CAS Number607-91-0
Synonymsmyristicine; 4-methoxy-6-prop-2-en-1-yl-1,3-benzodioxole; 6-Allyl-4-methoxy-1,3-benzodioxole; MFCD00133549; Myristicin; 4-Méthoxy-6-(2-propèn-1-yl)-1,3-benzodioxole; 3-methoxy-4,5-methylenedioxyallylbenzene; 1-allyl-4,5-methylenedioxy-3-methoxybenzene; EINECS 210-146-9
Molecular FormulaC11H12O3
Molecular Weight192.21
Purity≥97.0 (GC)%
Density1.1±0.1 g/cm3
Boiling Point276.5±0.0 °C at 760 mmHg
Melting Point<-20ºC
Appearanceoil | clear, light yellow
EINECS210-146-9
Symbol
Signal WordWarning
| Chemical & Physical Properties | |
|---|---|
| CAS Number | 607-91-0 |
| Catalog No. | 2A-9024056 |
| Chinese Name | 肉豆蔻醚 |
| Synonyms | myristicine; 4-methoxy-6-prop-2-en-1-yl-1,3-benzodioxole; 6-Allyl-4-methoxy-1,3-benzodioxole; MFCD00133549; Myristicin; 4-Méthoxy-6-(2-propèn-1-yl)-1,3-benzodioxole; 3-methoxy-4,5-methylenedioxyallylbenzene; 1-allyl-4,5-methylenedioxy-3-methoxybenzene; EINECS 210-146-9 |
| Molecular Formula | C11H12O3 |
| Molecular Weight | 192.21 |
| Purity | ≥97.0 (GC) |
| Density | 1.1±0.1 g/cm3 |
| Boiling Point | 276.5±0.0 °C at 760 mmHg |
| Melting Point | <-20ºC |
| Appearance | oil | clear, light yellow |
| Storage Condition | Storage: Seal the container and store it in a seal |
| Application | Myristicine is a serotonin receptor antagonist and a weak monoamine oxidase (MAO) inhibitor. Myristicine is the main component of nutmeg essential oil. Myristicine abuse can produce hallucinogenic eff |
| EINECS | 210-146-9 |
| HTC | 2932999099 |
| PubChem ID | 329748745 |
| MDL Number | MFCD00133549 |
| SMILES | COc1cc(CC=C)cc2OCOc12 |
| InChI | 1S/C11H12O3/c1-3-4-8-5-9(12-2)11-10(6-8)13-7-14-11/h3,5-6H,1,4,7H2,2H3 |
| InChI Key | BNWJOHGLIBDBOB-UHFFFAOYSA-N |
| Beilstein/REAXYS | 166218 |
| NACRES Code | NA.24 |
| UNSPSC | 85151701 |
| Hazard Symbols | 9.0 |
| MSDS | msds/24056_1_607_91_0.pdf |
| Bioactivity | Myristicine act as a serotonin receptor antagonist, a weak monamine oxidase (MAO) inhibitor. Myristicine is the main component of nutmeg essential oil from Myristica fragrans Houtt. Myristicine abuse produce hallucinogenic effects, organ damage, deliriumand others[1]. Related Catalog Research Areas >> Neurological Disease Signaling Pathways >> GPCR/G Protein >> 5-HT Receptor Signaling Pathways >> Neuronal Signaling >> 5-HT Receptor References [1]. Kalbhen DA, et al. Nutmeg as a narcotic. A contribution to the chemistry and pharmacology of nutmeg (Myristica fragrans).Angew Chem Int Ed Engl. 1971 Jun;10(6):370-4. [2]. Dawidowicz AL, et al. Simple and rapid determination of myristicin in human serum.Forensic Toxicol. 2013 Jan;31(1):119-123. Epub 2012 Aug 15. Chemical & Physical Properties Density 1.1±0.1 g/cm3 Boiling Point 276.5±0.0 °C at 760 mmHg Melting Point <-20ºC Molecular Formula C11H12O3 Molecular Weight 192.211 Flash Point 89.8±16.0 °C Exact Mass 192.078644 PSA 27.69000 LogP 3.26 Appearance of Characters oil | clear, light yellow Vapour Pressure 0.0±0.5 mmHg at 25°C Index of Refraction 1.540 InChIKey BNWJOHGLIBDBOB-UHFFFAOYSA-N SMILES C=CCc1cc(OC)c2c(c1)OCO2 |
| Use of | Myristicine act as a serotonin receptor antagonist, a weak monamine oxidase (MAO) inhibitor. Myristicine is the main component of nutmeg essential oil from Myristica fragrans Houtt. Myristicine abuse produce hallucinogenic effects, organ damage, deliriumand others[1]. Properties Articles35 Name 4-methoxy-6-prop-2-enyl-1,3-benzodioxole Synonym More Synonyms Myristicin Biological Activity Description Myristicine act as a serotonin receptor antagonist, a weak monamine oxidase (MAO) inhibitor. Myristicine is the main component of nutmeg essential oil from Myristica fragrans Houtt. Myristicine abuse produce hallucinogenic effects, organ damage, deliriumand others[1]. Related Catalog Research Areas >> Neurological Disease Signaling Pathways >> GPCR/G Protein >> 5-HT Receptor Signaling Pathways >> Neuronal Signaling >> 5-HT Receptor References [1]. Kalbhen DA, et al. Nutmeg as a narcotic. A contribution to the chemistry and pharmacology of nutmeg (Myristica fragrans).Angew Chem Int Ed Engl. 1971 Jun;10(6):370-4. [2]. Dawidowicz AL, et al. Simple and rapid determination of myristicin in human serum.Forensic Toxicol. 2013 Jan;31(1):119-123. Epub 2012 Aug 15. Chemical & Physical Properties Molecular Formula C11H12O3 Exact Mass 192.078644 PSA 27.69000 Appearance of Characters oil | clear, light yellow Index of Refraction 1.540 InChIKey BNWJOHGLIBDBOB-UHFFFAOYSA-N |
| Tax Rebate | 13.0% |
| Supervision | None. MFN tariff: 6.5%. Ordinary tariff: 20.0% |
| Transport Info | Product name: Purity: 98.0% |
| MSDS Transport Info | Module 14. Shipping information 14.1 UN dangerous goods number European Land Transport Danger Regulations: 3082 International Maritime Danger Regulations: 3082 International Air Transport Danger Regulations: 3082 14.2 Names specified by the United Nations (UN) European land transport hazard regulations: ENVIRONMENTALLY HAZARDOUS SUBSTANCE, LIQUID, N.O.S. (6-allyl-4-methoxy-1,3- benzodioxole) IMDG: ENVIRONMENTALLY HAZARDOUS SUBSTANCE, LIQUID, N.O.S. (6-allyl-4-methoxy-1,3- benzodioxole) International air transport hazard regulations: Environmentally hazardous substance, liquid, n.o.s. (6-allyl-4-methoxy-1,3-benzodioxole) 14.3 Transport hazard categories European land transport Dangerous Regulations: 9 International sea transport Dangerous Regulations: 9 International air transport Dangerous Regulations: 9 14.4 Package group European Land Transport Danger Regulations: III International Maritime Transport Danger Regulations: III International Air Transport Danger Regulations: III 14.5 Environmental hazards European Land Transport Dangerous Regulations: Yes International Maritime Transport Dangerous Regulations Maritime Pollutants: Yes International Air Transport Dangerous Regulations: Yes 14.6 Special reminder to users further information Dangerous goods are individually packaged, with liquids exceeding 5 liters or solids exceeding 5 kilograms. The outer packaging of each independent package and the combined independent inner package must have EHS on it. Identification (according to European ADR Regulation 2.2.9.1.10, IMDG Regulation 2.10.3), |
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