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Merck
CN

Y0000493

Phloroglucinol (anhydrous)

European Pharmacopoeia (EP) Reference Standard

Synonym(s):

Phloroglucinol, 1,3,5-Trihydroxybenzene

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About This Item

Empirical Formula (Hill Notation):
C6H6O3
CAS Number:
Molecular Weight:
126.11
UNSPSC Code:
41116107
NACRES:
NA.24
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
1341907
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Product Name

Phloroglucinol (anhydrous), European Pharmacopoeia (EP) Reference Standard

InChI

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

SMILES string

Oc1cc(O)cc(O)c1

InChI key

QCDYQQDYXPDABM-UHFFFAOYSA-N

grade

pharmaceutical primary standard

API family

phloroglucinol

manufacturer/tradename

EDQM

application(s)

pharmaceutical (small molecule)

format

neat

storage temp.

2-8°C

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Application

Phloroglucinol (anhydrous) EP Reference standard, intended for use in laboratory tests only as specifically prescribed in the European Pharmacopoeia.

General description

This product is provided as delivered and specified by the issuing Pharmacopoeia. All information provided in support of this product, including SDS and any product information leaflets have been developed and issued under the Authority of the issuing Pharmacopoeia.For further information and support please go to the website of the issuing Pharmacopoeia.

Other Notes

Sales restrictions may apply.

Packaging

The product is delivered as supplied by the issuing Pharmacopoeia. For the current unit quantity, please visit the EDQM reference substance catalogue.

pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - Skin Sens. 1 - STOT SE 3

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk

WGK 2

flash_point_f

Not applicable

flash_point_c

Not applicable

Regulatory Information

危险化学品
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Fang Yang et al.
Applied microbiology and biotechnology, 93(2), 487-495 (2011-11-22)
Phloroglucinol derivatives are a major class of secondary metabolites of wide occurrence in biological systems. In the bacteria kingdom, these compounds can only be synthesized by some species of Pseudomonads. Pseudomonas spp. could produce 2,4-diacetylphloroglucinol (DAPG) that plays an important
Inder Pal Singh et al.
Expert opinion on therapeutic patents, 19(6), 847-866 (2009-05-29)
Phloroglucinol compounds, both synthetic as well as natural, have shown a vast array of biological activities. There are a wide range of applications of phloroglucinol compounds in pharmaceuticals, cosmetics, textiles, paints and dyeing industries. Although many of the phloroglucinols have
Phloroglucinol compounds of natural origin.
Inder Pal Singh et al.
Natural product reports, 23(4), 558-591 (2006-07-29)
Inder Pal Singh et al.
Natural product reports, 27(3), 393-416 (2010-02-25)
This review covers the synthetic aspects of various naturally occurring phloroglucinols, describing syntheses of 42 compounds and citing 137 references.
Hong Zhang et al.
Journal of natural products, 77(7), 1700-1707 (2014-06-25)
Five new prenylated benzoylphloroglucinol derivatives, garciesculentones A-E (1-5), a new xanthone, garciesculenxanthone A (6), and 15 known compounds were isolated from the petroleum ether extract and the EtOAc-soluble fraction of a 80% (v/v) EtOH extract of Garcinia esculenta. The structures

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