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Art. -Nr.: HY-126027

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(+)-3-Carene

(+)-3-Carene is the (+)-enantiomer of 3-Carene (HY-N6663). (+)-3-Carene is a conifer metabolite associated with insect resistance in conifers. (+)-3-Carene can be used in studies related to pest control.

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CAS. Nr.: 498-15-7
Formel: C₁₀H₁₆
Molecular Weight:136.23

Speicherung:

RT, stored under nitrogen.

In solvent -80°C, 2 years , -20°C, 1 year

Data Sheet (268 KB)

(+)-3-Carene Chemical Structure

CAS. Nr.: 498-15-7

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Biologische Aktivität

Beschreibung

In Vitro

(+)-3-Carene serves as an intermediate to react and form α-3,4-epoxycarene, β-3,4-epoxycarene and other compounds^[1].
(+)-3-Carene exhibits significantly higher basal accumulation in the top stem tissues of resistant Picea abies clone H898 relative to susceptible clones; methyl jasmonate treatment only triggers a slight yet notable elevation of this compound in susceptible Picea sitchensis clone Q903, whereas its level stays unaltered and persistently higher in resistant clone H898^[2].
(+)-3-Carene is produced with similar catalytic efficiency by recombinant PsTPS-3car1 enzymes from both resistant and sensitive Picea sitchensis trees, while PsTPS-3car2 (R) from resistant plants shows lower catalytic efficiency, and PsTPS-3car3 (S) from sensitive plants exhibits negligible catalytic activity^[2].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

Chemical Information

CAS. Nr. 498-15-7
Appearance Liquid
Molecular Weight 136.23
Formel C₁₀H₁₆
Color Colorless to off-white
SMILES

CC1=CC[C@H]2C(C)([C@H]2C1)C
Structure Classification
- Terpenoids
- Other Monoterpenes
Initial Source
Versand

Room temperature in continental US; may vary elsewhere.

Speicherung

RT, stored under nitrogen

In solvent	-80°C	2 years
	-20°C	1 year

Reinheit & Dokumentation

Select Batch:

Reinheit: 99.98%

Assay: 99.98%

ee.: 99.98%

Data Sheet (268 KB)
SDS (252 KB)
- Français - FR (252 KB)
- Deutsch - DE (252 KB)
- Norwegian - NO (252 KB)
- Español - ES (252 KB)
- Swedish - SV (252 KB)
- Italian - IT (252 KB)
- Korean - KR (252 KB)
- Portuguese - PT (252 KB)
COA (2659 KB)
Elemental Analysis Report (2659 KB)
HNMR (2659 KB)
CNMR (2659 KB)
RP-HPLC (2659 KB)
NP-HPLC (2659 KB)
MS (2659 KB)
LCMS (2659 KB)
IR (2659 KB)
GC (2659 KB)
OR (2659 KB)
SDS-PAGE (2659 KB)
SEC-HPLC (2659 KB)
Other Report (2659 KB)
Handling Instructions (2659 KB)

Verweise

[1]. Curlat S. Recent Studies of (+)-3-Carene Transformations with the Retention of the Native Framework. Chemistry Journal of Moldova. General, Industrial and Ecological Chemistry, 2019, 14(2): 32-55.

[2]. Hall DE, et al. An integrated genomic, proteomic and biochemical analysis of (+)-3-carene biosynthesis in Sitka spruce (Picea sitchensis) genotypes that are resistant or susceptible to white pine weevil. The Plant journal : for cell and molecular biology. 2011 Mar;65(6):936-48. [Content Brief]

[3]. Ji X. Synthesis of (3,3-dimethylcyclopropane-1,2-diyl) dimethanol from 3-carene. Journal of Chemical Research, 2025.

Calculators

Molaritätsrechner

Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

Mass Mass

Konzentration Konzentration

Volumen Volumen

Molecular Weight Molecular Weight

Verdünnungsrechner

Konzentration _{(Stammlösung)} × Volumen _{(Stammlösung)} = Konzentration _{(Ziellösung)} × Volumen _{(Ziellösung)}

Konzentration _{(Stammlösung)} Konzentration _{(Stammlösung)}

Volumen _{(Stammlösung)} Volumen _{(Stammlösung)}

Konzentration _{(Ziellösung)} Konzentration _{(Ziellösung)}

Volumen _{(Ziellösung)} Volumen _{(Ziellösung)}

Help & FAQs

How should lyophilized recombinant proteins be reconstituted and stored?

1. Before opening the cap, centrifuge the vial at 13000 rpm for 20-30 seconds. This step will ensure that any lyophilized powder that may have adhered to the cap or walls is collected at the bottom of the vial, minimizing the risk of product loss.

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(+)-3-Carene

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(R)-3-Hydroxybutanoic acid

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(R)-D2PM

Hydroquinidine

(S)-1-Boc-3-methylpiperazine

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(+)-3-Carene

L-Lactic acid sodium

(-)-Isopulegol

(R)-(-)-α-Phellandrene

(R)-3-Hydroxybutanoic acid

3-Carene

(R)-D2PM

Hydroquinidine

(S)-1-Boc-3-methylpiperazine

Biologische Aktivität

Chemical Information

Reinheit & Dokumentation

Verweise

Calculators

Help & FAQs

(+)-3-Carene Related Classifications

HY-126027 Related Classifications