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Bisphenol A - >99.0%(GC), high purity , CAS No.80-05-7, Antagonist of Androgen receptor;Agonist of Estrogen receptor-β

  • Moligand™
  • ≥99%(GC)
Item Number
B108652
Grouped product items
SKUSizeAvailabilityPrice Qty
B108652-25g
25g
Available within 4-8 weeks(?)
Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!
$9.90
B108652-100g
100g
Available within 4-8 weeks(?)
Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!
$15.90
B108652-500g
500g
In stock
$23.90

Basic Description

SynonymsBisphenol A|80-05-7|2,2-Bis(4-hydroxyphenyl)propane|4,4'-Isopropylidenediphenol|Diphenylolpropane|4,4'-Bisphenol A|Bisphenol|Diano|Bisphenol-A|4,4'-(propane-2,2-diyl)diphenol|Biphenol A|Parabis A|2,2-Bis(p-hydroxyphenyl)propane|DIAN|p,p'-Isopropylidenebis
Specifications & PurityMoligand™, ≥99%(GC)
Shipped InNormal
GradeMoligand™
Action TypeAGONIST, ANTAGONIST
Mechanism of actionAntagonist of Androgen receptor;Agonist of Estrogen receptor-β

Associated Targets

CYP1A2 Tchem Cytochrome P450 1A2 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

DRD2 Tclin D(2) dopamine receptor 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

DRD4 Tchem D(4) dopamine receptor 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

CYP3A4 Tclin Cytochrome P450 3A4 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

ERBB2 Tclin Receptor tyrosine-protein kinase erbB-2 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

ELANE Tclin Neutrophil elastase 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

EGFR Tclin Epidermal growth factor receptor 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

AVPR1A Tclin Vasopressin V1a receptor 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

HMGCR Tclin 3-hydroxy-3-methylglutaryl-coenzyme A reductase 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

HDAC6 Tclin Histone deacetylase 6 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

HRH1 Tclin Histamine H1 receptor 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

SLC6A3 Tclin Sodium-dependent dopamine transporter 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

SLC6A4 Tclin Sodium-dependent serotonin transporter 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

SIGMAR1 Tclin Sigma non-opioid intracellular receptor 1 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

PTGS1 Tclin Prostaglandin G/H synthase 1 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

CACNA1C Tclin Voltage-dependent L-type calcium channel subunit alpha-1C 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

CA2 Tclin Carbonic anhydrase 2 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

DRD3 Tclin D(3) dopamine receptor 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

CHRM3 Tclin Muscarinic acetylcholine receptor M3 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

CHRM4 Tclin Muscarinic acetylcholine receptor M4 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

ADRA2B Tclin Alpha-2B adrenergic receptor 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

ADRA2C Tclin Alpha-2C adrenergic receptor 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

HTR2A Tclin 5-hydroxytryptamine receptor 2A 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

ADORA2A Tclin Adenosine receptor A2a 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

ACHE Tclin Acetylcholinesterase 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

ADRA1B Tclin Alpha-1B adrenergic receptor 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

ADRA1A Tclin Alpha-1A adrenergic receptor 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

AR Tclin Androgen receptor 1 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

MAOA Tclin Amine oxidase [flavin-containing] A 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

AKR1B1 Tclin Aldose reductase 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

ADORA1 Tclin Adenosine receptor A1 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

HTR1A Tclin 5-hydroxytryptamine receptor 1A 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

ADORA3 Tchem Adenosine receptor A3 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

HTR6 Tchem 5-hydroxytryptamine receptor 6 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

HTR2B Tclin 5-hydroxytryptamine receptor 2B 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

CLK3 Tchem Dual specificity protein kinase CLK3 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

CLK1 Tchem Dual specificity protein kinase CLK1 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

EDNRA Tclin Endothelin-1 receptor 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

GSK3B Tclin Glycogen synthase kinase-3 beta 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

KCNH2 Tclin Potassium voltage-gated channel subfamily H member 2 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

OPRD1 Tclin Delta-type opioid receptor 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

OPRK1 Tclin Kappa-type opioid receptor 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

OPRM1 Tclin Mu-type opioid receptor 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

NOS2 Tchem Nitric oxide synthase, inducible 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

TACR1 Tclin Substance-P receptor 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

NOS1 Tchem Nitric oxide synthase, brain 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

Names and Identifiers

IUPAC Name 4-[2-(4-hydroxyphenyl)propan-2-yl]phenol
INCHI InChI=1S/C15H16O2/c1-15(2,11-3-7-13(16)8-4-11)12-5-9-14(17)10-6-12/h3-10,16-17H,1-2H3
InChi Key IISBACLAFKSPIT-UHFFFAOYSA-N
Canonical SMILES CC(C)(C1=CC=C(C=C1)O)C2=CC=C(C=C2)O
Isomeric SMILES CC(C)(C1=CC=C(C=C1)O)C2=CC=C(C=C2)O
WGK Germany 2
RTECS SL6300000
Alternate CAS 80-05-7,2444-90-8 (di-hydrochloride salt)
PubChem CID 6623
NSC Number 1767
UN Number 3077(international)
Packing Group III
MeSH Entry Terms 2,2-bis(4-hydroxyphenyl)propane;4,4'-dihydroxy-2,2-diphenylpropane;bisphenol A;bisphenol A, disodium salt;bisphenol A, sodium salt;diphenylolpropane
Molecular Weight 228.29
Beilstein 1107700

Certificates

Certificate of Analysis(COA)

Enter Lot Number to search for COA:

To view the certificate results,please click on a Lot number.For Lot numbers from past orders,please use our order status section

23 results found

Lot NumberCertificate TypeDateItem
G2410265Certificate of AnalysisJun 27, 2024 B108652
G2410264Certificate of AnalysisJun 27, 2024 B108652
G2410217Certificate of AnalysisJun 27, 2024 B108652
I2214315Certificate of AnalysisJun 04, 2024 B108652
I2214314Certificate of AnalysisJun 04, 2024 B108652
C2205215Certificate of AnalysisDec 22, 2023 B108652
F2406034Certificate of AnalysisMay 09, 2023 B108652
F2419062Certificate of AnalysisMay 09, 2023 B108652
C2408172Certificate of AnalysisMay 09, 2023 B108652
H2312023Certificate of AnalysisMay 09, 2023 B108652
H2312025Certificate of AnalysisMay 09, 2023 B108652
H2312042Certificate of AnalysisMay 09, 2023 B108652
H2312362Certificate of AnalysisMay 09, 2023 B108652
L2201605Certificate of AnalysisOct 12, 2022 B108652
L2201602Certificate of AnalysisOct 12, 2022 B108652
L2201606Certificate of AnalysisOct 12, 2022 B108652
L2201607Certificate of AnalysisOct 12, 2022 B108652
L2002099Certificate of AnalysisSep 14, 2022 B108652
I2214363Certificate of AnalysisJun 25, 2022 B108652
I2214313Certificate of AnalysisJun 25, 2022 B108652
C2205178Certificate of AnalysisFeb 10, 2022 B108652
C2205174Certificate of AnalysisFeb 10, 2022 B108652
C2205160Certificate of AnalysisFeb 10, 2022 B108652

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Chemical and Physical Properties

SolubilitySoluble in aqueous alkaline solution, acetic acid, alcohol and acetone. Slightly soluble in carbon tetrachloride. It has poor solubility in water.
Flash Point(°F)440.6 °F
Flash Point(°C)227 °C
Boil Point(°C)220°C
Melt Point(°C)150-155°C

Safety and Hazards(GHS)

Pictogram(s) GHS08,   GHS09,   GHS05,   GHS07
Signal Danger
Hazard Statements

H335:May cause respiratory irritation

H318:Causes serious eye damage

H317:May cause an allergic skin reaction

H360F:May damage fertility

Precautionary Statements

P261:Avoid breathing dust/fume/gas/mist/vapors/spray.

P280:Wear protective gloves/protective clothing/eye protection/face protection.

P302+P352:IF ON SKIN: wash with plenty of water.

P321:Specific treatment (see ... on this label).

P405:Store locked up.

P501:Dispose of contents/container to ...

P271:Use only outdoors or in a well-ventilated area.

P304+P340:IF INHALED: Remove person to fresh air and keep comfortable for breathing.

P403+P233:Store in a well-ventilated place. Keep container tightly closed.

P272:Contaminated work clothing should not be allowed out of the workplace.

P333+P313:IF SKIN irritation or rash occurs: Get medical advice/attention.

P362+P364:Take off contaminated clothing and wash it before reuse.

P203:Obtain, read and follow all safety instructions before use.

P264+P265:Wash hands [and …] thoroughly after handling. Do not touch eyes.

P305+P354+P338:IF IN EYES: Immediately rinse with water for several minutes. Remove contact lenses if present and easy to do. Continue rinsing.

P318:if exposed or concerned, get medical advice.

P317:Get emergency medical help.

P319:Get medical help if you feel unwell.

WGK Germany 2
RTECS SL6300000
Class 9
Merck Index 1297

Related Documents

References

1. Lee HJ, Chattopadhyay S, Gong EY, Ahn RS, Lee K.  (2003)  Antiandrogenic effects of bisphenol A and nonylphenol on the function of androgen receptor..  Toxicol Sci,  75  (1): (40-6).  [PMID:12805653]
2. Yiu KW, Lee CK, Kwok KC, Cheung NH.  (2014)  Measuring the kinetics of the binding of xenoestrogens and estrogen receptor alpha by fluorescence polarization..  Environ Sci Technol,  48  (19): (11591-9).  [PMID:25180905]
3. Zhuang S, Zhang C, Liu W.  (2014)  Atomic Insights into Distinct Hormonal Activities of Bisphenol A Analogues toward PPARγ and ERα Receptors..  Chem Res Toxicol,  27  (10): (1769-79).  [PMID:25233466]

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