385:
244:
899:
688:
683:
678:
43:
895:
34:
900:
1092:
898:
696:
658:
916:
818:
1490:
1468:
985:
1105:
810:
901:
434:
1745:
Betz, Oliver (2010). "Adhesive
Exocrine Glands in Insects: Morphology, Ultrastructure, and Adhesive Secretion". In von Byern, Janek; Grunwald, Ingo (eds.).
814:
923:
770:
1770:
1526:
1150:(OH). It is a colourless, viscous liquid that is used as an intermediate in the production of other chemicals. It is a derivative of
1293:-cresol to form a polyaniline film with a superior conductivity than polyaniline alone. This phenomenon is known as secondary doping.
1593:
1566:
399:
653:
May cause serious burns. Very destructive of mucous membranes. Harmful if inhaled. Toxic in contact with the skin or if swallowed.
639:
790:
1112:
766:
1612:). Jack Adams, Alexander Garcia and Christopher S. Foote, Journal of Chemical Ecology, 1978, Volume 4, Number 1, 17-25,
798:
756:
342:
687:
1702:
363:
909:
1815:
1009:
996:
744:
251:
42:
740:
1629:
Talhout, Reinskje; Schulz, Thomas; Florek, Ewa; Van
Benthem, Jan; Wester, Piet; Opperhuizen, Antoon (2011).
834:
802:
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826:
677:
239:
822:
181:
710:
682:
670:
55:
1794:
854:
1418:
830:
782:
380:
129:
95:
1727:
1356:
1221:
866:
141:
838:
774:
1754:
1766:
1719:
1670:
1652:
1589:
1562:
1556:
1522:
1374:
1034:
794:
201:
17:
1608:
Some chemical constituents of the secretion from the temporal gland of the
African elephant (
1311:, an important synthetic chemical for regions lacking natural sources of the flavor compound:
1810:
1758:
1746:
1711:
1660:
1642:
1613:
1514:
1393:
1135:
862:
600:
525:
457:
842:
351:
1304:
1229:
1189:
945:
846:
806:
270:
1715:
105:
1040:
858:
384:
243:
161:
1665:
1630:
1272:
1213:
1083:
762:
728:
570:
1804:
1747:
1407:
1217:
558:
514:
504:
232:
33:
1731:
874:
1689:
1360:
1248:
778:
625:
1541:
Alan G. MacDiarmid and Arthur J. Epstein. 1995. "Secondary Doping in
Polyaniline"
1583:
786:
1762:
1286:
1262:
1185:
969:
935:
315:
1788:
1464:
1423:
1366:
1268:
1243:-Cresol is a precursor to numerous compounds. Important applications include:
554:
538:
476:
192:
1656:
1518:
1482:
1688:
Jones, T. H.; Clark, D. A.; Edwards, A. A.; Davidson, D. W.; Spande, T. F.;
1370:
1258:
1225:
1205:
619:
1723:
1674:
732:
1647:
724:
1252:
1181:
1162:
1155:
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915:
908:
881:
563:
547:
212:
221:
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1278:
1201:
736:
542:
494:
302:
252:
1435:
1338:
1308:
1209:
1197:
1193:
1151:
1074:
1054:
748:
172:
1082:
Except where otherwise noted, data are given for materials in their
290:
1389:
1388:-Cresol is a component found in temporal glands secretions during
720:
716:
326:
152:
128:
118:
1635:
International
Journal of Environmental Research and Public Health
1022:
870:
281:
1555:
Stroh, R.; Sydel, R.; Hahn, W. (1963). Foerst, Wilhelm (ed.).
1487:
Immediately
Dangerous to Life or Health Concentrations (IDLH)
850:
368:
893:
1558:
Newer
Methods of Preparative Organic Chemistry, Volume 2
1416:-Cresol is a component found in secretions from the ant
1212:, which can be oxidatively dealkylated analogous to the
1561:(1st ed.). New York: Academic Press. p. 344.
1184:, the volatile materials obtained in the production of
1100:
1585:
Industrial
Chemical Cresols and Downstream Derivatives
1491:
National
Institute for Occupational Safety and Health
1469:
National
Institute for Occupational Safety and Health
1192:. This residue contains a few percent by weight of
314:
897:
104:
1511:Ullmann's Encyclopedia of Industrial Chemistry
1509:Helmut Fiege (2007). "Cresols and Xylenols".
408:InChI=1S/C7H8O/c1-6-3-2-4-7(8)5-6/h2-5,8H,1H3
8:
519:202.8 °C (397.0 °F; 475.9 K)
418:InChI=1/C7H8O/c1-6-3-2-4-7(8)5-6/h2-5,8H,1H3
1692:(2004). "The chemistry of exploding ants,
383:
242:
200:
22:
1664:
1646:
1504:
1502:
1500:
350:
1588:. New York: CRC Press. pp. 99–100.
1463:NIOSH Pocket Guide to Chemical Hazards.
1180:-cresol is traditionally extracted from
1446:
439:
404:
379:
220:
1789:NIOSH Pocket Guide to Chemical Hazards
1631:"Hazardous Compounds in Tobacco Smoke"
1458:
1456:
1454:
1452:
1450:
233:
489:colorless liquid to yellowish liquid
411:Key: RLSSMJSEOOYNOY-UHFFFAOYSA-N
180:
160:
7:
1176:Together with many other compounds,
509:11 °C (52 °F; 284 K)
421:Key: RLSSMJSEOOYNOY-UHFFFAOYAJ
305:
289:
1716:10.1023/B:JOEC.0000042063.01424.28
14:
499:1.034 g/cm, liquid at 20 °C
1795:Chemical and physical properties
1582:Asim Kumar Mukhopadhyay (2004).
1200:. In the cymene–cresol process,
1090:
686:
681:
676:
41:
32:
1086:(at 25 °C , 100 kPa).
640:Occupational safety and health
1:
1265:to give 2,3,6-trimethylphenol
990:(US health exposure limits):
1406:-Cresol is a constituent of
978:2020 mg/kg (oral, rat, 1944)
533:5.8 g/100 ml at 100 °C
1763:10.1007/978-3-7091-0286-2_8
1749:Biological Adhesive Systems
1703:Journal of Chemical Ecology
1289:is cast from a solution of
1216:. Another method, involves
976:242 mg/kg (oral, rat, 1969)
958:or concentration (LD, LC):
531:2.35 g/100 ml at 20 °C
1832:
1483:"Cresol (o, m, p isomers)"
1303:the starting point in the
481:108.14 g/mol
15:
1080:
1046:
984:
954:
657:
637:
632:
450:
430:
395:
88:
81:1-Hydroxy-3-methylbenzene
64:
54:
49:
40:
31:
1519:10.1002/14356007.a08_025
980:828 mg/kg (oral, mouse)
757:Precautionary statements
16:Not to be confused with
1513:. Weinheim: Wiley-VCH.
582:Magnetic susceptibility
575:0.14 mmHg (20 °C)
1296:preservatives in some
1016:TWA 2.3 ppm (10 mg/m)
904:
1648:10.3390/ijerph8020613
1003:TWA 5 ppm (22 mg/m)
950:1.1%–? (149 °C)
903:
1419:Colobopsis saundersi
1154:and is an isomer of
886:(fire diamond)
1381:Natural occurrences
1247:pesticides such as
1228:in the presence of
1208:to give isomers of
1138:with the formula CH
526:Solubility in water
142:Beilstein Reference
28:
1618:10.1007/BF00988256
1610:Loxodonta africana
1398:Loxodonta africana
1222:methallyl chloride
1204:is alkylated with
1113:Infobox references
1047:Related compounds
1025:(Immediate danger)
905:
23:
1816:3-Tolyl compounds
1772:978-3-7091-0141-4
1394:African elephants
1190:(bituminous) coal
1121:Chemical compound
1119:
1118:
1035:Safety data sheet
711:Hazard statements
364:CompTox Dashboard
130:Interactive image
18:Metacresol purple
1823:
1797:chemicalbook.com
1777:
1776:
1752:
1742:
1736:
1735:
1710:(8): 1479–1492.
1690:Snelling, Roy R.
1685:
1679:
1678:
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1543:Synthetic Metals
1539:
1533:
1532:
1506:
1495:
1494:
1479:
1473:
1472:
1460:
1220:of a mixture of
1136:organic compound
1103:
1097:
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601:Refractive index
594:
592:
458:Chemical formula
388:
387:
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307:
293:
271:Gmelin Reference
254:
246:
235:
224:
204:
184:
164:
132:
108:
83:3-Methylbenzenol
74:3-Hydroxytoluene
45:
36:
29:
1831:
1830:
1826:
1825:
1824:
1822:
1821:
1820:
1801:
1800:
1785:
1780:
1773:
1744:
1743:
1739:
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1686:
1682:
1641:(12): 613–628.
1628:
1627:
1623:
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1383:
1346:
1342:
1335:
1331:
1325:
1321:
1305:total synthesis
1285:. For example,
1238:
1230:nickel carbonyl
1174:
1149:
1145:
1141:
1122:
1115:
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1109:
1108: ?)
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1783:External links
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1275:
1273:amylmetacresol
1266:
1255:
1237:
1234:
1214:cumene process
1173:
1170:
1147:
1143:
1139:
1132:3-methylphenol
1120:
1117:
1116:
1111:
1089:
1088:
1084:standard state
1081:
1078:
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59:3-methylphenol
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1365:synthesis of
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1355:synthesis of
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1218:carbonylation
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1199:
1196:and isomeric
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1041:External MSDS
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1024:
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1012:(Recommended)
1011:
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442:Cc1cc(O)ccc1
327:RTECS number
182:ChEMBL298312
89:Identifiers
76:
69:
65:Other names
24:
1753:. pp.
1700:complex)".
1698:cylindricus
1545:69 (85-92).
1357:dicresulene
1287:polyaniline
1269:antiseptics
1263:methylation
970:median dose
956:Lethal dose
936:Flash point
697:Signal word
643:(OHS/OSH):
486:Appearance
451:Properties
240:100.003.253
162:CHEBI:17231
1805:Categories
1694:Camponotus
1442:References
1424:Autothysis
1367:toliprolol
1271:, such as
1257:synthetic
1172:Production
671:Pictograms
555:Solubility
539:Solubility
477:Molar mass
352:GGO4Y809LO
193:ChemSpider
117:3D model (
96:CAS Number
56:IUPAC name
1657:1660-4601
1371:tolamolol
1259:vitamin E
1226:acetylene
1206:propylene
867:P403+P235
863:P370+P378
827:P308+P313
823:P307+P311
815:P304+P340
807:P302+P352
799:P301+P310
662:labelling
620:Viscosity
334:GO6125000
253:EC Number
1732:23756265
1724:15537154
1675:21556207
1493:(NIOSH).
1471:(NIOSH).
1430:See also
1392:in male
1375:cresatin
1283:polymers
1253:fenthion
1182:coal tar
1134:, is an
1053:Related
1029:250 ppm
883:NFPA 704
633:Hazards
584:(χ)
564:miscible
548:miscible
471:O
261:203-39-4
213:DrugBank
202:21105871
106:108-39-4
67:3-Cresol
27:-Cresol
1811:Cresols
1791:cdc.gov
1666:3084482
1465:"#0155"
1422:during
1298:insulin
1279:solvent
1202:toluene
1198:cresols
1166:-cresol
1159:-cresol
1130:, also
1128:-Cresol
1106:what is
1104: (
1071:-cresol
1064:-cresol
1055:phenols
614:1.5398
543:ethanol
495:Density
303:PubChem
276:101411
222:DB01776
147:506719
72:-Cresol
1769:
1757:–152.
1730:
1722:
1696:spp. (
1673:
1663:
1655:
1592:
1565:
1525:
1436:Cresol
1373:&
1309:thymol
1210:cymene
1194:phenol
1152:phenol
1101:verify
1098:
1075:phenol
1037:(SDS)
940:86 °C
703:Danger
589:−72.02
435:SMILES
291:C01467
173:ChEMBL
50:Names
1728:S2CID
1390:musth
1188:from
987:NIOSH
400:InChI
153:ChEBI
119:JSmol
1767:ISBN
1720:PMID
1671:PMID
1653:ISSN
1590:ISBN
1563:ISBN
1523:ISBN
1359:and
1326:O +
1281:for
1251:and
1224:and
1186:coke
1161:and
1126:meta
1023:IDLH
875:P501
871:P405
859:P363
855:P361
851:P330
847:P322
843:P321
839:P314
835:P312
831:P310
795:P281
791:P280
787:P273
783:P270
779:P264
775:P260
771:P210
767:P202
763:P201
749:H401
745:H373
741:H372
737:H370
733:H351
729:H314
725:H311
721:H301
717:H227
624:6.1
343:UNII
282:KEGG
1759:doi
1755:111
1712:doi
1661:PMC
1643:doi
1614:doi
1515:doi
1426:.
1400:).
1307:of
1261:by
1010:REL
997:PEL
660:GHS
557:in
541:in
369:EPA
316:342
306:CID
1807::
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