Skip to Content
Merck
All Photos(2)

Key Documents

06931

Supelco

Pyrogallol

analytical standard

Synonym(s):

1,2,3-Trihydroxybenzene, 2,3-Dihydroxyphenol, Pyrogallic acid

Sign Into View Organizational & Contract Pricing


About This Item

Linear Formula:
C6H3(OH)3
CAS Number:
Molecular Weight:
126.11
Beilstein:
907431
EC Number:
MDL number:
UNSPSC Code:
85151701
PubChem Substance ID:
NACRES:
NA.24

grade

analytical standard

Quality Level

vapor density

4.4 (vs air)

vapor pressure

10 mmHg ( 167.7 °C)

Assay

≥98.0% (HPLC)

shelf life

limited shelf life, expiry date on the label

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

impurities

≤0.5% water

bp

309 °C (lit.)

mp

132-134 °C
133-134 °C (lit.)

application(s)

cleaning products
cosmetics
food and beverages
personal care

format

neat

storage temp.

2-8°C

SMILES string

Oc1cccc(O)c1O

InChI

1S/C6H6O3/c7-4-2-1-3-5(8)6(4)9/h1-3,7-9H

InChI key

WQGWDDDVZFFDIG-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

General description

Pyrogallol is a phenolic allelochemical, a catechin compound with a defensive mode of action against invading microbes. It is an active component of Emblica officinalis extracts with an anti-proliferative effect on non-small cell lung cancer (NSCLC). Pyrogallol is also reported to be algicidal and is known to inhibit the growth of harmful cyanobacteria/algae.

Application

Pyrogallol may be used as an analytical standard for the determination of the analyte in biological matrices by gas chromatography/mass spectrometry (GC/MS) and in beverages by flow-injection chemiluminescent method.

Packaging

Bottomless glass bottle. Contents are inside inserted fused cone.

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

Health hazardExclamation mark

Signal Word

Warning

Hazard Classifications

Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Aquatic Chronic 3 - Muta. 2

Storage Class Code

13 - Non Combustible Solids

WGK

WGK 2

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

Customers Also Viewed

Antimicrobial activity of catechol and pyrogallol as allelochemicals
Kocacal?skanismailkc I, et al.
Zeitschrift fur Naturforschung C, 61(9-10), 639-642 (2006)
GC/MS determination of pyrogallol and gallic acid in biological matrices as diagnostic indicators of oak exposure
Tor ER, et al.
Journal of Agricultural and Food Chemistry, 44(5), 1275-1279 (1996)
Allelopathic mechanism of pyrogallol to Microcystis aeruginosa PCC7806 (Cyanobacteria): from views of gene expression and antioxidant system
Shao J, et al.
Chemosphere, 75(7), 924-928 (2009)
Adelaide U P Hain et al.
Journal of structural biology, 180(3), 551-562 (2012-09-18)
The autophagy-related proteins are thought to serve multiple functions in Plasmodium and are considered essential to parasite survival and development. We have studied two key interacting proteins, Atg8 and Atg3, of the autophagy pathway in Plasmodium falciparum. These proteins are
Suzanne J P L van den Berg et al.
Chemical research in toxicology, 25(11), 2352-2367 (2012-09-21)
The present study describes physiologically based kinetic (PBK) models for the alkenylbenzene elemicin (3,4,5-trimethoxyallylbenzene) in rat and human, based on the PBK models previously developed for the structurally related alkenylbenzenes estragole, methyleugenol, and safrole. Using the newly developed models, the

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