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Phloroglucinol Anhydrous - for plant cell culture, >99.0% (HPLC), high purity , Voltage-gated calcium channel blocker, CAS No.108-73-6, Voltage-gated calcium channel blocker

In stock
Item Number
P104098
Grouped product items
SKU Size
Availability
Price Qty
P104098-25g
25g
2
$111.90
P104098-100g
100g
1
$301.90

Basic Description

Synonyms phloroglucinol | 108-73-6 | Benzene-1,3,5-triol | 1,3,5-trihydroxybenzene | Phloroglucin | 1,3,5-benzenetriol | Phloroglucine | Spasfon-Lyoc | Dilospan S | sym-Trihydroxybenzene | s-Trihydroxybenzene | Benzene-s-triol | 5-Hydroxyresorcinol | Benzene, trihydroxy | 5-Oxyresorcinol | 3,5
Specifications & Purity for plant cell culture, ≥99%(HPLC)
Storage Temp Protected from light,Room temperature
Shipped In Normal
Grade for plant cell culture
Action Type BLOCKER
Mechanism of action Voltage-gated calcium channel blocker
Product Description

Phloroglucinol is a hygroscopic biochemical that is also potentially useful for bone decalcification in microscopy specimens or the detection of wood fibers.
A potentially useful hygroscopic biochemical.

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
Superclass Benzenoids
Class Phenols
Subclass Benzenetriols and derivatives
Intermediate Tree Nodes Not available
Direct Parent Phloroglucinols and derivatives
Alternative Parents 1-hydroxy-4-unsubstituted benzenoids  1-hydroxy-2-unsubstituted benzenoids  Benzene and substituted derivatives  Polyols  Hydrocarbon derivatives  
Molecular Framework Aromatic homomonocyclic compounds
Substituents Phloroglucinol derivative - 1-hydroxy-4-unsubstituted benzenoid - 1-hydroxy-2-unsubstituted benzenoid - Monocyclic benzene moiety - Polyol - Organic oxygen compound - Hydrocarbon derivative - Organooxygen compound - Aromatic homomonocyclic compound
Description This compound belongs to the class of organic compounds known as phloroglucinols and derivatives. These are compounds containing a phloroglucinol (benzene-1,3,5-triol) moiety, which consists of a benzene ring bearing one hydroxyl group at positions 1,3, and 5.
External Descriptors a small molecule

Product Properties

ALogP 0.2

Associated Targets(Human)

TYR Tclin Tyrosinase (717 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
PTGS1 Tclin Cyclooxygenase-1 (9233 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
BACE1 Tchem Beta-secretase 1 (15641 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
HL-60 (67320 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
HT-1080 (3966 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
MRC5 (9203 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
POLK Tbio DNA polymerase kappa (8653 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID

Associated Targets(non-human)

Hdac6 Histone deacetylase 6 (222 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Crotalus adamanteus (3 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
RAW264.7 (28094 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Vero (26788 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
rep Replicase polyprotein 1ab (378 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID

Mechanisms of Action

Mechanism of Action Action Type target ID Target Name Target Type Target Organism Binding Site Name References

Names and Identifiers

Pubchem Sid 504750383
Pubchem Sid Url https://pubchem.ncbi.nlm.nih.gov/substance/504750383
IUPAC Name benzene-1,3,5-triol
INCHI InChI=1S/C6H6O3/c7-4-1-5(8)3-6(9)2-4/h1-3,7-9H
InChIKey QCDYQQDYXPDABM-UHFFFAOYSA-N
Smiles C1=C(C=C(C=C1O)O)O
Isomeric SMILES C1=C(C=C(C=C1O)O)O
WGK Germany 2
Molecular Weight 126.11
Beilstein 1341907
Reaxy-Rn 1341907
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1341907&ln=

Certificates(CoA,COO,BSE/TSE and Analysis Chart)

C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

5 results found

Lot Number Certificate Type Date Item
J2313388 Certificate of Analysis Sep 21, 2023 P104098
J2313387 Certificate of Analysis Sep 21, 2023 P104098
E2520095 Certificate of Analysis Sep 21, 2023 P104098
C1615078 Certificate of Analysis Aug 15, 2023 P104098
K2010296 Certificate of Analysis Sep 12, 2022 P104098

Chemical and Physical Properties

Solubility Soluble in water (10 g/l at 20 °C), ethanol, ether, pyridine, and methanol.
Sensitivity Light sensitive.
Boil Point(°C) 218°C
Melt Point(°C) 215-220 °C
Molecular Weight 126.110 g/mol
XLogP3 0.200
Hydrogen Bond Donor Count 3
Hydrogen Bond Acceptor Count 3
Rotatable Bond Count 0
Exact Mass 126.032 Da
Monoisotopic Mass 126.032 Da
Topological Polar Surface Area 60.700 Ų
Heavy Atom Count 9
Formal Charge 0
Complexity 63.300
Isotope Atom Count 0
Defined Atom Stereocenter Count 0
Undefined Atom Stereocenter Count 0
Defined Bond Stereocenter Count 0
Undefined Bond Stereocenter Count 0
The total count of all stereochemical bonds 0
Covalently-Bonded Unit Count 1

Alternative Products

Citations of This Product

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7. Min Zhang, Yiguo Jiang, Xiuquan Xu, Xiaofeng Yu, Wenyan Shen, Miaomiao Luo, Luyao Ding, Haiwen Chen.  (2022)  Facile synthesis of porous 1,3,5-Trihydroxybenzene substituted g-C3N4 for boosted photocatalytic Rhodamine B degradation and H2O2 production.  JOURNAL OF ALLOYS AND COMPOUNDS,  925  (166604). 
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