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(-)-Dihydrocarvyl acetate
(-)-Dihydrocarvyl acetate
ChemFaces products have been cited in many studies from excellent and top scientific journals
Product Name (-)-Dihydrocarvyl acetate
Price: $30 / 20mg
CAS No.: 20777-49-5
Catalog No.: CFN70082
Molecular Formula: C12H20O2
Molecular Weight: 196.2 g/mol
Purity: >=98%
Type of Compound: Monoterpenoids
Physical Desc.: Oil
Source: The essential oil of Mentha spicata L. var. crispa Benth.
Solvent: Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, etc.
Download: COA    MSDS
Similar structural: Comparison
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Size /Price /Stock 10 mM * 100 uL in DMSO / Inquiry / In-stock
10 mM * 1 mL in DMSO / Inquiry / In-stock
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Biological Activity
Description: Reference standards.
(-)-Dihydrocarvyl acetate Description
Source: The essential oil of Mentha spicata L. var. crispa Benth.
Solvent: Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, etc.
Storage: Providing storage is as stated on the product vial and the vial is kept tightly sealed, the product can be stored for up to 24 months(2-8C).

Wherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20C. Generally, these will be useable for up to two weeks. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour.

Need more advice on solubility, usage and handling? Please email to: service@chemfaces.com

After receiving: The packaging of the product may have turned upside down during transportation, resulting in the natural compounds adhering to the neck or cap of the vial. take the vial out of its packaging and gently shake to let the compounds fall to the bottom of the vial. for liquid products, centrifuge at 200-500 RPM to gather the liquid at the bottom of the vial. try to avoid loss or contamination during handling.
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Recently, ChemFaces products have been cited in many studies from excellent and top scientific journals

Cell. 2018 Jan 11;172(1-2):249-261.e12.
doi: 10.1016/j.cell.2017.12.019.
IF=36.216(2019)

PMID: 29328914

Cell Metab. 2020 Mar 3;31(3):534-548.e5.
doi: 10.1016/j.cmet.2020.01.002.
IF=22.415(2019)

PMID: 32004475

Mol Cell. 2017 Nov 16;68(4):673-685.e6.
doi: 10.1016/j.molcel.2017.10.022.
IF=14.548(2019)

PMID: 29149595

ACS Nano. 2018 Apr 24;12(4): 3385-3396.
doi: 10.1021/acsnano.7b08969.
IF=13.903(2019)

PMID: 29553709

Nature Plants. 2016 Dec 22;3: 16206.
doi: 10.1038/nplants.2016.205.
IF=13.297(2019)

PMID: 28005066

Sci Adv. 2018 Oct 24;4(10): eaat6994.
doi: 10.1126/sciadv.aat6994.
IF=12.804(2019)

PMID: 30417089
Calculate Dilution Ratios(Only for Reference)
1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 5.0968 mL 25.4842 mL 50.9684 mL 101.9368 mL 127.421 mL
5 mM 1.0194 mL 5.0968 mL 10.1937 mL 20.3874 mL 25.4842 mL
10 mM 0.5097 mL 2.5484 mL 5.0968 mL 10.1937 mL 12.7421 mL
50 mM 0.1019 mL 0.5097 mL 1.0194 mL 2.0387 mL 2.5484 mL
100 mM 0.051 mL 0.2548 mL 0.5097 mL 1.0194 mL 1.2742 mL
* Note: If you are in the process of experiment, it's need to make the dilution ratios of the samples. The dilution data of the sheet for your reference. Normally, it's can get a better solubility within lower of Concentrations.
Protocol
Structure Identification:
Nippon Nōgeikagaku Kaishi, 1976,50(6):287-289.
Essential Oil of Mentha spicata L. var. crispa Benth. Grown in Winter Season.[Reference: WebLink]
The constituents of the essential oil of Mentha spicata L. var. crispa Benth. grown in the winter season were investigated.
METHODS AND RESULTS:
The major components in the oil were detected as (-)-carvone (1), (+)-dihydrocarvone (2), (-)-dihydrocarveol (3), (-)-Dihydrocarvyl acetate (4), (+)-neodihydrocarveol (5) and (-)-cis-carvyl acetate (8). The content of above oxygenated compounds from each oil col-lected in November, December, January and Febrary was showed as follows; 1 (59.1, 40.1, 16.2 and 8.0%), 2 (3.3, 5.8, 3.1 and 3.5%), 3 (6.1, 10.1, 15.7 and 7.8%), 4 (3.8, 10.8, 26.0 and 30.1 %), 5 (5.1, 16.5, 17.4 and 18.5%) and 8 (4.1, 6.4, 9.4 and 14.7%).
CONCLUSIONS:
On the basis of seasonal variation of these components in this species, the following biosynthetic pathways in vivo were postulated: carvone (1) is reduced to afford dihydrocarvone (2). As a next step, 2 thus produced yields dihydrocarveol (3) and neodihydrocarveol (5). The former is further con-verted to its acetate (4) by esterification. While 1 is also converted into cis-carvyl acetate (8) via its alcohol, and a part of 8 proceeds to 4.
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