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MedKoo Cat#: 591969 | Name: Isoeugenol
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Description:

WARNING: This product is for research use only, not for human or veterinary use.

Isoeugenol is used in Enucleation in a Cownose Ray.

Chemical Structure

Isoeugenol
Isoeugenol
CAS#97-54-1

Theoretical Analysis

MedKoo Cat#: 591969

Name: Isoeugenol

CAS#: 97-54-1

Chemical Formula: C10H12O2

Exact Mass: 164.0837

Molecular Weight: 164.20

Elemental Analysis: C, 73.15; H, 7.37; O, 19.49

Price and Availability

Size Price Availability Quantity
5g USD 250.00 2 Weeks
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Related CAS #
No Data
Synonym
Isoeugenol; (E)-Isoeugenol; trans-Isoeugenol; Iso-eugenol; NSC 6769; NSC6769; NSC-6769
IUPAC/Chemical Name
Phenol, 2-methoxy-4-(1-propen-1-yl)-
InChi Key
BJIOGJUNALELMI-ONEGZZNKSA-N
InChi Code
InChI=1S/C10H12O2/c1-3-4-8-5-6-9(11)10(7-8)12-2/h3-7,11H,1-2H3/b4-3+
SMILES Code
OC1=CC=C(/C=C/C)C=C1OC
Appearance
Liquid
Purity
>97% (cis- and trans- mixture)
Shipping Condition
Shipped under ambient temperature as non-hazardous chemical. This product is stable enough for a few weeks during ordinary shipping and time spent in Customs.
Storage Condition
Dry, dark and at 0 - 4 C for short term (days to weeks) or -20 C for long term (months to years).
Solubility
Soluble in DMSO
Shelf Life
>3 years if stored properly
Drug Formulation
This drug may be formulated in DMSO
Stock Solution Storage
0 - 4 C for short term (days to weeks), or -20 C for long term (months).
HS Tariff Code
2934.99.03.00
More Info

Preparing Stock Solutions

The following data is based on the product molecular weight 164.20 Batch specific molecular weights may vary from batch to batch due to the degree of hydration, which will affect the solvent volumes required to prepare stock solutions.

Recalculate based on batch purity %
Concentration / Solvent Volume / Mass 1 mg 5 mg 10 mg
1 mM 1.15 mL 5.76 mL 11.51 mL
5 mM 0.23 mL 1.15 mL 2.3 mL
10 mM 0.12 mL 0.58 mL 1.15 mL
50 mM 0.02 mL 0.12 mL 0.23 mL
1: Abraham Gabriel A, Yee-Nin ST, Adamu L, Hassan HMD, Wahid AH. Enucleation in a Cownose Ray (Rhinoptera bonasus). Case Rep Vet Med. 2018 Mar 19;2018:5048948. doi: 10.1155/2018/5048948. eCollection 2018. PubMed PMID: 29955436; PubMed Central PMCID: PMC6005293. 2: Tang J, Shi L, Li L, Long L, Ding S. Expression and characterization of a 9-cis-epoxycarotenoid dioxygenase from Serratia sp. ATCC 39006 capable of biotransforming isoeugenol and 4-vinylguaiacol to vanillin. Biotechnol Rep (Amst). 2018 Apr 18;18:e00253. doi: 10.1016/j.btre.2018.e00253. eCollection 2018 Jun. PubMed PMID: 29881703; PubMed Central PMCID: PMC5989660. 3: Shormanov VK, Tsatsua EP, Astashkina AP, Vorob'eva OA, Mastikhina YA. [The peculiar features of the distribution of 2-metoxy-4-(1-propenyl)-hydroxybenzene in the organism of the warm-blooded animals]. Sud Med Ekspert. 2018;61(3):35-39. doi: 10.17116/sudmed201861335-39. Russian. PubMed PMID: 29863718. 4: McQuate GT, Royer JE, Sylva CD. Field Trapping Bactrocera latifrons (Diptera: Tephritidae) with Select Eugenol Analogs That Have Been Found to Attract Other 'Non-Responsive' Fruit Fly Species. Insects. 2018 May 1;9(2). pii: E50. doi: 10.3390/insects9020050. PubMed PMID: 29723960. 5: Ruiz-Moreno MJ, Raposo R, Puertas B, Cuevas FJ, Chinnici F, Moreno-Rojas JM, Cantos-Villar E. Effect of a grapevine-shoot waste extract on red wine aromatic properties. J Sci Food Agric. 2018 Apr 26. doi: 10.1002/jsfa.9104. [Epub ahead of print] PubMed PMID: 29696658. 6: Ostovar S, Franco A, Puente-Santiago AR, Pinilla-de Dios M, Rodríguez-Padrón D, Shaterian HR, Luque R. Efficient Mechanochemical Bifunctional Nanocatalysts for the Conversion of Isoeugenol to Vanillin. Front Chem. 2018 Apr 3;6:77. doi: 10.3389/fchem.2018.00077. eCollection 2018. PubMed PMID: 29666790; PubMed Central PMCID: PMC5891640. 7: Royer JE, Khan M, Mayer DG. Methyl-isoeugenol, a Highly Attractive Male Lure for the Cucurbit Flower Pest Zeugodacus diversus (Coquillett) (syn. Bactrocera diversa) (Diptera: Tephritidae: Dacinae). J Econ Entomol. 2018 May 28;111(3):1197-1201. doi: 10.1093/jee/toy068. PubMed PMID: 29618022. 8: Sharma V, Amarnath N, Shukla S, Ayana R, Kumar N, Yadav N, Kannan D, Sehrawat S, Pati S, Lochab B, Singh S. Benzoxazine derivatives of phytophenols show anti-plasmodial activity via sodium homeostasis disruption. Bioorg Med Chem Lett. 2018 May 15;28(9):1629-1637. doi: 10.1016/j.bmcl.2018.03.047. Epub 2018 Mar 19. PubMed PMID: 29615339. 9: Saha S, Verma RJ. Molecular interactions of active constituents of essential oils in zwitterionic lipid bilayers. Chem Phys Lipids. 2018 Jul;213:76-87. doi: 10.1016/j.chemphyslip.2018.03.008. Epub 2018 Mar 27. PubMed PMID: 29596800. 10: Ogawa K, Tashima A, Sadakata M, Morinaga O. Appetite-enhancing effects of vanilla flavours such as vanillin. J Nat Med. 2018 Jun;72(3):798-802. doi: 10.1007/s11418-018-1206-x. Epub 2018 Mar 22. PubMed PMID: 29569223. 11: Rahman A, Rahman M, Demirtas I. Chemical Composition and Antioxidant Potential of Essential Oil and Organic Extracts of Euphorbia tithymaloides L. from Kushtia Region. Anticancer Agents Med Chem. 2018 Feb 28. doi: 10.2174/1871520618666180228122318. [Epub ahead of print] PubMed PMID: 29493467. 12: Yamamoto T, Riehl B, Naba K, Nakahara K, Wiebe A, Saitoh T, Waldvogel SR, Einaga Y. A solvent-directed stereoselective and electrocatalytic synthesis of diisoeugenol. Chem Commun (Camb). 2018 Mar 13;54(22):2771-2773. doi: 10.1039/c8cc00794b. PubMed PMID: 29484329. 13: Ali A, Chong CH, Mah SH, Abdullah LC, Choong TSY, Chua BL. Impact of Storage Conditions on the Stability of Predominant Phenolic Constituents and Antioxidant Activity of Dried Piper betle Extracts. Molecules. 2018 Feb 23;23(2). pii: E484. doi: 10.3390/molecules23020484. PubMed PMID: 29473847. 14: Tarazona A, Gómez JV, Gavara R, Mateo-Castro R, Gimeno-Adelantado JV, Jiménez M, Mateo EM. Risk management of ochratoxigenic fungi and ochratoxin A in maize grains by bioactive EVOH films containing individual components of some essential oils. Int J Food Microbiol. 2018 Mar 23;269:107-119. doi: 10.1016/j.ijfoodmicro.2018.02.002. Epub 2018 Feb 3. PubMed PMID: 29421354. 15: Marquez-Medina MD, Prinsen P, Li H, Shih K, Romero AA, Luque R. Continuous-Flow Synthesis of Supported Magnetic Iron Oxide Nanoparticles for Efficient Isoeugenol Conversion into Vanillin. ChemSusChem. 2018 Jan 23;11(2):389-396. doi: 10.1002/cssc.201701884. Epub 2017 Dec 28. PubMed PMID: 29161467. 16: Nielsen CK, Subbiahdoss G, Zeng G, Salmi Z, Kjems J, Mygind T, Snabe T, Meyer RL. Antibacterial isoeugenol coating on stainless steel and polyethylene surfaces prevents biofilm growth. J Appl Microbiol. 2018 Jan;124(1):179-187. doi: 10.1111/jam.13634. Epub 2017 Dec 18. PubMed PMID: 29119696. 17: Parki A, Chaubey P, Prakash O, Kumar R, Pant AK. Seasonal Variation in Essential Oil Compositions and Antioxidant Properties of Acorus calamus L. Accessions. Medicines (Basel). 2017 Nov 8;4(4). pii: E81. doi: 10.3390/medicines4040081. PubMed PMID: 29117116; PubMed Central PMCID: PMC5750605. 18: Ashengroph M, Amini J. Bioconversion of isoeugenol to vanillin and vanillic acid using the resting cells of Trichosporon asahii. 3 Biotech. 2017 Dec;7(6):358. doi: 10.1007/s13205-017-0998-9. Epub 2017 Oct 3. PubMed PMID: 28979831; PubMed Central PMCID: PMC5626669. 19: Pavela R, Maggi F, Lupidi G, Mbuntcha H, Woguem V, Womeni HM, Barboni L, Tapondjou LA, Benelli G. Clausena anisata and Dysphania ambrosioides essential oils: from ethno-medicine to modern uses as effective insecticides. Environ Sci Pollut Res Int. 2018 Apr;25(11):10493-10503. doi: 10.1007/s11356-017-0267-9. Epub 2017 Oct 1. PubMed PMID: 28965298. 20: Chance RJ, Allcock Z, Secombes CJ, Collet B, Collins C. Effect of repeated exposure to AQUI-S(®) on the viability and growth of Neoparamoeba perurans. J Fish Dis. 2018 Feb;41(2):291-298. doi: 10.1111/jfd.12712. Epub 2017 Sep 25. PubMed PMID: 28944485; PubMed Central PMCID: PMC5813168.

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