 685:when 663:salts 609:amine 315:InChI 134:ChEBI 112:JSmol 823:ISBN 708:The 639:and 637:iron 410:Odor 258:UNII 247:8640 213:KEGG 183:8319 815:doi 720:. 693:. 689:by 647:. 284:EPA 237:CID 857:: 821:. 801:^ 791:. 773:^ 739:. 700:. 673:. 665:. 380:10 833:. 831:. 817:: 760:. 573:Y 384:9 382:H 378:C 286:) 282:( 114:) 20:)

Index

1-naphthylamine
Skeletal formula
Ball-and-stick model
Preferred IUPAC name
CAS Number
134-32-7
JSmol
Interactive image
ChEBI
CHEBI:50450
ChEMBL
ChEMBL57394
ChemSpider
8319
ECHA InfoCard
100.004.672
Edit this at Wikidata
KEGG
C14790
PubChem
8640
UNII
9753I242R5
CompTox Dashboard
DTXSID7020920
Edit this at Wikidata
InChI
SMILES
Chemical formula
Molar mass

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