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p-Dimethylaminocinnamaldehyde

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A new colourimetric assay for flavonoids in pilsner beers. Jan A. Delcour and Didier Janssens de Varebeke, Journal of the Institute of Brewing, January–February 1985, Volume 91, Issue 1, pages 37–40,
869:"The van URK-Salkowski reagent — a sensitive and specific chromogenic reagent for silica gel thin-layer chromatographic detection and identification of indole derivatives" 783:
Glavnik, V.; Simonovska, B.; Vovk, I. (2009). "Densitometric determination of (+)-catechin and (−)-epicatechin by 4-dimethylaminocinnamaldehyde reagent".
820:"Studies on the Oxidation of Indole-3-Acetic Acid by Peroxidase Enzymes. I. Colorimetric Determination of Indole-3-Acetic Acid Oxidation Products" 740:
Li, Y. G.; Tanner, G.; Larkin, P. (1996). "TheDMACA-HCl Protocol and the Threshold Proanthocyanidin Content for Bloat Safety in Forage Legumes".
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The DMACA reagent changes color over several days when exposed to air but when refrigerated can be stored for up to two weeks.
652:"Indole derivatives produced by the fungusColletotrichum acutatumcausing lime anthracnose and postbloom fruit drop of citrus" 198: 523:
compounds in plants, resulting in a blue staining. It has been used for grapevine fruit or for legumes foliage histology.
579:"P-Dimethylaminocinnamaldehyde derivatization for colorimetric detection and HPLC–UV/vis–MS/MS identification of indoles" 312: 456: 936: 926: 693:"The Grapevine Transcription Factor VvMYBPA1 Regulates Proanthocyanidin Synthesis during Fruit Development" 255: 627: 276: 515:, particularly for production in cells. It is used for the rapid identification of bacteria containing 868: 174: 293: 192: 946: 151: 139: 39: 538:
procedure. The DMACA reagent may be superior to the vanillin procedure for the detection of
557: 264: 163: 75: 8: 297: 65: 941: 844: 819: 771: 717: 692: 603: 578: 119: 887: 668: 651: 931: 891: 849: 800: 722: 673: 608: 495: 232: 220: 883: 839: 831: 792: 767: 749: 712: 704: 663: 598: 590: 520: 370: 478:) is an aromatic hydrocarbon. It is used in an acidic solution to detect indoles. 244: 796: 502: 911: 450: 594: 26: 920: 691:
Bogs, J.; Jaffe, F. W.; Takos, A. M.; Walker, A. R.; Robinson, S. P. (2007).
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Chung, K. R.; Shilts, T.; Ertürk, Ã. M.; Timmer, L. W.; Ueng, P. P. (2003).
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A colorimetric assay based upon the reaction of A-rings with the chromogen.
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10.1002/(SICI)1097-0010(199601)70:1<89::AID-JSFA470>3.0.CO;2-N
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The DMACA reagent may also be referred to as the Renz and Loew reagent.
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InChI=1S/C11H13NO/c1-12(2)11-7-5-10(6-8-11)4-3-9-13/h3-9H,1-2H3/b4-3+
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Except where otherwise noted, data are given for materials in their
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InChI=1/C11H13NO/c1-12(2)11-7-5-10(6-8-11)4-3-9-13/h3-9H,1-2H3/b4-3+
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enzyme systems. It is also particularly useful for localization of
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The DMACA is any of a number of acidified DMACA solutions:
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It is primarily used as a histological dye used to detect
560:, a simple spot-test to presumptively identify alkaloids 649: 782: 576: 690: 530:-Dimethylaminocinnamaldehyde has been developed for 501:1 g DMACA, 1 mL conc. hydrochloric acid and 99 mL 625: 918: 243: 231: 219: 74: 742:Journal of the Science of Food and Agriculture 739: 577:Porubsky, P.; Scott, E.; Williams, T. (2008). 817: 507:1 g DMACA in 99 mL conc. hydrochloric acid. 481: 296: 162: 150: 138: 843: 716: 667: 602: 263: 583:Archives of Biochemistry and Biophysics 292: 197: 919: 866: 534:in beer that can be compared with the 432:329 °C (624 °F; 602 K) 422:138 °C (280 °F; 411 K) 402:white to light yellow crystal powder 324:Key: RUKJCCIJLIMGEP-ONEGZZNKSA-N 818:Meudt, W. J.; Gaines, T. P. (1967). 619: 334:Key: RUKJCCIJLIMGEP-ONEGZZNKBZ 210: 13: 772:10.1002/j.2050-0416.1985.tb04303.x 14: 958: 905: 628:"DMACA Reagent for microbiology" 25: 453:(at 25 °C , 100 kPa). 860: 776: 760: 733: 684: 570: 498:and diluted to 50mL with water 1: 888:10.1016/S0021-9673(00)89300-0 669:10.1016/S0378-1097(03)00605-0 564: 199:4-Dimethylaminocinnamaldehyde 53:4-Dimethylaminocinnamaldehyde 20:-Dimethylaminocinnamaldehyde 797:10.1016/j.chroma.2009.03.026 472:-Dimethylaminocinnamaldehyde 7: 876:Journal of Chromatography A 785:Journal of Chromatography A 551: 490:0.117 g of DMACA, 39 mL of 10: 963: 394:175.22 g/mol 355:C(=O)C=CC1=CC=C(C=C1)N(C)C 656:FEMS Microbiology Letters 595:10.1016/j.abb.2008.03.035 447: 363: 343: 308: 58: 48: 38: 33: 24: 482:Use as a testing reagent 626:Sigma-Aldrich Co. LLC. 937:Drug testing reagents 836:10.1104/pp.42.10.1395 709:10.1104/pp.106.093203 927:Conjugated aldehydes 912:DMACA on www.bd.com 867:Ehmann, A. (1977). 120:Beilstein Reference 21: 457:Infobox references 16: 558:Ehrlich's reagent 521:proanthocyanidins 496:hydrochloric acid 465:Chemical compound 463: 462: 277:CompTox Dashboard 100:Interactive image 954: 900: 899: 873: 864: 858: 857: 847: 824:Plant Physiology 815: 809: 808: 780: 774: 764: 758: 757: 737: 731: 730: 720: 703:(3): 1347–1361. 697:Plant Physiology 688: 682: 681: 671: 647: 638: 637: 635: 634: 623: 617: 616: 606: 574: 371:Chemical formula 301: 300: 285: 283: 267: 247: 235: 223: 212: 201: 177: 166: 154: 142: 102: 78: 29: 22: 15: 962: 961: 957: 956: 955: 953: 952: 951: 917: 916: 908: 903: 871: 865: 861: 816: 812: 791:(20): 4485–91. 781: 777: 765: 761: 738: 734: 689: 685: 648: 641: 632: 630: 624: 620: 575: 571: 567: 554: 494:, 5 mL of conc 484: 466: 459: 454: 383: 379: 373: 359: 356: 351: 350: 339: 336: 335: 332: 326: 325: 322: 316: 315: 304: 286: 279: 270: 250: 213: 187: 169: 122: 105: 92: 81: 68: 54: 52: 44: 12: 11: 5: 960: 950: 949: 944: 939: 934: 929: 915: 914: 907: 906:External links 904: 902: 901: 882:(2): 267–276. 859: 830:(10): 1395–9. 810: 775: 759: 732: 683: 639: 618: 568: 566: 563: 562: 561: 553: 550: 509: 508: 505: 499: 483: 480: 464: 461: 460: 455: 451:standard state 448: 445: 444: 441: 434: 433: 430: 424: 423: 420: 414: 413: 410: 404: 403: 400: 396: 395: 392: 386: 385: 381: 377: 374: 369: 366: 365: 361: 360: 358: 357: 354: 346: 345: 344: 341: 340: 338: 337: 333: 330: 329: 327: 323: 320: 319: 311: 310: 309: 306: 305: 303: 302: 289: 287: 275: 272: 271: 269: 268: 260: 258: 252: 251: 249: 248: 241: 229: 216: 214: 206: 203: 202: 195: 189: 188: 186: 185: 181: 179: 171: 170: 168: 167: 160: 148: 135: 133: 127: 126: 123: 118: 115: 114: 111: 110:Abbreviations 107: 106: 104: 103: 95: 93: 86: 83: 82: 80: 79: 71: 69: 64: 61: 60: 56: 55: 50: 46: 45: 42: 36: 35: 31: 30: 9: 6: 4: 3: 2: 959: 948: 947:Staining dyes 945: 943: 940: 938: 935: 933: 930: 928: 925: 924: 922: 913: 910: 909: 897: 893: 889: 885: 881: 877: 870: 863: 855: 851: 846: 841: 837: 833: 829: 825: 821: 814: 806: 802: 798: 794: 790: 786: 779: 773: 769: 763: 755: 751: 747: 743: 736: 728: 724: 719: 714: 710: 706: 702: 698: 694: 687: 679: 675: 670: 665: 661: 657: 653: 646: 644: 629: 622: 614: 610: 605: 600: 596: 592: 588: 584: 580: 573: 569: 559: 556: 555: 549: 546: 543: 541: 537: 533: 529: 524: 522: 518: 517:tryptophanase 514: 506: 504: 500: 497: 493: 489: 488: 487: 479: 477: 473: 471: 458: 452: 446: 442: 439: 436: 435: 431: 429: 428:Boiling point 426: 425: 421: 419: 418:Melting point 416: 415: 411: 409: 406: 405: 401: 398: 397: 393: 391: 388: 387: 375: 372: 368: 367: 362: 353: 352: 349: 342: 328: 318: 317: 314: 307: 299: 295: 294:DTXSID9022237 291: 290: 288: 278: 274: 273: 266: 262: 261: 259: 257: 254: 253: 246: 242: 239: 234: 230: 227: 222: 218: 217: 215: 209: 205: 204: 200: 196: 194: 191: 190: 183: 182: 180: 178: 173: 172: 165: 161: 158: 153: 149: 146: 141: 137: 136: 134: 132: 129: 128: 124: 121: 117: 116: 112: 109: 108: 101: 97: 96: 94: 90: 85: 84: 77: 73: 72: 70: 67: 63: 62: 57: 47: 43:3-prop-2-enal 41: 37: 32: 28: 23: 19: 879: 875: 862: 827: 823: 813: 788: 784: 778: 762: 745: 741: 735: 700: 696: 686: 662:(1): 23–30. 659: 655: 631:. Retrieved 621: 589:(1): 14–17. 586: 582: 572: 547: 544: 527: 525: 510: 485: 475: 469: 468: 467: 237: 225: 156: 144: 59:Identifiers 49:Other names 17: 440:in dioxane 412:1.057 g/mL 399:Appearance 364:Properties 921:Categories 748:: 89–101. 633:2013-10-29 565:References 532:flavanoids 438:Solubility 390:Molar mass 265:9RSI7WZ9F0 131:ChemSpider 87:3D model ( 76:20432-35-3 66:CAS Number 40:IUPAC name 942:Histology 540:catechins 384:NO 184:228-267-0 176:EC Number 932:Anilines 854:16656668 805:19339019 727:17208963 678:13129603 613:18423367 552:See also 536:vanillin 233:25310830 152:23646677 845:1086736 718:1820911 604:2504418 513:indoles 492:ethanol 443:50 g/L 408:Density 236: ( 224: ( 221:5284506 208:PubChem 155: ( 143: ( 140:4447567 125:972369 896:188858 894:  852:  842:  803:  725:  715:  676:  611:  601:  348:SMILES 113:DMACA 34:Names 872:(PDF) 503:water 476:DMACA 313:InChI 245:92224 164:83262 89:JSmol 892:PMID 850:PMID 801:PMID 789:1216 723:PMID 674:PMID 609:PMID 256:UNII 193:MeSH 51:DMAC 884:doi 880:132 840:PMC 832:doi 793:doi 768:doi 750:doi 713:PMC 705:doi 701:143 664:doi 660:226 599:PMC 591:doi 587:475 282:EPA 211:CID 923:: 890:. 878:. 874:. 848:. 838:. 828:42 826:. 822:. 799:. 787:. 746:70 744:. 721:. 711:. 699:. 695:. 672:. 658:. 654:. 642:^ 607:. 597:. 585:. 581:. 542:. 382:13 378:11 898:. 886:: 856:. 834:: 807:. 795:: 770:: 756:. 752:: 729:. 707:: 680:. 666:: 636:. 615:. 593:: 528:p 474:( 470:p 380:H 376:C 284:) 280:( 240:) 238:Z 228:) 226:E 159:) 157:Z 147:) 145:E 91:) 18:p

Index


IUPAC name
CAS Number
20432-35-3
JSmol
Interactive image
Beilstein Reference
ChemSpider
4447567
23646677
83262
EC Number
MeSH
4-Dimethylaminocinnamaldehyde
PubChem
5284506
25310830
92224
UNII
9RSI7WZ9F0
CompTox Dashboard
DTXSID9022237
Edit this at Wikidata
InChI
SMILES
Chemical formula
Molar mass
Density
Melting point
Boiling point

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