Knowledge (XXG)

SS220

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219: 33: 24: 364:. SS220 has a slightly fruity odor, tends not to provoke allergic skin reactions, lasts longer on the skin than other repellents, does not have an oily consistency, and does not tend to plasticize. Its principal disadvantage is that only one 360:
and has been found to "exert repellent and deterrent effects upon the behavior of mosquitoes and sand flies". In the field, it has been shown to provide significantly better protection than
410:"Synthesis and Repellent Efficacy of a New Chiral Piperidine Analog: Comparison with Deet and Bayrepel Activity in Human-Volunteer Laboratory Assays Against 258: 357: 579: 120: 233: 554: 477: 422: 330: 176: 197: 601: 460: 372:. As of 2007 the chemical had not been registered, as the costs involved in registration are prohibitive. 616: 606: 45: 611: 214: 86: 242:
InChI=1S/C13H21NO/c1-11-7-5-6-10-14(11)13(15)12-8-3-2-4-9-12/h2-3,11-12H,4-10H2,1H3/t11-,12+/m0/s1
546: 516:"Laboratory and Field Evaluation of SS220 and Deet Against Mosquitoes in Queensland, Australia" 461:"Repellent and Deterrent Effects of SS220, Picaridin, and Deet Suppress Human Blood Feeding by 575: 538: 496: 441: 140: 569: 530: 486: 431: 346: 281: 96: 218: 185: 324: 595: 514:
Frances, Stephen P.; Mackenzie, Donna O.; Klun, Jerome A.; Debboun, Mustapha (2009).
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of the molecule is active, meaning it will be much more costly to produce than
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Mustapha Debboun; Stephen P. Frances; Daniel Strickman (25 October 2006).
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Klun, J. A.; Khrimian, A.; Margaryan, A.; Kramer, M.; Debboun, M. (2003).
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Except where otherwise noted, data are given for materials in their
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Klun, Jerome A.; Khrimian, Ashot; Debbound, Mustapha (2006).
202: 52:-(2-methylpiperidin-1-yl)cyclohex-3-ene-1-carboxamide 523:
Journal of the American Mosquito Control Association
384:, another substituted-piperidine insect-repellent 571:Insect Repellents: Principles, Methods, and Uses 164: 95: 68:)-Methylpiperidinyl-3-cyclohexen- 1-carboxamide 354:Chemicals Affecting Insect Behavior Laboratory 8: 217: 139: 15: 490: 435: 184: 400: 358:United States Department of Agriculture 263: 238: 213: 245:Key: KRHYGGFLEBNTHQ-NWDGAFQWSA-N 7: 557:from the original on April 8, 2013. 155: 14: 352:It was developed in 2002 at the 349:with a broad range of efficacy. 299: 293: 31: 22: 390:, Experimental insect repellent 327:(at 25 °C , 100 kPa). 302: 287: 1: 478:Journal of Medical Entomology 423:Journal of Medical Entomology 633: 437:10.1603/0022-2585-40.3.293 321: 274: 254: 229: 79: 57: 44: 39: 30: 21: 574:. CRC. pp. 10–11. 492:10.1093/jmedent/43.1.34 74:)-1--2-methylpiperidine 266:C1CCCCN1C(=O)2CCC=CC2 471:Phlebotomus papatasi 467:Anopheles stephensi 416:Anopheles stephensi 317: g·mol 18: 331:Infobox references 16: 602:Insect repellents 581:978-1-4200-0665-0 535:10.2987/08-5823.1 339:Chemical compound 337: 336: 198:CompTox Dashboard 121:Interactive image 624: 586: 585: 565: 559: 558: 520: 511: 505: 504: 494: 456: 450: 449: 439: 405: 347:insect repellent 316: 304: 301: 295: 289: 282:Chemical formula 222: 221: 206: 204: 188: 168: 157: 143: 123: 99: 35: 26: 19: 632: 631: 627: 626: 625: 623: 622: 621: 592: 591: 590: 589: 582: 567: 566: 562: 518: 513: 512: 508: 458: 457: 453: 407: 406: 402: 397: 378: 340: 333: 328: 314: 298: 292: 284: 270: 267: 262: 261: 250: 247: 246: 243: 237: 236: 225: 215:DTXSID101186531 207: 200: 191: 171: 158: 146: 126: 113: 102: 89: 75: 69: 53: 12: 11: 5: 630: 628: 620: 619: 614: 609: 604: 594: 593: 588: 587: 580: 560: 529:(2): 174–178. 506: 451: 430:(3): 293–299. 399: 398: 396: 393: 392: 391: 385: 377: 374: 338: 335: 334: 329: 325:standard state 322: 319: 318: 312: 306: 305: 296: 290: 285: 280: 277: 276: 272: 271: 269: 268: 265: 257: 256: 255: 252: 251: 249: 248: 244: 241: 240: 232: 231: 230: 227: 226: 224: 223: 210: 208: 196: 193: 192: 190: 189: 181: 179: 173: 172: 170: 169: 161: 159: 151: 148: 147: 145: 144: 136: 134: 128: 127: 125: 124: 116: 114: 107: 104: 103: 101: 100: 92: 90: 85: 82: 81: 77: 76: 59: 55: 54: 48: 42: 41: 37: 36: 28: 27: 13: 10: 9: 6: 4: 3: 2: 629: 618: 615: 613: 610: 608: 605: 603: 600: 599: 597: 583: 577: 573: 572: 564: 561: 556: 552: 548: 544: 540: 536: 532: 528: 524: 517: 510: 507: 502: 498: 493: 488: 484: 480: 479: 474: 472: 468: 464: 463:Aedes aegypti 455: 452: 447: 443: 438: 433: 429: 425: 424: 419: 417: 413: 412:Aedes aegypti 404: 401: 394: 389: 386: 383: 380: 379: 375: 373: 371: 367: 363: 359: 355: 350: 348: 344: 332: 326: 320: 313: 311: 308: 307: 286: 283: 279: 278: 273: 264: 260: 253: 239: 235: 228: 220: 216: 212: 211: 209: 199: 195: 194: 187: 183: 182: 180: 178: 175: 174: 167: 163: 162: 160: 154: 150: 149: 142: 138: 137: 135: 133: 130: 129: 122: 118: 117: 115: 111: 106: 105: 98: 94: 93: 91: 88: 84: 83: 78: 73: 67: 63: 56: 51: 47: 43: 38: 34: 29: 25: 20: 617:Cyclohexenes 607:Carboxamides 570: 563: 526: 522: 509: 485:(1): 34–39. 482: 476: 470: 466: 462: 454: 427: 421: 415: 411: 403: 366:stereoisomer 353: 351: 342: 341: 80:Identifiers 71: 65: 61: 58:Other names 49: 612:Piperidines 275:Properties 97:298207-27-9 596:Categories 395:References 310:Molar mass 186:A8MXE67MXB 132:ChemSpider 108:3D model ( 87:CAS Number 46:IUPAC name 555:Archived 551:27171560 543:19653499 501:16506445 446:12943107 382:Icaridin 376:See also 370:icaridin 166:40579125 141:32787838 356:of the 315:207.317 153:PubChem 578:  549:  541:  499:  469:, and 444:  345:is an 259:SMILES 40:Names 17:SS220 547:S2CID 519:(PDF) 388:VUAA1 343:SS220 234:InChI 110:JSmol 576:ISBN 539:PMID 497:PMID 442:PMID 414:and 362:DEET 177:UNII 531:doi 487:doi 432:doi 203:EPA 156:CID 64:,2' 598:: 553:. 545:. 537:. 527:25 525:. 521:. 495:. 483:43 481:. 475:. 465:, 440:. 428:40 426:. 420:. 297:21 291:13 70:(2 60:(1 584:. 533:: 503:. 489:: 473:" 448:. 434:: 418:" 303:O 300:N 294:H 288:C 205:) 201:( 112:) 72:S 66:S 62:S 50:N

Index



IUPAC name
CAS Number
298207-27-9
JSmol
Interactive image
ChemSpider
32787838
PubChem
40579125
UNII
A8MXE67MXB
CompTox Dashboard
DTXSID101186531
Edit this at Wikidata
InChI
SMILES
Chemical formula
Molar mass
standard state
Infobox references
insect repellent
United States Department of Agriculture
DEET
stereoisomer
icaridin
Icaridin
VUAA1
"Synthesis and Repellent Efficacy of a New Chiral Piperidine Analog: Comparison with Deet and Bayrepel Activity in Human-Volunteer Laboratory Assays Against Aedes aegypti and Anopheles stephensi"

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