CAS 6485-40-1

(-)-Carvone

Description:

(-)-Carvone is a naturally occurring organic compound classified as a monoterpenoid ketone, primarily recognized for its distinct minty aroma, which is reminiscent of spearmint. It is a chiral molecule, existing in two enantiomeric forms, with the (-)-enantiomer being the one commonly found in nature. The compound has a molecular formula of C10H14O and features a characteristic carbonyl group (C=O) within its structure, contributing to its reactivity and fragrance properties. (-)-Carvone is soluble in organic solvents and exhibits limited solubility in water. It is widely used in the food and fragrance industries as a flavoring agent and scent component. Additionally, (-)-Carvone has been studied for its potential biological activities, including antimicrobial and anti-inflammatory properties. Its presence in essential oils, particularly from caraway and spearmint, highlights its significance in both culinary and therapeutic applications. As a compound, it is generally regarded as safe for consumption, although individual sensitivities may vary.

Formula: C₁₀H₁₄O

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

InChI key: InChIKey=ULDHMXUKGWMISQ-SECBINFHSA-N

SMILES: C(C)(=C)[C@H]1CC(=O)C(C)=CC1

Synonyms:

• (-)-(5R)-Carvone
• (-)-(R)-Carvone
• (-)-Carvone
• (-)-p-Mentha-6,8-dien-2-one
• (4R)-(-)-Carvone
• (5R)-2-Methyl-5-(1-methylethenyl)-2-cyclohexen-1-one
• (5R)-2-Methyl-5-(prop-1-en-2-yl)cyclohex-2-en-1-one
• (5R)-2-hydroxy-5-isopropenyl-cyclohex-2-en-1-one
• (5S)-2-methyl-5-(prop-1-en-2-yl)cyclohex-2-en-1-one
• (R)-(-)-p-Mentha-6,8-dien-2-one
• (R)-2-Methyl-5-(1-methylethenyl)-2-cyclohexen-1-one
• 1,1-Methyl-4-Isopropenyl-6-Cyclohexen-2-One-, (5R)
• 2-Cyclohexen-1-one, 2-methyl-5-(1-methylethenyl)-, (5R)-
• 2-Cyclohexen-1-one, 2-methyl-5-(1-methylethenyl)-, (R)-
• <span class="text-smallcaps">L</span>-(-)-Carvone
• Cyclohex-2-En-1-One, 2-Methyl-5- (1-Methylethenyl)-, (R)- (-)-
• L-1-Methyl-4-Isopropenyl-6-Cyclohexen-2-One
• L-1-methyl-4-isopropenyl-6-cyclohexene-2-one
• L-Carvon
• L-P-Menta-1(6),8-Dien-2-Ona
• L-P-Mentha-1(6),8-Diene-2-One
• l-p-Mentha-1(6),8-dien-2-on
• l-p-Mentha-1(6),8-dien-2-one
• p-Mentha-6,8-dien-2-one, (R)-(-)-
• L-CARVONE
• 6,8-p-menthadien-2-one
• (R)-5-ISOPROPENYL-2-METHYL-2-CYCLOHEXENONE
• LAEVO-CARVEONE
• 1'CARVONE
• P-MENTHA-6,8-DIENE-2-ONE
• 1-Methyl-4-isopropenyl-6-cyclohexen-2-one
• FEMA 2249
• CARVOL
• L-P-MENTHA-6,8-DIEN-2-ONE
• (R)-(-)-5-ISOPROPHENYL-2-METHYL-2-CYCLOHEXENONE
• 4-MENTHA-6,8-DIEN-2ONE

(R)-(-)-Carvone

CAS: 6485-40-1

Formula: C₁₀H₁₄O

Purity: >99.0%(GC)

Color and Shape: Colorless to Light yellow to Light orange clear liquid

Molecular weight: 150.22

Ref: 3B-C0703

(R)-(-)-Carvone, 98%

CAS: 6485-40-1

(R)-(-)-Carvone is used in the flavor and food industry such as chewing gum additives. It is used in air freshening products such as in essential oils as well as in aromatherapy and alternative medicine. It is used to prepare carvomenthol, carvomenthone, dihydrocarvone, carveol and limonene. It re

Formula: C₁₀H₁₄O

Purity: 98%

Color and Shape: Clear colorless to yellow, Liquid

Molecular weight: 150.22

Ref: 02-A13900

(-)-Carvone

CAS: 6485-40-1

(-)-Carvone analytical standard provided with w/w absolute assay, to be used for quantitative titration.

Formula: C₁₀H₁₄O

Purity: (GC) ≥99% (sum of enantiomers)

Color and Shape: Liquid

Molecular weight: 150.22

Ref: 11-5012S

2-Cyclohexen-1-one, 2-methyl-5-(1-methylethenyl)-, (5R)-

CAS: 6485-40-1

Formula: C₁₀H₁₄O

Purity: 99%

Color and Shape: Liquid

Molecular weight: 150.2176

Ref: IN-DA00IBF0

L-(-)-Carvone

CAS: 6485-40-1

L-(-)-Carvone

Purity: 99%

Molecular weight: 150.22g/mol

Ref: 54-OR1013617

(-)-Carvone

CAS: 6485-40-1

(-)-Carvone

Purity: ≥95%

Molecular weight: 150.22g/mol

Ref: 54-BUP18973

(R)-(-)-Carvone

CAS: 6485-40-1

Formula: C₁₀H₁₄O

Purity: ≥ 99.0%

Color and Shape: Colourless to light-yellow liquid

Molecular weight: 150.22

Ref: 7W-GL3381

R-(-)-Carvone-4,4,6,6-d499 atom % D

CAS: 6485-40-1

Purity: 99 atom % D

Molecular weight: 154.24

Ref: 3U-D8034

L-Carvone

CAS: 6485-40-1

Formula: C₁₀H₁₄O

Color and Shape: Neat

Molecular weight: 150.22

Ref: 04-CA11052020

(R)-(-)-Carvone

CAS: 6485-40-1

Formula: C₁₀H₁₄O

Molecular weight: 150.22

Ref: 4Z-C-259002

(-)-Carvone

CAS: 6485-40-1

(-)-Carvone is a natural product which probably has antioxidant and anti-inflammatory capabilities.

Formula: C₁₀H₁₄O

Purity: 97.21%

Color and Shape: Pale-Yellowish Or Colorless Liquid Liquid

Molecular weight: 150.22

Ref: TM-TN1468

(-)-carvone

CAS: 6485-40-1

Alicyclic ketone

Formula: C₁₀H₁₄O

Purity: ≥ 95.0 % (GC)

Color and Shape: Liquid

Molecular weight: 150.22

Ref: 5G-80099

(R)-(-)-Carvone 4,4,6,6-d4

Controlled Product

CAS: 6485-40-1

Applications (R)-(-)-Carvone-d4 is an intermediate in synthesizing (+)-Limonene-d5 (L461742). It is present in blood oranges which show inhibition of angiogenesis in human colon cancer cells. Extracted from the oils of Mentha spicata it shows antimicrobial activity.
References Chidambara Murthy, K. et al.: Life Sci.,91, 429 (2012); Aggarwal, K. et al.: Flav. Frag. J., 17, 59 (2002)

Formula: C₁₀D₄H₁₀O

Color and Shape: Neat

Molecular weight: 154.242

Ref: TR-C184697

(R)-(-)-Carvone

CAS: 6485-40-1

Applications (R)-(-)-Carvone, is an antinociceptive monoterpene found as the main active constituent of essential oils obtained from plants of the genus Mentha. It is a novel agonist of TRPV1 channels. It can also be used as a chiral starting material.
References Goncalves, J.C., et al.: Cytometry part A., 83(2), 212 (2013); Liebigs ann., Chem., 403 (1993);

Formula: C₁₀H₁₄O

Color and Shape: Colourless

Molecular weight: 150.22

Ref: TR-C184695

(R)-2-Methyl-5-(prop-1-en-2-yl)cyclohex-2-enone

CAS: 6485-40-1

Formula: C₁₀H₁₄O

Purity: 95%

Color and Shape: Liquid, Clear

Molecular weight: 150.221

Ref: 10-F240922

(R)-2-Methyl-5-(prop-1-en-2-yl)cyclohex-2-enone

CAS: 6485-40-1

(R)-2-Methyl-5-(prop-1-en-2-yl)cyclohex-2-enone is an organic compound that has been shown to induce apoptosis in prostate cancer cells. The mechanism of this induction is not yet fully understood, but it may be due to the inhibition of the synthesis of proteins required for cell division. It also had a significant effect on locomotor activity in mice. This compound has been shown to have acute toxicities, and its phase transition temperature is below room temperature. It can be used as a fumigant and an inorganic acid, and it has been proposed as a potential fluorescence probe for natural compounds.

Purity: Min. 95%

Ref: 3D-FM142896