(S)-(-)-Limonene

CAS# 5989-54-8

(S)-(-)-Limonene

Catalog No. BCN9766----Order now to get a substantial discount!

Product Name & Size Price Stock
(S)-(-)-Limonene: 5mg $12 In Stock
(S)-(-)-Limonene: 10mg Please Inquire In Stock
(S)-(-)-Limonene: 20mg Please Inquire Please Inquire
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(S)-(-)-Limonene: 500mg Please Inquire Please Inquire
(S)-(-)-Limonene: 1000mg Please Inquire Please Inquire
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Chemical structure

(S)-(-)-Limonene

3D structure

Chemical Properties of (S)-(-)-Limonene

Cas No. 5989-54-8 SDF Download SDF
PubChem ID 439250 Appearance Oil
Formula C10H16 M.Wt 136.2
Type of Compound Monoterpenoids Storage Desiccate at -20°C
Solubility Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
Chemical Name (4S)-1-methyl-4-prop-1-en-2-ylcyclohexene
SMILES CC1=CCC(CC1)C(=C)C
Standard InChIKey XMGQYMWWDOXHJM-SNVBAGLBSA-N
Standard InChI InChI=1S/C10H16/c1-8(2)10-6-4-9(3)5-7-10/h4,10H,1,5-7H2,2-3H3/t10-/m1/s1
General tips For obtaining a higher solubility , please warm the tube at 37 ℃ and shake it in the ultrasonic bath for a while.Stock solution can be stored below -20℃ for several months.
We recommend that you prepare and use the solution on the same day. However, if the test schedule requires, the stock solutions can be prepared in advance, and the stock solution must be sealed and stored below -20℃. In general, the stock solution can be kept for several months.
Before use, we recommend that you leave the vial at room temperature for at least an hour before opening it.
About Packaging 1. The packaging of the product may be reversed during transportation, cause the high purity compounds to adhere to the neck or cap of the vial.Take the vail out of its packaging and shake gently until the compounds fall to the bottom of the vial.
2. For liquid products, please centrifuge at 500xg to gather the liquid to the bottom of the vial.
3. Try to avoid loss or contamination during the experiment.
Shipping Condition Packaging according to customer requirements(5mg, 10mg, 20mg and more). Ship via FedEx, DHL, UPS, EMS or other couriers with RT, or blue ice upon request.

(S)-(-)-Limonene Dilution Calculator

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(S)-(-)-Limonene Molarity Calculator

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Preparing Stock Solutions of (S)-(-)-Limonene

1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 7.3421 mL 36.7107 mL 73.4214 mL 146.8429 mL 183.5536 mL
5 mM 1.4684 mL 7.3421 mL 14.6843 mL 29.3686 mL 36.7107 mL
10 mM 0.7342 mL 3.6711 mL 7.3421 mL 14.6843 mL 18.3554 mL
50 mM 0.1468 mL 0.7342 mL 1.4684 mL 2.9369 mL 3.6711 mL
100 mM 0.0734 mL 0.3671 mL 0.7342 mL 1.4684 mL 1.8355 mL
* Note: If you are in the process of experiment, it's necessary to make the dilution ratios of the samples. The dilution data above is only for reference. Normally, it's can get a better solubility within lower of Concentrations.

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References on (S)-(-)-Limonene

Transforming yeast peroxisomes into microfactories for the efficient production of high-value isoprenoids.[Pubmed:33268495]

Proc Natl Acad Sci U S A. 2020 Dec 2. pii: 2013968117.

Current approaches for the production of high-value compounds in microorganisms mostly use the cytosol as a general reaction vessel. However, competing pathways and metabolic cross-talk frequently prevent efficient synthesis of target compounds in the cytosol. Eukaryotic cells control the complexity of their metabolism by harnessing organelles to insulate biochemical pathways. Inspired by this concept, herein we transform yeast peroxisomes into microfactories for geranyl diphosphate-derived compounds, focusing on monoterpenoids, monoterpene indole alkaloids, and cannabinoids. We introduce a complete mevalonate pathway in the peroxisome to convert acetyl-CoA to several commercially important monoterpenes and achieve up to 125-fold increase over cytosolic production. Furthermore, peroxisomal production improves subsequent decoration by cytochrome P450s, supporting efficient conversion of (S)-(-)-Limonene to the menthol precursor trans-isopiperitenol. We also establish synthesis of 8-hydroxygeraniol, the precursor of monoterpene indole alkaloids, and cannabigerolic acid, the cannabinoid precursor. Our findings establish peroxisomal engineering as an efficient strategy for the production of isoprenoids.

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