Then, use absorbent paper to pick up all liquid spill material. Service Tel: +86-571-87759741, Marketing Tel: +86-571-89739798 skype, Copyright©2010-2020 Guidechem 浙B2-20090288-37. Lewis, K.A., Tzilivakis, J., Warner, D. and Green, A. Specific Gravity: 0.965 at 68 ° F (NTP, 1992) Boiling Point: 446 ° F at 760 mm Hg (NTP, 1992) Molecular Weight: 150.22 (NTP, 1992) Water Solubility: less than 1 mg/mL at 77° F (NTP, 1992) Ionization Potential: data unavailable. Cyclohexanone,2-methyl-5-(1-methylethenyl)-, Cyclohexanone,2-methyl-5-(1-methylethenyl)-, (2R,5R)-rel-, (1alpha,4alpha,6alpha)-(+)-1-methyl-4-(1-methylvinyl)-7-oxabicyclo[4.1.0]heptan-2-one, 2-Cyclohexen-1-one,5-(1-hydroxy-1-methylethyl)-2-methyl-, (5S)-, 2-Cyclohexen-1-one,5-(1-hydroxy-1-methylethyl)-2-methyl-, 2-Cyclohexen-1-one,2-methyl-5-(1-methylethenyl)-, oxime, 7-Oxabicyclo[4.1.0]heptan-2-one,1-methyl-4-(1-methylethenyl)-, (1S,4R,6S)-, 7-Oxabicyclo[4.1.0]heptan-2-one,1-methyl-4-(1-methylethenyl)-, Cyclohexanone, 2-methyl-5-(1-methylethenyl)-, (2R,5S)-. (NTP, 1992). ( $-$ )-Carvone, its enantiomer, is the main component of spearmint oil and gives it its characteristic odor. May be sensitive to prolonged exposure to light and air. This chemical is combustible. D-Carvone is a monoterpene ketone that can be used as a flavoring agent. EYES: First check the victim for contact lenses and remove if present. Carvone: EINECS: 202-759-5 CAS No. molecule looks like, and the melting point to identity between isomers, the unknown molecules were classified. SMALL SPILLS AND LEAKAGE: If you spill this chemical, FIRST REMOVE ALL SOURCES OF IGNITION. Xiamen Zhongyuan Hongye Chemical Co., Ltd. Carvone is a member of a family of chemicals called terpenoids. Packaging 1 kg in poly bottle 100 g in poly bottle 5 kg in poly drum Other Notes Download our Flavors and Fragrances Catalog to view our entire product line. (NTP, 1992). It occurs naturally in essential oil of caraway seeds and citrus fruits. MINIMUM PROTECTIVE CLOTHING: If Tyvek-type disposable protective clothing is not worn during handling of this chemical, wear disposable Tyvek-type sleeves taped to your gloves. 【Melting Point】 25.2 【Boiling Point】 227 【Vapor Pressure】 0.07 (25 C) 【Density】 0.9652 g/cm3 (15 C) 【Partition Coefficient】 2.27 【Heat Of Vaporization】 46.7 kJ/mol 【Usage】 Used in the food, flavoing and air freshening products.3. IMMEDIATELY transport the victim after flushing eyes to a hospital even if no symptoms (such as redness or irritation) develop. listed below. Guidechem provides L(-)-Carvone chemical database query, including CAS registy number 6485-40-1, L(-)-Carvone MSDS (Material Safety Data Sheet), nature, English name, manufacturer, function/use, molecular weight, density, boiling point, melting point, structural formula, etc. Flush victim's eyes with water or normal saline solution for 20 to 30 minutes while simultaneously calling a hospital or poison control center. (NTP, 1992). A = EU regulatory and evaluation data as published by EC, EFSA (RAR, DAR & Conclusion dossiers), EMA (e.g. EU Annex III PIC DGD) (, A = Chromosome aberration (EFSA database), E = Unspecified genotoxicity type (miscellaneous data source), (Also known as: p-mentha-6,8-dien-2-one; carvone; spearment oil component; carvone), A fungicide and plant growth regulator often used as a potato sprouting inhibitor, Authorised for use and widely used for over 10 years, EC Regulation 1107/2009 (repealing 91/414), Approved for use (✓) or known to be used (#) in the following EU-27 Member States, Known to be used in the following countries, International Chemical Identifier key (InChIKey), International Chemical Identifier (InChI), InChI=1S/C10H14O/c1-7(2)9-5-4-8(3)10(11)6-9/h4,9H,1,5-6H2,2-3H3/t9-/m1/s1, Cambridge Crystallographic Data Centre diagrams, Carvone is found naturally in many essential oils including spearmint (, 5-isopropenyl-2-methylcyclohex-2-en-1-one, 2-Methyl-5-(1-methylvinyl)cyclohex-2-en-1-one, Relevant Environmental Water Quality Standards, Herbicide Resistance Classification (HRAC), Herbicide Resistance Classification (WSSA), Insecticide Resistance Classification (IRAC), Fungicide Resistance Classification (FRAC), Usually supplied in formulations for hot or cold fogging for indoor use only, Source; quality score; and other information, Solubility - In organic solvents at 20 °C (mg l⁻¹), Octanol-water partition coefficient at pH 7, 20 °C, Henry's law constant at 25 °C (Pa m³ mol⁻¹), Dissipation rate RL₅₀ on and in plant matrix, Aqueous hydrolysis DT₅₀ (days) at 20 °C and pH 7, Aquatic invertebrates - Acute 48 hour EC₅₀ (mg l⁻¹), Aquatic invertebrates - Chronic 21 day NOEC (mg l⁻¹), Aquatic crustaceans - Acute 96 hour LC₅₀ (mg l⁻¹), Sediment dwelling organisms - Acute 96 hour LC₅₀ (mg l⁻¹), Sediment dwelling organisms - Chronic 28 day NOEC, static, water (mg l⁻¹), Sediment dwelling organisms - Chronic 28 day NOEC, sediment (mg kg⁻¹), Aquatic plants - Acute 7 day EC₅₀, biomass (mg l⁻¹), Algae - Acute 72 hour EC₅₀, growth (mg l⁻¹), Algae - Chronic 96 hour NOEC, growth (mg l⁻¹), Contact acute LD₅₀ (worst case from 24, 48 and 72 hour values - μg bee⁻¹), Oral acute LD₅₀ (worst case from 24, 48 and 72 hour values - μg bee⁻¹), Unknown mode acute LD₅₀ (worst case from 24, 48 and 72 hour values - μg bee⁻¹), Acute LD₅₀ (worst case from 24, 48 and 72 hour values - μg insect⁻¹), Earthworms - Chronic NOEC, reproduction (mg kg⁻¹), Threshold of Toxicological Concern (Cramer Class), Mammals - Dermal LD₅₀ (mg kg⁻¹ body weight), ADI - Acceptable Daily Intake (mg kg⁻¹ bw day⁻¹), ARfD - Acute Reference Dose (mg kg⁻¹ bw day⁻¹), AAOEL - Acute Acceptable Operator Exposure Level (mg kg⁻¹ bw day⁻¹), AOEL - Acceptable Operator Exposure Level - Systemic (mg kg⁻¹ bw day⁻¹), May cause gastrointestinal tract irritation with nausea, vomiting and diarrhea.