o-Cresolphthalein - Ind, high purity , CAS No.596-27-0

Item Number
C305618
Grouped product items
SKUSizeAvailabilityPrice Qty
C305618-1g
1g
In stock
$51.90

Basic Description

Synonymso-Cresolphthalein | 596-27-0 | 1(3H)-Isobenzofuranone, 3,3-bis(4-hydroxy-3-methylphenyl)- | 3,3-Bis(4-hydroxy-3-methylphenyl)isobenzofuran-1(3H)-one | 3',3''-Dimethylphenolphthalein | 3,3-bis(4-hydroxy-3-methylphenyl)-2-benzofuran-1-one | Phenolphthalein, 3',3''-dime
Specifications & Purityindicator
Biochemical and Physiological MechanismsO-cresol phthalein is a reversible pH indicator. The kinetics of the reverse path (red-purple to colorless) is slow, which makes it an appropriate molecule to check the flow pattern in corrugated wall tubes. It is also used for colorimetric determination
Storage TempDesiccated
Shipped InNormal
Gradeindicator
Note卖完停产,不再备货
Product Description

Soluble in ethanol, ether and glacial acetic acid, purple in dilute alkali, slightly soluble in water and hardly soluble in benzene.
O-Cresolphthalein has been used as a component in calcifying media for calcification assay.

Associated Targets(Human)

POLB Tchem DNA polymerase beta (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
EHMT2 Tchem Histone-lysine N-methyltransferase EHMT2 (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
GMNN Tbio Geminin (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
POLH Tchem DNA polymerase eta (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
RAPGEF4 Tchem Rap guanine nucleotide exchange factor 4 (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
KMT2A Tchem Histone-lysine N-methyltransferase 2A (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
SMN1 Tchem Survival motor neuron protein (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
SMAD3 Tchem Mothers against decapentaplegic homolog 3 (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
POLI Tchem DNA polymerase iota (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
L3MBTL1 Tchem Lethal(3)malignant brain tumor-like protein 1 (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
LMNA Tbio Prelamin-A/C (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
BAZ2B Tchem Bromodomain adjacent to zinc finger domain protein 2B (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
TDP1 Tchem Tyrosyl-DNA phosphodiesterase 1 (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
APEX1 Tchem DNA-(apurinic or apyrimidinic site) lyase (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
MAPT Tclin Microtubule-associated protein tau (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
GLP1R Tclin Glucagon-like peptide 1 receptor (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
IDH1 Tclin Isocitrate dehydrogenase [NADP] cytoplasmic (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
KDM4A Tchem Lysine-specific demethylase 4A (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
POLB Tchem DNA polymerase beta (23632 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
GLP1R Tclin Glucagon-like peptide 1 receptor (111429 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
POLI Tchem DNA polymerase iota (116820 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
POLH Tchem DNA polymerase eta (21678 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
KDM4A Tchem Lysine-specific demethylase 4A (52245 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
APEX1 Tchem DNA-(apurinic or apyrimidinic site) lyase (38016 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
EHMT2 Tchem Histone-lysine N-methyltransferase, H3 lysine-9 specific 3 (93046 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
TDP1 Tchem Tyrosyl-DNA phosphodiesterase 1 (345557 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
L3MBTL1 Tchem Lethal(3)malignant brain tumor-like protein 1 (14536 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SMN1 Tchem Survival motor neuron protein (34246 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
LMNA Tbio Prelamin-A/C (36751 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SMAD3 Tchem Mothers against decapentaplegic homolog 3 (68039 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
GMNN Tbio Geminin (128009 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
BAZ2B Tchem Bromodomain adjacent to zinc finger domain protein 2B (56204 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
IDH1 Tclin Isocitrate dehydrogenase [NADP] cytoplasmic (40980 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
RAPGEF4 Tchem Rap guanine nucleotide exchange factor 4 (11476 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

Plasmodium falciparum (966862 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
TGR Thioredoxin glutathione reductase (28579 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mapt Microtubule-associated protein tau (6 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Mechanisms of Action

Mechanism of ActionAction Typetarget IDTarget NameTarget TypeTarget OrganismBinding Site NameReferences

Names and Identifiers

IUPAC Name 3,3-bis(4-hydroxy-3-methylphenyl)-2-benzofuran-1-one
INCHI InChI=1S/C22H18O4/c1-13-11-15(7-9-19(13)23)22(16-8-10-20(24)14(2)12-16)18-6-4-3-5-17(18)21(25)26-22/h3-12,23-24H,1-2H3
InChi Key CPBJMKMKNCRKQB-UHFFFAOYSA-N
Canonical SMILES CC1=C(C=CC(=C1)C2(C3=CC=CC=C3C(=O)O2)C4=CC(=C(C=C4)O)C)O
Isomeric SMILES CC1=C(C=CC(=C1)C2(C3=CC=CC=C3C(=O)O2)C4=CC(=C(C=C4)O)C)O
WGK Germany 3
PubChem CID 68995
Molecular Weight 346.38
Beilstein 310554

Certificates

Certificate of Analysis(COA)

Enter Lot Number to search for COA:

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

5 results found

Lot NumberCertificate TypeDateItem
G2313384Certificate of AnalysisJun 28, 2023 C305618
G2313385Certificate of AnalysisJun 28, 2023 C305618
G2313389Certificate of AnalysisJun 28, 2023 C305618
G2313394Certificate of AnalysisJun 28, 2023 C305618
G2313396Certificate of AnalysisJun 28, 2023 C305618

Chemical and Physical Properties

Melt Point(°C)223-225°C

Safety and Hazards(GHS)

WGK Germany 3

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Citations of This Product

1. Fan Yang, Hongbo Yu, Chunzheng Wu, Shiwei Wang, Tong Li, Hongfeng Yin.  (2022)  RhCu Bimetallic Nanoparticles in Hollow Carbon Spheres for Catalytic Halonitrobenzene Chemoselective Hydrogenation.  ACS Applied Nano Materials,  (8): (11627–11635).  [PMID:] [10.1021/acsanm.2c02358]
2. Yongmei Tang, Lan Li, Kai Ma, Guofei Chen, Wei Wang, Xingzhong Fang.  (2018)  Transparent and organosoluble cardo polyimides with different trans/cis ratios of 1,4-diaminocyclohexane via aromatic nucleophilic substitution polymerization.  POLYMER INTERNATIONAL,  67  (5): (598-605).  [PMID:] [10.1002/pi.5556]
3. Nafeesa Mushtaq, Lala Rukh Sidra, Guofei Chen, Yongmei Tang, Lubo Xu, Xingzhong Fang.  (2017)  Synthesis of cardo containing asymmetric poly(ether-naphthalimide-phthalimide)s.  POLYMER INTERNATIONAL,  66  (11): (1633-1639).  [PMID:] [10.1002/pi.5425]
4. Leiduan Hao, Yanfei Zhao, Bo Yu, Hongye Zhang, Huanjun Xu, Jilei Xu, Zhimin Liu.  (2014)  Polyurea-supported metal nanocatalysts: Synthesis, characterization and application in selective hydrogenation of o-chloronitrobenzene.  JOURNAL OF COLLOID AND INTERFACE SCIENCE,  424  (44).  [PMID:24767496] [10.1016/j.jcis.2014.03.015]

References

1. Fan Yang, Hongbo Yu, Chunzheng Wu, Shiwei Wang, Tong Li, Hongfeng Yin.  (2022)  RhCu Bimetallic Nanoparticles in Hollow Carbon Spheres for Catalytic Halonitrobenzene Chemoselective Hydrogenation.  ACS Applied Nano Materials,  (8): (11627–11635).  [PMID:] [10.1021/acsanm.2c02358]
2. Yongmei Tang, Lan Li, Kai Ma, Guofei Chen, Wei Wang, Xingzhong Fang.  (2018)  Transparent and organosoluble cardo polyimides with different trans/cis ratios of 1,4-diaminocyclohexane via aromatic nucleophilic substitution polymerization.  POLYMER INTERNATIONAL,  67  (5): (598-605).  [PMID:] [10.1002/pi.5556]
3. Nafeesa Mushtaq, Lala Rukh Sidra, Guofei Chen, Yongmei Tang, Lubo Xu, Xingzhong Fang.  (2017)  Synthesis of cardo containing asymmetric poly(ether-naphthalimide-phthalimide)s.  POLYMER INTERNATIONAL,  66  (11): (1633-1639).  [PMID:] [10.1002/pi.5425]
4. Leiduan Hao, Yanfei Zhao, Bo Yu, Hongye Zhang, Huanjun Xu, Jilei Xu, Zhimin Liu.  (2014)  Polyurea-supported metal nanocatalysts: Synthesis, characterization and application in selective hydrogenation of o-chloronitrobenzene.  JOURNAL OF COLLOID AND INTERFACE SCIENCE,  424  (44).  [PMID:24767496] [10.1016/j.jcis.2014.03.015]

Solution Calculators