Bis(pinacolato)diboron - ≥98% , CAS No.73183-34-3

CAS: 73183-34-3 Cat. No.: B106765 Molecular Weight: 253.94 EC Number: 615-925-0
AVAILABLE TO ORDER
GRADE & PURITY ≥98%
Synonyms
4,4,5,5,4',4',5',5'-octamethyl-[2,2']bi[1,3,2]dioxaborolanyl | bis (pinacolato) diborane | Dipinacoldiboron | dipinacol-diboron | MFCD00799570 | UNII-I906W26P4U | B2Pin2 | Bis(2,2,3,3-tetramethyl-2,3-butanedionato)diboron | bis(pinacolate)diborane(4) | DT
Storage
Store at 2-8°C,Argon charged
Shipped In
Wet ice
 ·  off list, applied to all prices below.
Size
Status
Price
Qty
1g
B106765-1g
10
$9.90
5g
B106765-5g
8
$10.90
10g
B106765-10g
1
$12.90
25g
B106765-25g
≥10
$14.90
100g
B106765-100g
≥10

$31.90

$47.90
Save $16.00 (33.40%)
500g
B106765-500g
1
$142.90
Enter a quantity for the sizes you want to add.
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Why this grade

≥98% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

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Storage & shipping

Store at 2-8°C,Argon charged Ships Wet ice 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 29 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Overview

Bis(pinacolato)diboron is used to construct a tetramethylpyrrolidine nitroxide scaffold for the synthesis of paramagnetic heterocycles by Suzuki coupling. It is also a substrate used in new palladium-catalyzed cyclization of 1,6-enynes leading to homoallylic alkylboronates.
A reagent used for the cis-vicinal diborylation of acetylenes and olefins with Pt catalysis; borylation of aromatics by Pd catalysis

Specifications

Synonyms
4, 4, 5, 5, 4', 4', 5', 5'-octamethyl-[2, 2']bi[1, 3, 2]dioxaborolanyl | bis (pinacolato) diborane | Dipinacoldiboron | dipinacol-diboron | MFCD00799570 | UNII-I906W26P4U | B2Pin2 | Bis(2, 2, 3, 3-tetramethyl-2, 3-butanedionato)diboron | bis(pinacolate)diborane(4) | DT
Specifications & Purity
≥98%
Storage
Store at 2-8°C, Argon charged
Shipped In
Wet ice
This product requires cold chain shipping. Ground and other economy services are not available.
Purity
≥98%
Names and Identifiers
Pubchem Sid488192410
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/488192410
Canonical SmilesB1(OC(C(O1)(C)C)(C)C)B2OC(C(O2)(C)C)(C)C
IUPAC Name4,4,5,5-tetramethyl-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1,3,2-dioxaborolane
InChIKeyIPWKHHSGDUIRAH-UHFFFAOYSA-N
INCHI1S/C12H24B2O4/c1-9(2)10(3,4)16-13(15-9)14-17-11(5,6)12(7,8)18-14/h1-8H3
Isomeric SMILES B1(OC(C(O1)(C)C)(C)C)B2OC(C(O2)(C)C)(C)C
WGK Germany 3
Molecular Weight 253.94
Reaxy-Rn 7703552
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=7703552&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
SuperclassOrganoheterocyclic compounds
ClassDioxaborolanes
SubclassNot available
Intermediate Tree Nodes Not available
Direct ParentDioxaborolanes
Alternative Parents Oxacyclic compounds  Organic metalloid salts  Organooxygen compounds  Hydrocarbon derivatives  
Molecular FrameworkAliphatic heteromonocyclic compounds
Substituents 1,3,2-dioxaborolane - Oxacycle - Organic metalloid salt - Organic oxygen compound - Hydrocarbon derivative - Organic salt - Organooxygen compound - Aliphatic heteromonocyclic compound
DescriptionThis compound belongs to the class of organic compounds known as dioxaborolanes. These are compounds containing a five-member saturated aliphatic heterocycle made up of two oxygen atoms, a boron atom, and three carbon atoms.
External Descriptors Not available
3D Structure
Interactive Chemical Structure Model





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.

39 results found

Lot NumberCertificate TypeDateItem
C2623534Certificate of AnalysisMar 09, 2026 B106765
C2623533Certificate of AnalysisMar 09, 2026 B106765
C2623532Certificate of AnalysisMar 09, 2026 B106765
C2623531Certificate of AnalysisMar 09, 2026 B106765
C2623530Certificate of AnalysisMar 09, 2026 B106765
C2623529Certificate of AnalysisMar 09, 2026 B106765
C2623528Certificate of AnalysisMar 09, 2026 B106765
G2516099Certificate of AnalysisJun 21, 2025 B106765
G2516100Certificate of AnalysisJun 21, 2025 B106765
G2516101Certificate of AnalysisJun 21, 2025 B106765
G2516102Certificate of AnalysisJun 21, 2025 B106765
G2516103Certificate of AnalysisJun 21, 2025 B106765
H2120161Certificate of AnalysisJun 10, 2025 B106765
H2120162Certificate of AnalysisJun 10, 2025 B106765
H2120163Certificate of AnalysisJun 10, 2025 B106765
B2103144Certificate of AnalysisDec 16, 2024 B106765
D2423153Certificate of AnalysisMar 25, 2024 B106765
H2408143Certificate of AnalysisMar 25, 2024 B106765
D2423152Certificate of AnalysisMar 25, 2024 B106765
D2420095Certificate of AnalysisMar 25, 2024 B106765
F2419116Certificate of AnalysisMar 25, 2024 B106765
E2509214Certificate of AnalysisMar 25, 2024 B106765
H2419099Certificate of AnalysisNov 05, 2022 B106765
A2506281Certificate of AnalysisNov 05, 2022 B106765
K2507026Certificate of AnalysisNov 05, 2022 B106765
E2517018Certificate of AnalysisNov 05, 2022 B106765
B2321162Certificate of AnalysisNov 05, 2022 B106765
B2321153Certificate of AnalysisNov 05, 2022 B106765
B2321140Certificate of AnalysisNov 05, 2022 B106765
B2321139Certificate of AnalysisNov 05, 2022 B106765
B2321125Certificate of AnalysisNov 05, 2022 B106765
B2321112Certificate of AnalysisNov 05, 2022 B106765
B2321104Certificate of AnalysisNov 05, 2022 B106765
G1418028Certificate of AnalysisApr 27, 2022 B106765
B2225620Certificate of AnalysisMar 05, 2022 B106765
G2307544Certificate of AnalysisAug 06, 2021 B106765
E2417077Certificate of AnalysisAug 06, 2021 B106765
D2403010Certificate of AnalysisAug 06, 2021 B106765
B2103142Certificate of AnalysisMar 05, 2021 B106765

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Chemical and Physical Properties
SolubilitySoluble in tetrahydrofuran, dichloromethane, toluene, hexane and heptane. Insoluble in water.
SensitivityMoisture & heat sensitive
Melt Point(°C)135-140°C
Molecular Weight253.900 g/mol
XLogP3
Hydrogen Bond Donor Count0
Hydrogen Bond Acceptor Count4
Rotatable Bond Count1
Exact Mass254.186 Da
Monoisotopic Mass254.186 Da
Topological Polar Surface Area36.900 Ų
Heavy Atom Count18
Formal Charge0
Complexity286.000
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
Documents & Articles
9-Borabicyclo[3.3.1]nonane / 9-BBN
Bis(pinacolato)diboron, B2pin2
Diphenylsilane
Hydrogen peroxide
One Atom Can Change a Drug’s Fate: Atom-Level Knobs and a Functional-Group Toolbox for Medicinal Chemistry (Methyl / Halogen Bonding / 3D Building Blocks / Late-Stage Fluorination + Product-Selection Tables)
Strategies and Progress in the Asymmetric Catalytic Synthesis of Chiral 1,2-Bis(boronic) Esters: Route Types, Selectivity Challenges, and Sequential Site Utilization (with Product Selection Navigator and Tables 1–4)
From Piperidine to Pyridine: The “Most Common N-Heterocycle” Shift in FDA Small-Molecule New Drugs (2013–2023) and a Selection Guide (Tables 1–4)
Make “Aryl Chlorides + Low Pd Loading + Scale-Up Reproducibility” Reliable: The Initiation and Durability Logic of Pd–NHC (Palladium–N-Heterocyclic Carbene) Cross-Coupling (with Selection Navigation and Product Tables)
Choosing Boron Sources to Make Reactions Robust: How Boronic Acids, Boronate Esters, BF₃K Salts, and MIDA Improve Suzuki–Miyaura Start-Up and Scale-Up Reproducibility (with Product Tables 1–5)
How to Make the Suzuki–Miyaura Reaction Robust: Pinpoint the Bottleneck and Lock in a Reproducible Operating Window (with Selection Navigation and Product Tables 1–5)
Haloheterocycles and Cross-Coupling: A Research-Oriented Selection Framework from Substrate Identification to Bond-Forming Routes (Including Product Navigation and Tables 1–5)
Experimental Selection Logic for C-C Bond Construction: Understanding Fragment Coupling, Carbonyl Chain Extension, Olefination, and Late-Stage Bond-Forming Pathways by Bond-Forming Task
Reaction Selection in Small-Molecule Synthesis: From Transformation-Type Assessment to Experimental Route Screening
Experimental Selection Logic for Transition-Metal-Catalyzed C–H Functionalization: When It Is Worth Pursuing and How to Assess Site Selectivity and Conditions
Experimental Decision-Making for Cross-Coupling Reactions: Target Bond Type, Substrate Combination, and Catalytic System Selection
Citations of This Product
References
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