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Merck

P1178

Phloroglucinol

BioReagent, suitable for plant cell culture

Synonym(s):

1,3,5-Trihydroxybenzene

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About This Item

Empirical Formula (Hill Notation):
C6H6O3
CAS Number:
Molecular Weight:
126.11
UNSPSC Code:
10171502
NACRES:
NA.72
PubChem Substance ID:
EC Number:
203-611-2
Beilstein/REAXYS Number:
1341907
MDL number:

Product Name

Phloroglucinol, BioReagent, suitable for plant cell culture

InChI key

QCDYQQDYXPDABM-UHFFFAOYSA-N

InChI

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

SMILES string

Oc1cc(O)cc(O)c1

product line

BioReagent

form

powder

technique(s)

cell culture | plant: suitable

application(s)

agriculture

Quality Level

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Application

Phloroglucinol has been used to prevent hyperhydricity by promoting lignification of shoots. It has also been used in PG (phloroglucinol)-sucrose treatments for growth and development of in vitro derived shoot tips.

General description

Phloroglucinol is a trihydroxybenzene with antithrombotic, profibrinolytic, antimicrobial, antimalarial, cancer chemopreventive, anti-HIV and anti-leishmanial activities. Phloroglucinol (PG) is a biosynthetic precursor of the 2,4-diacetylphloroglucinol (DAPG) an antibiotic against soil-borne diseases. Phloroglucinol is a useful intermediate because it is polyfunctional.

pictograms

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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

ppe

Eyeshields, Gloves, type N95 (US)


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In vitro propagation of `Guayabo del pais?(Acca sellowiana (Berg.) Burret)
Ross S and Grasso R
Fruit, Vegetable and Cereal Science and Biotechnology, 4(1), 83-87 (2010)
Phloroglucinol enhances growth and rate of axillary shoot proliferation in potato shoot tip cultures in vitro
Sarkar D and Naik P S
Plant Cell, Tissue and Organ Culture, 60(2), 139-149 (2000)
Yong Li et al.
Bioorganic & medicinal chemistry, 17(5), 1963-1973 (2009-02-10)
Seven phlorotannins were isolated and characterized from an edible marine brown alga Ecklonia cava (EC), along with three common sterol derivatives (fucosterol, ergosterol, and cholesterol) according to the comprehensive spectral analysis of MS and NMR data. Compounds 5 (7-phloro eckol)
Liva Harinantenaina et al.
Journal of natural products, 76(3), 388-393 (2013-01-05)
Bioassay-guided fractionation of an ethanol extract of the leaves and inflorescence of Mallotus oppositifolius collected in Madagascar led to the isolation of the two new bioactive dimeric phloroglucinols mallotojaponins B (1) and C (2), together with the known mallotophenone (3).
Phloroglucinol compounds of natural origin.
Inder Pal Singh et al.
Natural product reports, 23(4), 558-591 (2006-07-29)

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