CAS 6485-40-1

(-)-Carvona

Descrição:

(-)-Carvona é um composto orgânico que ocorre naturalmente, classificado como uma cetona monoterpenoide, reconhecido principalmente por seu distinto aroma de menta, que lembra a hortelã. É uma molécula quiral, existindo em duas formas enantioméricas, sendo o enantiômero (-) aquele comumente encontrado na natureza. O composto tem uma fórmula molecular de C10H14O e apresenta um grupo carbonila característico (C=O) dentro de sua estrutura, contribuindo para sua reatividade e propriedades de fragrância. (-)-Carvona é solúvel em solventes orgânicos e exibe solubilidade limitada em água. É amplamente utilizado nas indústrias alimentícia e de fragrâncias como agente aromatizante e componente de cheiro. Além disso, (-)-Carvona tem sido estudado por suas potenciais atividades biológicas, incluindo propriedades antimicrobianas e anti-inflamatórias. Sua presença em óleos essenciais, particularmente de cominho e hortelã, destaca sua importância tanto em aplicações culinárias quanto terapêuticas. Como composto, geralmente é considerado seguro para consumo, embora as sensibilidades individuais possam variar.

Fórmula: 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

Chave InChI: InChIKey=ULDHMXUKGWMISQ-SECBINFHSA-N

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

Sinónimos:

• (-)-(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

Fórmula: C₁₀H₁₄O

Pureza: >99.0%(GC)

Cor e Forma: Colorless to Light yellow to Light orange clear liquid

Peso molecular: 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

Fórmula: C₁₀H₁₄O

Pureza: 98%

Cor e Forma: Clear colorless to yellow, Liquid

Peso molecular: 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.

Fórmula: C₁₀H₁₄O

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

Cor e Forma: Liquid

Peso molecular: 150.22

Ref: 11-5012S

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

CAS: 6485-40-1

Fórmula: C₁₀H₁₄O

Pureza: 99%

Cor e Forma: Liquid

Peso molecular: 150.2176

Ref: IN-DA00IBF0

L-(-)-Carvone

CAS: 6485-40-1

L-(-)-Carvone

Pureza: 99%

Peso molecular: 150.22g/mol

Ref: 54-OR1013617

(-)-Carvone, 10mM (in DMSO)

CAS: 6485-40-1

(-)-Carvone, 10mM (in DMSO)

Pureza: ≥95%

Peso molecular: 150.22g/mol

Ref: 54-BUP18973

(R)-(-)-Carvone

CAS: 6485-40-1

Fórmula: C₁₀H₁₄O

Pureza: ≥ 99.0%

Cor e Forma: Colourless to light-yellow liquid

Peso molecular: 150.22

Ref: 7W-GL3381

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

CAS: 6485-40-1

Pureza: 99 atom % D

Peso molecular: 154.24

Ref: 3U-D8034

L-Carvone

CAS: 6485-40-1

Fórmula: C₁₀H₁₄O

Cor e Forma: Neat

Peso molecular: 150.22

Ref: 04-CA11052020

(R)-(-)-Carvone

CAS: 6485-40-1

Fórmula: C₁₀H₁₄O

Peso molecular: 150.22

Ref: 4Z-C-259002

(-)-Carvone

CAS: 6485-40-1

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

Fórmula: C₁₀H₁₄O

Pureza: 97.21%

Cor e Forma: Pale-Yellowish Or Colorless Liquid Liquid

Peso molecular: 150.22

Ref: TM-TN1468

(-)-carvone

CAS: 6485-40-1

Alicyclic ketone

Fórmula: C₁₀H₁₄O

Pureza: ≥ 95.0 % (GC)

Cor e Forma: Liquid

Peso molecular: 150.22

Ref: 5G-80099

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

Produto Controlado

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)

Fórmula: C₁₀D₄H₁₀O

Cor e Forma: Neat

Peso molecular: 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);

Fórmula: C₁₀H₁₄O

Cor e Forma: Colourless

Peso molecular: 150.22

Ref: TR-C184695

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

CAS: 6485-40-1

Fórmula: C₁₀H₁₄O

Pureza: 95%

Cor e Forma: Liquid, Clear

Peso molecular: 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.

Pureza: Min. 95%

Ref: 3D-FM142896