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BTMPS

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24: 662:
Sótonyi, P; Merkely, B; Hubay, M; Járay, J; Zima, E; Soós, P; Kovács, A; Szentmáriay, I (February 2004). "Comparative study on cardiotoxic effect of Tinuvin 770: a light stabilizer of medical plastics in rat model".
499:
Papke, RL; Craig, AG; Heinemann, SF (February 1994). "Inhibition of nicotinic acetylcholine receptors by bis (2,2,6,6-tetramethyl- 4-piperidinyl) sebacate (Tinuvin 770), an additive to medical plastics".
471: 84: 578:
Sótonyi, P; Keller, E; Járay, J; Nemes, B; Benkõ, T; Kovács, A; Tolokán, A; Rajs, I (15 July 2001). "A light stabilizer Tinuvin 770-induced toxic injury of adult rat cardiac myocytes".
220: 204:
InChI=1S/C28H52N2O4/c1-25(2)17-21(18-26(3,4)29-25)33-23(31)15-13-11-9-10-12-14-16-24(32)34-22-19-27(5,6)30-28(7,8)20-22/h21-22,29-30H,9-20H2,1-8H3
527:
Glossmann, H; Hering, S; Savchenko, A; Berger, W; Friedrich, K; Garcia, ML; Goetz, MA; Liesch, JM; Zink, DL; Kaczorowski, GJ (15 October 1993).
462: 195: 392: 338: 442: 424: 380: 529:"A light stabilizer (Tinuvin 770) that elutes from polypropylene plastic tubes is a potent L-type Ca(2+)-channel blocker" 318: 172: 704: 115: 133: 613:
Krepuska, M; Hubay, M; Zima, E; Kovacs, A; Kekesi, V; Kalasz, H; Szilagyi, B; Merkely, B; Sotonyi, P (2018).
400: 396: 139: 709: 50: 680: 644: 595: 560: 509: 672: 634: 626: 587: 550: 540: 461: 243: 104: 181: 60: 714: 639: 614: 312: 591: 698: 555: 528: 399:. It is also able to induce dose-dependent hemodynamic alterations. Similar to early 300: 485: 463:"An industrial chemical is showing up in fentanyl in the U.S., troubling scientists" 376: 161: 630: 533:
Proceedings of the National Academy of Sciences of the United States of America
665:
Toxicological Sciences : An Official Journal of the Society of Toxicology
404: 277: 95: 676: 545: 684: 648: 599: 564: 513: 615:"Hemodynamic Effects of the Light Stabilizer Tinuvin 770 in Dogs In Vivo" 364: 290: 148: 116: 311:
Except where otherwise noted, data are given for materials in their
83: 73: 23: 228:
CC1(C)CC(CC(C)(C)N1)OC(=O)CCCCCCCCC(=O)OC2CC(C)(C)NC(C)(C)C2
486:"Preparation method of hindered amine light stabilizer 770" 363:
In 2024 it was detected as an adulterant in illicitly sold
502:
The Journal of Pharmacology and Experimental Therapeutics
305:
81 to 85 °C (178 to 185 °F; 354 to 358 K)
447:
The Center for Forensic Science Research & Education
160: 425:"Bis(2,2,6,6-tetramethyl-4-piperidyl) sebacate" 59: 38:Bis(2,2,6,6-tetramethyl-4-piperidinyl) sebacate 8: 395:. Additionally, it is a potent blocker of 103: 15: 638: 554: 544: 460:Alpert Reyes, Emily (16 September 2024). 180: 356: 352: 348: 344: 474:from the original on 16 September 2024. 416: 225: 200: 138: 207:Key: XITRBUPOXXBIJN-UHFFFAOYSA-N 7: 619:The Open Medicinal Chemistry Journal 360:. It is a white crystalline powder. 151: 14: 393:nicotinic acetylcholine receptors 261: 255: 22: 339:hindered amine light stabilizer 315:(at 25 °C , 100 kPa). 580:Forensic Science International 387:Potential medical significance 267: 249: 1: 592:10.1016/s0379-0738(00)00462-x 391:It is capable of inhibiting 631:10.2174/1874104501812010088 731: 341:with the chemical formula 309: 236: 216: 191: 43: 35: 30: 21: 429:pubchem.ncbi.nlm.nih.gov 401:calcium channel blockers 375:Its production involves 371:Production and reactions 546:10.1073/pnas.90.20.9523 397:L-type calcium channels 381:tetramethylpiperidinol 367:in the United States. 677:10.1093/toxsci/kfh025 403:, it can precipitate 285: g·mol 18: 705:Plastics additives 319:Infobox references 16: 488:. 13 August 2014. 468:Los Angeles Times 327:Chemical compound 325: 324: 85:Interactive image 722: 689: 688: 659: 653: 652: 642: 610: 604: 603: 575: 569: 568: 558: 548: 524: 518: 517: 496: 490: 489: 482: 476: 475: 465: 457: 451: 450: 439: 433: 432: 421: 359: 284: 269: 263: 257: 251: 244:Chemical formula 184: 164: 153: 142: 118: 107: 87: 63: 26: 19: 730: 729: 725: 724: 723: 721: 720: 719: 695: 694: 693: 692: 661: 660: 656: 612: 611: 607: 577: 576: 572: 526: 525: 521: 498: 497: 493: 484: 483: 479: 459: 458: 454: 441: 440: 436: 423: 422: 418: 413: 389: 373: 358: 354: 350: 346: 342: 333:(also known as 328: 321: 316: 282: 272: 266: 260: 254: 246: 232: 229: 224: 223: 212: 209: 208: 205: 199: 198: 187: 167: 154: 128: 110: 90: 77: 66: 53: 39: 12: 11: 5: 728: 726: 718: 717: 712: 707: 697: 696: 691: 690: 654: 605: 570: 539:(20): 9523–7. 519: 491: 477: 452: 434: 415: 414: 412: 409: 388: 385: 372: 369: 326: 323: 322: 317: 313:standard state 310: 307: 306: 303: 297: 296: 293: 287: 286: 280: 274: 273: 270: 264: 258: 252: 247: 242: 239: 238: 234: 233: 231: 230: 227: 219: 218: 217: 214: 213: 211: 210: 206: 203: 202: 194: 193: 192: 189: 188: 186: 185: 177: 175: 169: 168: 166: 165: 157: 155: 147: 144: 143: 136: 130: 129: 127: 126: 122: 120: 112: 111: 109: 108: 100: 98: 92: 91: 89: 88: 80: 78: 71: 68: 67: 65: 64: 56: 54: 49: 46: 45: 41: 40: 37: 33: 32: 28: 27: 13: 10: 9: 6: 4: 3: 2: 727: 716: 713: 711: 708: 706: 703: 702: 700: 686: 682: 678: 674: 671:(2): 368–74. 670: 666: 658: 655: 650: 646: 641: 636: 632: 628: 624: 620: 616: 609: 606: 601: 597: 593: 589: 585: 581: 574: 571: 566: 562: 557: 552: 547: 542: 538: 534: 530: 523: 520: 515: 511: 508:(2): 718–26. 507: 503: 495: 492: 487: 481: 478: 473: 469: 464: 456: 453: 448: 444: 438: 435: 430: 426: 420: 417: 410: 408: 406: 402: 398: 394: 386: 384: 382: 378: 370: 368: 366: 361: 340: 336: 332: 320: 314: 308: 304: 302: 301:Melting point 299: 298: 294: 292: 289: 288: 281: 279: 276: 275: 248: 245: 241: 240: 235: 226: 222: 215: 201: 197: 190: 183: 179: 178: 176: 174: 171: 170: 163: 159: 158: 156: 150: 146: 145: 141: 137: 135: 132: 131: 124: 123: 121: 119: 114: 113: 106: 102: 101: 99: 97: 94: 93: 86: 82: 81: 79: 75: 70: 69: 62: 58: 57: 55: 52: 48: 47: 42: 34: 29: 25: 20: 668: 664: 657: 622: 618: 608: 586:(3): 322–7. 583: 579: 573: 536: 532: 522: 505: 501: 494: 480: 467: 455: 446: 437: 428: 419: 390: 377:sebacic acid 374: 362: 334: 330: 329: 44:Identifiers 36:Other names 710:Piperidines 335:Tinuvin 770 237:Properties 699:Categories 411:References 405:adrenergic 295:1.05 g/cm 278:Molar mass 182:6803A71201 96:ChemSpider 72:3D model ( 61:52829-07-9 51:CAS Number 625:: 88–97. 407:release. 125:258-207-9 117:EC Number 685:14657520 649:30288180 600:11390147 472:Archived 365:fentanyl 640:6142673 565:8415734 514:8113983 443:"BTMPS" 337:) is a 291:Density 283:480.734 149:PubChem 140:C083752 715:Esters 683:  647:  637:  598:  563:  553:  512:  221:SMILES 162:164282 105:144046 31:Names 17:BTMPS 556:47601 331:BTMPS 196:InChI 74:JSmol 681:PMID 645:PMID 596:PMID 561:PMID 510:PMID 379:and 173:UNII 134:MeSH 673:doi 635:PMC 627:doi 588:doi 584:119 551:PMC 541:doi 506:268 152:CID 701:: 679:. 669:77 667:. 643:. 633:. 623:12 621:. 617:. 594:. 582:. 559:. 549:. 537:90 535:. 531:. 504:. 470:. 466:. 445:. 427:. 383:. 349:52 345:28 259:52 253:28 687:. 675:: 651:. 629:: 602:. 590:: 567:. 543:: 516:. 449:. 431:. 357:4 355:O 353:2 351:N 347:H 343:C 271:4 268:O 265:2 262:N 256:H 250:C 76:)

Index


CAS Number
52829-07-9
JSmol
Interactive image
ChemSpider
144046
EC Number
MeSH
C083752
PubChem
164282
UNII
6803A71201
InChI
SMILES
Chemical formula
Molar mass
Density
Melting point
standard state
Infobox references
hindered amine light stabilizer
fentanyl
sebacic acid
tetramethylpiperidinol
nicotinic acetylcholine receptors
L-type calcium channels
calcium channel blockers
adrenergic

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