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22070

Supelco

(+)-Carvon

analytical standard

Synonym(e):

(+)-p-Mentha-6,8-dien-2-on, (S)-5-Isopropenyl-2-methyl-2-cyclohexenon

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About This Item

Empirische Formel (Hill-System):
C10H14O
CAS-Nummer:
2244-16-8
Molekulargewicht:
150.22
Beilstein:
2042970
EG-Nummer:
218-827-2
MDL-Nummer:
MFCD00062997
UNSPSC-Code:
85151701
PubChem Substanz-ID:
329752243
NACRES:
NA.24

Qualität

analytical standard

Qualitätsniveau

100

Assay

≥98.5% (sum of enantiomers, GC)

Optische Aktivität

[α]20/D +61±2°, neat

Haltbarkeit

limited shelf life, expiry date on the label

Methode(n)

HPLC: suitable
gas chromatography (GC): suitable

Brechungsindex

n20/D 1.499

bp

228-230 °C (lit.)

Dichte

0.960 g/mL at 20 °C (lit.)

Anwendung(en)

agriculture
environmental
food and beverages

Format

neat

SMILES String

CC(=C)[C@H]1CC=C(C)C(=O)C1

InChI

1S/C10H14O/c1-7(2)9-5-4-8(3)10(11)6-9/h4,9H,1,5-6H2,2-3H3/t9-/m0/s1

InChIKey

ULDHMXUKGWMISQ-VIFPVBQESA-N

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Allgemeine Beschreibung

(+)-Carvone (S-carvone), is a monoterpene which has the ability to affect regulation of plant growth and development and microbial activity, it can also prevent sprouting in potato, through inhibition of the induction of phenylalanine ammonia-lyase (PAL) activity, thereby blocking suberisation.

Anwendung

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Sonstige Hinweise

This compound is commonly found in plants of the genus: carum mentha zingiber

Piktogramme

Exclamation mark
GHS07

Signalwort

Warning

H-Sätze

H317

Gefahreneinstufungen

Skin Sens. 1A

Lagerklassenschlüssel

10 - Combustible liquids

WGK

WGK 1

Flammpunkt (°F)

204.1 °F - closed cup

Flammpunkt (°C)

95.6 °C - closed cup

Persönliche Schutzausrüstung

Eyeshields, Gloves

Choose from one of the most recent versions:

Analysenzertifikate (COA)

Lot/Batch Number
BCCG0400
BCCC7860
BCCC4533
BCBZ8472
BCBZ3308

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L-Carvon ≥97%, FCC, FG

Sigma-Aldrich

W224901

L-Carvon

(R)-(+)-Limone analytical standard

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62118

(R)-(+)-Limone

Piperiton analytical standard

Supelco

79899

Piperiton

(1R)-(−)-Menthyl-acetat analytical standard

Supelco

45985

(1R)-(−)-Menthyl-acetat

Eucalyptol analytical standard

Supelco

29210

Eucalyptol

(S)-(−)-Limonen analytical standard

Supelco

62128

(S)-(−)-Limonen

Bisabololoxid A primary reference standard

00630590

Bisabololoxid A

Possible regulatory role of phenylalanine ammonia?lyase in the production of anthocyanins in asparagus (Asparagus officinalis L).
Flores, Francisco B., et al.
Journal of the Science of Food and Agriculture, 85.6, 925-930 (2005)
Raul Conde et al.
Phytomedicine : international journal of phytotherapy and phytopharmacology, 18(14), 1197-1201 (2011-08-02)
There is no universally accepted and effective prophylaxis of migraine headache episodes. Thus we aimed to investigate the effects of Lippia alba (Mill.) N. E. Brown, an herb with many effects on central nervous system, on pain frequency and intensity
Marta Goretti et al.
Bioresource technology, 121, 290-297 (2012-08-04)
Response surface methodology was applied in optimizing the asymmetric bioreduction of (4S)-(+)-carvone to dihydrocarvone (with low incidence of unsought side reactions) by using whole-cells of Cryptococcus gastricus. A factorial design (2(5)) including five independent variables was performed: X(1)=incubation time; X(2)=pH;
Philipp Klahn et al.
Organic letters, 14(5), 1250-1253 (2012-02-14)
The total synthesis of (+)-cyperolone, an eudesmane-derived sesquiterpenoid from Cyperus rotundus, is described. The de novo synthesis was accomplished via a 15 step sequence starting from (R)-(-)-carvone. The synthetic route features a platinum-catalyzed cycloisomerization to rapidly construct the bicyclic core
Elissavet E Anagnostaki et al.
Organic letters, 15(1), 152-155 (2012-12-22)
The synthesis of hydroxyelemane 5 from (R)-carvone and its utilization as a common synthetic scaffold to produce structurally diverse germacrane and guaiane sesquiterpenes are described. A highly enantio- and stereoselective biomimetic tandem oxy-Cope/ene rearrangement was used as the key reaction
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Artikel

Chiral GC Analysis of Carvone Enantiomers in Essential Oils

In this study we demonstrate the separation of D- and L-carvone enantiomers in samples of caraway seed, dill seed, native spearmint and scotch spearmint essential oils using an Astec CHIRALDEX G-TA capillary GC column.

Unser Team von Wissenschaftlern verfügt über Erfahrung in allen Forschungsbereichen einschließlich Life Science, Materialwissenschaften, chemischer Synthese, Chromatographie, Analytik und vielen mehr..

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