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442:, a chemical compound most frequently used in cosmetics as a fragrance additive or UV light absorber. It appears as an almost colorless liquid with a mild odor described as "very faint, sweet-floral, slightly balsamic" by some, while others smell nothing at all. There is debate whether the odour is caused solely by impurities or a genetic predisposition. It occurs naturally in a variety of plants and plant extracts and is widely used in blends of fragrance materials.
397:
541:"Toxicologic and Dermatologic Assessments for Three Groups of Fragrance Ingredients: 1) Related Esters and Alcohols of Cinnamic Acid and Cinnamic Alcohol, 2) Ionones, 3) Salicylates"
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There is some evidence that people may become sensitized to this material and as a result, there is a restriction standard concerning the use of this material in fragrances by the
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Belsito, D; Bickers, D; Bruze, M; Calow, P; Greim, H; Hanifin, JM; Rogers, AE; Saurat, JH; Sipes, IG; Tagami, H (2007).
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InChI=1S/C14H12O3/c15-13-9-5-4-8-12(13)14(16)17-10-11-6-2-1-3-7-11/h1-9,15H,10H2
268:
InChI=1/C14H12O3/c15-13-9-5-4-8-12(13)14(16)17-10-11-6-2-1-3-7-11/h1-9,15H,10H2
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An
Introduction to Perfumery by Curtis & Williams 2nd Edition, 2009,
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Except where otherwise noted, data are given for materials in their
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24 to 25 °C (75 to 77 °F; 297 to 298 K)
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381:318 °C (604 °F; 591 K)
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649:Consumer Product Information Database
261:Key: ZCTQGTTXIYCGGC-UHFFFAOYSA-N
116:
7:
600:International Fragrance Association
447:International Fragrance Association
271:Key: ZCTQGTTXIYCGGC-UHFFFAOYAC
171:
14:
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391:(at 25 °C , 100 kPa).
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1:
548:Food and Chemical Toxicology
464:in floral perfumes such as
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528:. The Good Scents Company.
456:for crystalline synthetic
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560:10.1016/j.fct.2007.09.087
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292:O=C(OCc1ccccc1)c2ccccc2O
50:Benzyl 2-hydroxybenzoate
786:2-Ethylhexyl salicylate
554:(Supplement 1): S1-23.
460:and as a component and
596:"Standards Restricted"
781:Salicylmethylecgonine
731:Bismuth subsalicylate
806:Potassium salicylate
771:Trolamine salicylate
726:Isopropyl salicylate
716:Magnesium salicylate
46:Preferred IUPAC name
526:"Benzyl salicylate"
343: g·mol
18:
490:Oil of wintergreen
418:Infobox references
17:Benzyl salicylate
16:
827:Salicylate esters
814:
813:
801:Copper aspirinate
796:Benzyl salicylate
736:Sodium salicylate
711:Methyl salicylate
645:Benzyl salicylate
630:978-1-870228-24-4
622:978-0-9608752-8-3
452:It is used as a
430:Benzyl salicylate
426:Chemical compound
424:
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351:Colorless liquid
214:CompTox Dashboard
98:Interactive image
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721:Ethyl salicylate
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602:. Archived from
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741:Salicylamide
612:
604:the original
590:
579:. Retrieved
572:the original
551:
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520:
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451:
444:
429:
428:
118:ChEMBL460124
57:Identifiers
761:Ethenzamide
685:Salicylates
348:Appearance
301:Properties
156:100.003.876
821:Categories
776:Homosalate
766:Diflunisal
751:Benorilate
581:2012-04-05
496:References
478:wallflower
361:1.17 g/cm
336:Molar mass
202:WAO5MNK9TU
129:ChemSpider
85:3D model (
64:CAS Number
756:Salsalate
706:Aloxiprin
466:carnation
791:Aluminon
568:18035463
484:See also
462:fixative
74:118-58-1
746:Salicin
701:Aspirin
647:in the
470:jasmine
454:solvent
411:what is
409: (
357:Density
341:228.247
169:PubChem
628:
620:
566:
512:
476:, and
437:benzyl
406:verify
403:
285:SMILES
109:ChEMBL
40:Names
575:(PDF)
544:(PDF)
474:lilac
458:musks
440:ester
432:is a
250:InChI
87:JSmol
626:ISBN
618:ISBN
564:PMID
510:ISBN
193:UNII
182:8363
138:8060
556:doi
219:EPA
172:CID
823::
624:,
598:.
562:.
552:45
550:.
546:.
480:.
472:,
468:,
449:.
323:12
317:14
677:e
670:t
663:v
584:.
558::
401:N
329:3
326:O
320:H
314:C
221:)
217:(
89:)
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