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7-Methoxy-1-tetralone
7-Methoxy-1-tetralone
ChemFaces products have been cited in many studies from excellent and top scientific journals
Product Name 7-Methoxy-1-tetralone
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CAS No.: 6836-19-7
Catalog No.: CFN90085
Molecular Formula: C11H12O2
Molecular Weight: 176.21 g/mol
Purity: >=98%
Type of Compound: Miscellaneous
Physical Desc.: Cryst.
Source: The green peels of Juglans mandshurica Maxim.
Solvent: Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, etc.
Download: COA    MSDS
Similar structural: Comparison (Web)  (SDF)
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Size /Price /Stock 10 mM * 1 mL in DMSO / Inquiry
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Biological Activity
Description: 7-Methoxy-1-tetralone may have insecticidal activity.
In vitro:
Journal of Forestry Research, 2007,18 (1) :62-4.
Insecticidal activities and active components of the alcohol extract from green peel of Juglans mandshurica[Reference: WebLink]

METHODS AND RESULTS:
The extract of green peel of Juglans mandshurica Maxim was extracted by common method for studying its insecticidal activities and analyzing the active components. Results showed that the alcohol extract and the chloroform part of extract (separated with chloroform from alcohol extract) form green peel of J. mandshurica have insecticidal activities in contact toxicity and stomach toxicity against larvae of Lymantria dispar L.. After application of the extracts for five days, the corrected mortality of larvae of Lymantria dispar for both extracts was more than 50% in contact toxicity and stomach toxicity at the concentration of ≥ 5 g·L-1. The insecticidal activity for both alcohol extract and chloroform part of extract is more effect in contact toxicity than in stomach toxicity, but no significant difference in the insecticidal activities was found between alcohol extract and chloroform part of extract. The active components in the chloroform part of extract from green peel of J. mandshurica were analyzed by GC-MS.
CONCLUSIONS:
The analyzed results showed that the active components in the chloroform part of extract are: (1) juglone (5-hydroxy-1,4-naphthaoquinone), the relative content 27.11%, (2) 1,5-Naphthalenediol, the relative content 9.52%, (3) 7-Methoxy-1-tetralone, the relative content 6.81%, (4) Benzofuran, 2,3-dihydro-, the relative content 6.76%, (5) 4-Hydroxy-2-methoxycinnamaldehyde, the relative content 3.99%, (6) 2-Methoxy-4-vinylphenol, the relative content 3.05%.
7-Methoxy-1-tetralone Description
Source: The green peels of Juglans mandshurica Maxim.
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.

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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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Calculate Dilution Ratios(Only for Reference)
1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 5.675 mL 28.3752 mL 56.7505 mL 113.5009 mL 141.8762 mL
5 mM 1.135 mL 5.675 mL 11.3501 mL 22.7002 mL 28.3752 mL
10 mM 0.5675 mL 2.8375 mL 5.675 mL 11.3501 mL 14.1876 mL
50 mM 0.1135 mL 0.5675 mL 1.135 mL 2.27 mL 2.8375 mL
100 mM 0.0568 mL 0.2838 mL 0.5675 mL 1.135 mL 1.4188 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.
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