Skip to Content
Merck
CN

61419

Isopimpinellin

analytical standard

Synonym(s):

4,9-Dimethoxy-7H-furo[3,2-g][1]benzopyran-7-one, 4,9-Dimethoxyfuro[3,2-g]chromen-7-one, 5,8-Dimethoxy-6,7-furanocoumarin, 5,8-Dimethoxypsoralen, Isoimpinellin, NSC 217988, NSC 401288

Sign In to View Organizational & Contract Pricing.

Select a Size

About This Item

Empirical Formula (Hill Notation):
C13H10O5
CAS Number:
482-27-9
Molecular Weight:
246.22
UNSPSC Code:
85151701
NACRES:
NA.24
PubChem Substance ID:
329759487
MDL number:
MFCD00017407
Beilstein/REAXYS Number:
262337

Key Documents

View All Documentation
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist

InChI key

DFMAXQKDIGCMTL-UHFFFAOYSA-N

InChI

1S/C13H10O5/c1-15-10-7-3-4-9(14)18-12(7)13(16-2)11-8(10)5-6-17-11/h3-6H,1-2H3

grade

analytical standard

assay

≥95.0% (HPLC)

shelf life

limited shelf life, expiry date on the label

impurities

≤5.0% water

application(s)

food and beverages

format

neat

storage temp.

2-8°C

Quality Level

100

Looking for similar products? Visit Product Comparison Guide

General description

Isopimpinellin is a furanocoumarin which is synthesized by a variety of plant species. It is known to exhibit antimicrobial, antioxidant and anti-biofilm activities.

Application

Isopimpinellin may be used as an analytical reference standard for the determination of the analyte in pharmaceutical formulations, rat plasma, parsley herb extracts and Heracleum sibiricum L. fruits by chromatography based techniques.

Other Notes

Find a digital Reference Material for this product available on our online platform ChemisTwin® for NMR. You can use this digital equivalent on ChemisTwin® for your sample identity confirmation and compound quantification (with digital external standard). An NMR spectrum of this substance can be viewed and an online comparison against your sample can be performed with a few mouseclicks. Learn more here and start your free trial.

pictograms

Skull and crossbones
GHS06

signalword

Danger

Hazard Classifications

Acute Tox. 2 Dermal - Acute Tox. 2 Inhalation - Acute Tox. 2 Oral

Storage Class

6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
BCCJ3104
BCCH6816
BCCH2882
BCCG2627
BCCG1132

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Search for a COA

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

C A Cardoso et al.
Journal of pharmaceutical and biomedical analysis, 22(2), 203-214 (2000-03-17)
A solid-phase extraction and chromatography-flame ionization detection (GC-FID) method has been developed for the routine analysis of psoralen, bergapten, isopimpinellin and pimpinellin in creams and pomades employed in Brazil for the treatment of vitiligo. The calibration curve for psoralen was
Simultaneous determination of pimpinellin, isopimpinellin and phellopterin in rat plasma by a validated UPLC--MS/MS and its application to a pharmacokinetic study after administration of Toddalia asiatica extract
Liu Z, et al.
Journal of Chromatography. B, Biomedical Sciences and Applications, 891, 102-108 (2012)
Ya-Wen Cheng et al.
Cell reports, 33(2), 108254-108254 (2020-10-03)
Development of specific antiviral agents is an urgent unmet need for SARS-coronavirus 2 (SARS-CoV-2) infection. This study focuses on host proteases that proteolytically activate the SARS-CoV-2 spike protein, critical for its fusion after binding to angiotensin-converting enzyme 2 (ACE2), as
The analysis of furanocoumarins in fruits of Heracleum sibiricum L
Bogucka-Kocka, ANNA
Acta Poloniae Pharmaceutica, 56(5), 399-402 (1999)
Linear furanocoumarins and graveolone from the common herb parsley
Beier RC, et al.
Phytochemistry, 36(4), 869-872 (1994)
View All Related Papers

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service