Phenylboronic acid (PBA)(contains varying amounts of Anhydride) - ≥97% , CAS No.98-80-6

CAS: 98-80-6 Cat. No.: P107045 Peso molecular: 121.93 Beilstein Registry Number: 970972 Número EC: 202-701-9
Disponible para pedir
GRADE & PURITY ≥97%
Synonyms
Phenyldihydroxyborane | Borophenylic acid | Dihydroxy(phenyl)borane | Phenylboronic acid | Benzeneboronic acid | Dihydroxyphenylborane | USAF BO-2 | NSC 66487
Storage
Room temperature,Argon charged
Shipped In
Normal
 ·  off list, applied to all prices below.
Size
Estado
Price
Qty
5g
P107045-5g
2
9,90US$
25g
P107045-25g
3

17,90US$

26,90US$
Guardar 9,00 US$ (33.46%)
50g
P107045-50g
2
29,90US$
100g
P107045-100g
2
47,90US$
250g
P107045-250g
2
99,90US$
Enter a quantity for the sizes you want to add.
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Why this grade

≥97% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Room temperature,Argon charged Ships Normal Check lot-specific COA for exact specifications.

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Quality documents

SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.

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Literature proof

Cited in 103 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Descripción general

Phenylboronic acid is a highly stable receptor ligand used in cross-coupling reactions and drug delivery. Phenylboronic acid (PBA) is an organoboronic acid. It behaves as a molecular receptor that can attach to compounds containing cis-diol group. Microwave-assisted Suzuki coupling of aryl chlorides with phenylboronic acid in the presence of Pd/C (catalyst) and water (solvent) has been described.Palladium-catalyzed cross-coupling reaction of phenylboronicacid with haloarenes to afford biaryls has been reported.

Specifications

Sinónimos
Phenyldihydroxyborane | Borophenylic acid | Dihydroxy(phenyl)borane | Phenylboronic acid | Benzeneboronic acid | Dihydroxyphenylborane | USAF BO-2 | NSC 66487
Especificaciones y pureza
≥97%
Condiciones de almacenamiento de almacenamiento
Room temperature, Argon charged
Enviado en
Normal
Pureza
≥97%
Nombres e identificadores
Sonrisas canónicasB(C1=CC=CC=C1)(O)O
IUPAC Namephenylboronic acid
InChIKeyHXITXNWTGFUOAU-UHFFFAOYSA-N
INCHI1S/C6H7BO2/c8-7(9)6-4-2-1-3-5-6/h1-5,8-9H
Isómeros SMILES B(C1=CC=CC=C1)(O)O
WGK Alemania 3
RTECS CY8575000
Peso molecular 121.93
Beilstein 970972
Reaxy-Rn 970972
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=970972&ln=

Documentation

📋 Safety Data Sheet (SDS)

Comprehensive hazard, handling, storage, and regulatory compliance document.

Download SDS →

✅ Certificate of Analysis (COA)

Lot-specific quality data. Enter your lot number to retrieve the exact COA.

Look up COA →

📊 Datasheet

Quick-reference summary of product specifications and applications.

View datasheet →

🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

View spec sheet →

Advanced Data

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassBenzenoids
ClaseBenzene and substituted derivatives
SubclassNot available
Intermediate Tree Nodes Not available
Direct ParentBenzene and substituted derivatives
Alternative Parents Boronic acids  Organic metalloid salts  Organoboron compounds  Organic oxygen compounds  Hydrocarbon derivatives  
Molecular FrameworkAromatic homomonocyclic compounds
Substituents Monocyclic benzene moiety - Boronic acid - Boronic acid derivative - Organic metalloid salt - Organic oxygen compound - Hydrocarbon derivative - Organic salt - Organoboron compound - Aromatic homomonocyclic compound
DescripciónThis compound belongs to the class of organic compounds known as benzene and substituted derivatives. These are aromatic compounds containing one monocyclic ring system consisting of benzene.
External Descriptors boronic acids
Estructura 3D
Modelo de Estructura Química Interactiva





Objetivos asociados (humanos)
CA6 Tclin Carbonic anhydrase 6 (1 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
CA4 Tclin Carbonic anhydrase 4 (3 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
CA2 Tclin Carbonic anhydrase II (17698 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
PRSS1 Tclin Trypsin I (2306 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ACHE Tclin Acetylcholinesterase (18204 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CA3 Tclin Carbonic anhydrase III (753 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CA6 Tclin Carbonic anhydrase VI (993 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CA1 Tclin Carbonic anhydrase I (13240 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CA5B Tclin Carbonic anhydrase VB (957 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CA5A Tclin Carbonic anhydrase VA (1168 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CA14 Tclin Carbonic anhydrase XIV (1305 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CA12 Tclin Carbonic anhydrase XII (6231 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
PCSK9 Tclin Subtilisin/kexin type 9 (362 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CA9 Tclin Carbonic anhydrase IX (8255 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SH-SY5Y (11521 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
MGLL Tchem Monoglyceride lipase (1909 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ENPP2 Tchem Autotaxin (2645 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
TRPV6 Tchem Transient receptor potential cation channel subfamily V member 6 (136 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CA5B Tclin Carbonic anhydrase V (54 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ORAI1 Tchem ORAI 1/2/3 (82 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Objetivos asociados (no humanos)
bla Beta-lactamase TEM (457 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
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Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Alpha-chymotrypsin (819 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Ca7 Carbonic anhydrase VII (3 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Ca13 Carbonic anhydrase XIII (322 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CA4 Carbonic anhydrase IV (1713 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Faah Anandamide amidohydrolase (3907 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Carbonic anhydrase (69 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Staphylococcus aureus (210822 Activities)
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Trypanosoma cruzi (99888 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Subtilisin (36 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
norA Quinolone resistance protein norA (2171 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
rep Replicase polyprotein 1ab (378 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
blaKPC-2 Class A carbapenemase KPC-2 (126 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Ca15 Carbonic anhydrase 15 (173 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
mtcA1 Uncharacterized protein Rv1284/MT1322 (182 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
dac D-alanyl-D-alanine carboxypeptidase (132 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
pbpX Penicillin-binding protein 2x (156 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CA Alpha carbonic anhydrase (93 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
dapE Succinyl-diaminopimelate desuccinylase (42 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Astrosclerin-3 (80 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mecanismos de acción
Certificados (CoA, COO, BSE/TSE y tabla de análisis)
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.

32 results found

Lot NumberCertificate TypeFechaArticulo
I2202671Certificate of AnalysisJun 11, 2026 P107045
I2202663Certificate of AnalysisJun 11, 2026 P107045
D2623409Certificate of AnalysisApr 13, 2026 P107045
D2623406Certificate of AnalysisApr 13, 2026 P107045
D2623407Certificate of AnalysisApr 13, 2026 P107045
D2623408Certificate of AnalysisApr 13, 2026 P107045
A2203351Certificate of AnalysisOct 13, 2025 P107045
E2515473Certificate of AnalysisApr 27, 2025 P107045
E2520699Certificate of AnalysisApr 27, 2025 P107045
E2515504Certificate of AnalysisApr 27, 2025 P107045
C2611182Certificate of AnalysisApr 27, 2025 P107045
F2523192Certificate of AnalysisOct 16, 2024 P107045
J2430477Certificate of AnalysisOct 16, 2024 P107045
J2430478Certificate of AnalysisOct 16, 2024 P107045
J2430467Certificate of AnalysisOct 16, 2024 P107045
D2530252Certificate of AnalysisAug 17, 2024 P107045
D2508726Certificate of AnalysisAug 17, 2024 P107045
F2412325Certificate of AnalysisMay 27, 2024 P107045
F2412326Certificate of AnalysisMay 27, 2024 P107045
F2412327Certificate of AnalysisMay 27, 2024 P107045
H2401062Certificate of AnalysisMay 27, 2024 P107045
K1929044Certificate of AnalysisSep 12, 2023 P107045
J2308542Certificate of AnalysisSep 06, 2023 P107045
J2308543Certificate of AnalysisSep 06, 2023 P107045
J2308544Certificate of AnalysisSep 06, 2023 P107045
A2408020Certificate of AnalysisSep 06, 2023 P107045
K1520035Certificate of AnalysisJul 31, 2023 P107045
I2202772Certificate of AnalysisJul 19, 2022 P107045
I2202773Certificate of AnalysisJul 19, 2022 P107045
I2202769Certificate of AnalysisJul 19, 2022 P107045
B2323551Certificate of AnalysisJul 19, 2022 P107045
B2307212Certificate of AnalysisJul 19, 2022 P107045

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Propiedades químicas y físicas
SolubilidadSoluble in water (10 mg/ml at 20 °C), ether (30.2%), chloroform, methanol (178%), and DMSO.
SensibilidadHygroscopic
Punto de fusión (°C)217-220°C
Peso molecular121.930 g/mol
XLogP3
Hydrogen Bond Donor Count2
Hydrogen Bond Acceptor Count2
Rotatable Bond Count1
Exact Mass122.054 Da
Monoisotopic Mass122.054 Da
Topological Polar Surface Area40.500 Ų
Heavy Atom Count9
Formal Charge0
Complexity79.100
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count1
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Citations of This Product
Referencias
1. Yan Zhu, Shaochen Sun, Hongye Li, Liuqi Kong, Yuhang Xu, Farong Tao, Liping Wang, Guang Li.  (2023)  Achieving color-tunable persistent afterglow from ultralong polyacrylamide-based room-temperature phosphorescence materials through phosphorescence Förster resonance energy transfer.  EUROPEAN POLYMER JOURNAL,      [PMID:] [10.1016/j.eurpolymj.2023.112600]
2. Rui Zhu, Wenhua Du, Xiaohui Mi.  (2023)  Injectable, pH-responsive hybrid hydrogels for the treatment of periodontitis.  CELLULAR AND MOLECULAR BIOLOGY,  69  (15): (210-216).  [PMID:38279440] [10.14715/cmb/2023.69.15.36]
3. JunHui Hu, Ying Yan, Huiping Zhang.  (2023)  Preparation of a new B-CNTs/PSSF composite catalyst for catalytic wet peroxide oxidation of phenol in structured fixed bed.  Journal of Environmental Chemical Engineering,      [PMID:] [10.1016/j.jece.2023.111704]
4. Rongxiu Qin, Haiyan Chen, Rusi Wen, Guiqing Li, Zhonglei Meng.  (2023)  Effect of Boric Acid on the Ionization Equilibrium of α-Hydroxy Carboxylic Acids and the Study of Its Applications.  MOLECULES,  28  (12): (4723).  [PMID:37375278] [10.3390/molecules28124723]
5. Yanli Li, Yanmei Si, Genmei Yang, Lixia Yang, Hua Wang.  (2023)  Rational design of a functionalized metal–organic framework for ratiometric fluorimetric sensing of Hg2+ in environmental water.  Analytical Methods,  15  (21): (2599-2605).  [PMID:37226573] [10.1039/D3AY00546A]
6. Xiaojing Lv, Xuchen Zhu, Ling Zhang, Mi Ouyang, Minao Xia, Chunyan Liu, Cheng Zhang.  (2023)  Highly transparent to red/green/blue photo-crosslinkable polymer for patterned electrochromic device.  Journal of Materials Chemistry C,  11  (16): (5490-5497).  [PMID:] [10.1039/D3TC00325F]
7. Wenqi Jiang, Mingkang Liang, Qifang Lei, Dashi Deng, Chenchen Li, Yuqing Li, Simin Yuan, Kai Wu, Guangzhi Li, Song Wu.  (2023)  Phenylboronic acid-functionalized chitosan for enabling transmucosal delivery for cancer therapy.  MATERIALS & DESIGN,      [PMID:] [10.1016/j.matdes.2023.111843]
8. Wenhui Wang, Kaijin Chen, Huiyan Wu, Yubo Long, Juan Zhao, Long Jiang, Siwei Liu, Zhenguo Chi, Jiarui Xu, Yi Zhang.  (2023)  Benzoxazole-Based Hybridized Local and Charge-Transfer Deep-Blue Emitters for Solution-Processable Organic Light-Emitting Diodes and the In fluences of Hexahydrophthalimido.  ACS Applied Materials & Interfaces,      [PMID:36867671] [10.1021/acsami.2c23254]
9. Qiyu Meng, Meng Rong, Huifang Xing, Jiemiao Yu, Yupei Wang, Xuetuan Wei, Ru-An Chi, Congmei Chen, Huizhou Liu, Liangrong Yang.  (2023)  One-step synthesis of boronic acid-functionalized hypercrosslinked polymers for efficient separation of 1,2,4-butanetriol.  SEPARATION AND PURIFICATION TECHNOLOGY,      [PMID:] [10.1016/j.seppur.2023.123436]
10. Liqun Zhang, Pinggu Wu, Xiaoling Xiang, Huali He, Sha Yu.  (2023)  Risk assessment of 3-monochloropropane-1,2-diol esters through dietary exposure from edible oils for the Zhejiang population in China by Monte Carlo simulation.  Food Additives and Contaminants Part A-Chemistry Analysis Control Exposure & Risk Assessment,      [PMID:36512554] [10.1080/19440049.2022.2155709]
11. Lihuang Wu, Yuqi Wang, Xinyue Zhao, Hongli Mao, Zhongwei Gu.  (2023)  Investigating the Biodegradation Mechanism of Poly(trimethylene carbonate): Macrophage-Mediated Erosion by Secreting Lipase.  BIOMACROMOLECULES,      [PMID:36644840] [10.1021/acs.biomac.2c01350]
12. Liuqi Kong, Yan Zhu, Shaochen Sun, Hongye Li, Farong Tao, Fei Li, Liping Wang, Guang Li.  (2023)  Color-tunable and ultralong organic room temperature phosphorescence from poly(acrylic acid)-based materials through hydrogen bond engineering.  Journal of Materials Chemistry C,  11  (5): (1960-1970).  [PMID:] [10.1039/D2TC04789F]
13. Yingrui Ji, Dongming Lan, Weifei Wang, Kok Ming Goh, Chin Ping Tan, Yonghua Wang.  (2022)  The Formation of 3-Monochloropropanediol Esters and Glycidyl Esters during Heat-Induced Processing Using an Olive-Based Edible Oil.  Foods,  11  (24): (4073).  [PMID:36553815] [10.3390/foods11244073]
14. Lili Long, Yuelong Liu, Wei Liu.  (2022)  Boric acid as a hydrogen bond donor with TBAB catalyze the cycloaddition of CO2 to internal bio-epoxides under solvent-free conditions.  Molecular Catalysis,      [PMID:] [10.1016/j.mcat.2022.112849]
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23. Zhe Zheng, Mingwu Qiao, Zhongwei Zhang, Chang Li.  (2021)  Phytosterols inhibit the formation of 3-monochloropropane-1,2-diol esters in model reactions and the possible mechanism.  FOOD SCIENCE AND TECHNOLOGY RESEARCH,      [PMID:] [10.3136/fstr.27.789]
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28. Qiyu Meng, Jiemiao Yu, Liangrong Yang, Yanqing Li, Mo Xian, Huizhou Liu.  (2020)  Efficient recovery of bio-based 1,2,4-butanetriol by using boronic acid anionic reactive extraction.  SEPARATION AND PURIFICATION TECHNOLOGY,      [PMID:] [10.1016/j.seppur.2020.117728]
29. Benben Zhang, Zeyu Ye, Min Qin, Qingqing Wang, Yijun Du, Chenze Qi, Linjun Shao.  (2020)  Palladium complex embedded crosslinked polystyrene nanofibers as a green and efficient heterogeneous catalyst for coupling reactions.  JOURNAL OF APPLIED POLYMER SCIENCE,  138  (2): (49666).  [PMID:] [10.1002/app.49666]
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