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Perillen
Perillen
ChemFaces products have been cited in many studies from excellent and top scientific journals
Product Name Perillen
Price: $168 / 20mg
CAS No.: 539-52-6
Catalog No.: CFN90862
Molecular Formula: C10H14O
Molecular Weight: 150.2 g/mol
Purity: >=98%
Type of Compound: Alkaloids
Physical Desc.: Oil
Source: The herbs of Perilla frutescens.
Solvent: Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, etc.
Download: COA    MSDS    SDF
Similar structural: Comparison (Web)  (SDF)
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According to end customer requirements, ChemFaces provide solvent format. This solvent format of product intended use: Signaling Inhibitors, Biological activities or Pharmacological activities.
Size /Price /Stock 10 mM * 1 mL in DMSO / $32.1 / In-stock
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Product Use Citation
Related Screening Libraries
Size /Price /Stock 10 mM * 100 uL in DMSO / Inquiry / In-stock
10 mM * 1 mL in DMSO / Inquiry / In-stock
Related Libraries
Biological Activity
Description: Perillen is a nartural product from Perilla frutescens.
Perillen Description
Source: The herbs of Perilla frutescens.
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
More...

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 6.6578 mL 33.2889 mL 66.5779 mL 133.1558 mL 166.4447 mL
5 mM 1.3316 mL 6.6578 mL 13.3156 mL 26.6312 mL 33.2889 mL
10 mM 0.6658 mL 3.3289 mL 6.6578 mL 13.3156 mL 16.6445 mL
50 mM 0.1332 mL 0.6658 mL 1.3316 mL 2.6631 mL 3.3289 mL
100 mM 0.0666 mL 0.3329 mL 0.6658 mL 1.3316 mL 1.6644 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:
Insect Biochemistry, 1980 , 10 (1) :107-12.
A comparative analysis of mandibular gland secretions in the ant tribe tetramoriini.[Reference: WebLink]

METHODS AND RESULTS:
Chemical analysis of the mandibular gland secretion of seven ant species in the tribe Tetramoriini showed that 3-octanone was the major component in Tetramorium sericeiventre (70%), T. caespitum (71%) and T. guineense (87%), and 3-octanol in Decamorium uelense (96%). 2-Undecanol, was the major component in T. termitobium (80%), but in two members of the subgenus Xiphomyrmex, T. angulinode and an unidentified species (D), the sesquiterpene furan, Perillen, was predominant (91% and 98% respectively). Ants in this subgenus also contained 2-nonanol, 2-undecanol and 2-undecanone in their mandibular glands.
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CFN89539Acetylatractylodinol61582-39-6240.25C15H12O3
CFN94243Furan110-00-968.07C4H4O
CFN97598Furan-2-carboxylic acid88-14-2112.08C5H4O3
CFN96899Furan-3-carboxylic acid488-93-7112.08C5H4O3
CFN930665-Methyl-2-furaldehyde620-02-0110.1C6H6O2
CFN971495-Hydroxymethylfurfural67-47-0126.1 C6H6O3
CFN957255-[(alpha-D-galactopyranosyloxy)methyl]-1H-pyrrole-2-carbaldehyde1377977-55-3287.3C12H17NO7
CFN957205-(alpha-D-galactopyranosyloxymethyl)-2-furancarboxaldehyde890652-72-9288.3C12H16O8
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