Skip to Content
Merck
CN
All Photos(1)

Key Documents

61419

Supelco

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 Into View Organizational & Contract Pricing


About This Item

Empirical Formula (Hill Notation):
C13H10O5
CAS Number:
Molecular Weight:
246.22
Beilstein:
262337
MDL number:
UNSPSC Code:
85151701
PubChem Substance ID:
NACRES:
NA.24

grade

analytical standard

Quality Level

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

SMILES string

O=C1OC2=C(OC)C3=C(C=CO3)C(OC)=C2C=C1

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

InChI key

DFMAXQKDIGCMTL-UHFFFAOYSA-N

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.

Recommended products

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

Signal Word

Danger

Hazard Statements

Hazard Classifications

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

Storage Class Code

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

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.

Already Own This Product?

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

Visit the Document Library

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
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)
Xiaoxue Wu et al.
Molecules (Basel, Switzerland), 24(24) (2019-12-11)
Cnidium monnieri (L.) Cusson is a popular Traditional Chinese Medicine (TCM) with a variety of bioactivities. However, there are some problems that have affected the development of Cnidium monnieri (L.) Cusson. At present, many methods have been reported for the
Linear furanocoumarins and graveolone from the common herb parsley
Beier RC, et al.
Phytochemistry, 36(4), 869-872 (1994)
The analysis of furanocoumarins in fruits of Heracleum sibiricum L
Bogucka-Kocka, ANNA
Acta Poloniae Pharmaceutica, 56(5), 399-402 (1999)

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