4,4,5,5-Tetramethyl-1,3,2-dioxaborolane - ≥97% , CAS No.25015-63-8

CAS: 25015-63-8 Cat. No.: T113748 Molecular Weight: 127.98 EC Number: 607-485-3 PubChem CID: 6364989
AVAILABLE TO ORDER
GRADE & PURITY ≥97%
Synonyms
EC 607-485-3 | boronic acid pinacol ester | 4,4,5,5-Tetramethyl-1,3,2-dioxaborolane | 4,4,5,5-tetramethyl-1,3,2-dioxa-borolane | T2572 | DTXSID30422852 | EN300-73933 | SCHEMBL80492 | 4,4,5,5-tetramethyl-1,3,2$l^{2} | Pinacolborane, 1.0M in THF | AS-40957
Storage
Store at 2-8°C,Argon charged
Shipped In
Wet ice
 ·  off list, applied to all prices below.
Size
Status
Price
Qty
5ml
T113748-5ml
2
$9.90
25ml
T113748-25ml
3
$25.90
100ml
T113748-100ml
1
$94.90
500ml
T113748-500ml
8-12 wks(?) Production requires sourcing of materials. We appreciate your patience and understanding.
$377.90
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

Store at 2-8°C,Argon charged Ships Wet ice Check lot-specific COA for exact specifications.

📋

Quality documents

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

📚

Literature proof

Cited in 1 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Specifications

Synonyms
EC 607-485-3 | boronic acid pinacol ester | 4, 4, 5, 5-Tetramethyl-1, 3, 2-dioxaborolane | 4, 4, 5, 5-tetramethyl-1, 3, 2-dioxa-borolane | T2572 | DTXSID30422852 | EN300-73933 | SCHEMBL80492 | 4, 4, 5, 5-tetramethyl-1, 3, 2$l^{2} | Pinacolborane, 1.0M in THF | AS-40957
Specifications & Purity
≥97%
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
≥97%
Names and Identifiers
Canonical Smiles[B]1OC(C(O1)(C)C)(C)C
InChIKeyLZPWAYBEOJRFAX-UHFFFAOYSA-N
INCHI1S/C6H12BO2/c1-5(2)6(3,4)9-7-8-5/h1-4H3
Isomeric SMILES [B]1OC(C(O1)(C)C)(C)C
WGK Germany 3
PubChem CID 6364989
UN Number 3398
Molecular Weight 127.98
Reaxy-Rn 7802871

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.

25 results found

Lot NumberCertificate TypeDateItem
L2529262Certificate of AnalysisDec 16, 2025 T113748
L2529247Certificate of AnalysisDec 16, 2025 T113748
L2529244Certificate of AnalysisDec 16, 2025 T113748
D2616103Certificate of AnalysisDec 16, 2025 T113748
K2517232Certificate of AnalysisJul 03, 2025 T113748
G2516563Certificate of AnalysisJul 03, 2025 T113748
G2516562Certificate of AnalysisJul 03, 2025 T113748
G2516371Certificate of AnalysisJul 03, 2025 T113748
G2516561Certificate of AnalysisJul 03, 2025 T113748
B2526279Certificate of AnalysisJan 22, 2025 T113748
G2504034Certificate of AnalysisJan 22, 2025 T113748
B2526296Certificate of AnalysisJan 22, 2025 T113748
B2526282Certificate of AnalysisJan 22, 2025 T113748
G2522114Certificate of AnalysisApr 11, 2024 T113748
H2412357Certificate of AnalysisApr 11, 2024 T113748
H2412358Certificate of AnalysisApr 11, 2024 T113748
H2412470Certificate of AnalysisApr 11, 2024 T113748
A2506190Certificate of AnalysisApr 11, 2024 T113748
I2313422Certificate of AnalysisAug 29, 2023 T113748
I2313423Certificate of AnalysisAug 29, 2023 T113748
I2313455Certificate of AnalysisAug 29, 2023 T113748
J2429064Certificate of AnalysisAug 29, 2023 T113748
E2323020Certificate of AnalysisMay 28, 2022 T113748
I2212401Certificate of AnalysisMay 28, 2022 T113748
E2112253Certificate of AnalysisMay 22, 2021 T113748

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Chemical and Physical Properties
SensitivityMoisture sensitive;Air sensitive;heat sensitive
Refractive Index1.394-1.396
Flash Point(°F)5℃
Flash Point(°C)5℃
Boil Point(°C)43 °C/50 mmHg
Molecular Weight126.970 g/mol
XLogP3
Hydrogen Bond Donor Count0
Hydrogen Bond Acceptor Count2
Rotatable Bond Count0
Exact Mass127.093 Da
Monoisotopic Mass127.093 Da
Topological Polar Surface Area18.500 Ų
Heavy Atom Count9
Formal Charge0
Complexity106.000
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
Pinacolborane
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)
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)
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
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
1. Zhiyuan Li, Yanan Dai, Lishuang Shi, Weihao Wu, Hongyan Xie, Zehuai Mou.  (2025)  Trifluoromethyl-Containing β-Diketiminato-Magnesium Complexes: Synthesis, Structures, and Catalysis for the Hydroboration of Carbodiimides.  APPLIED ORGANOMETALLIC CHEMISTRY,  39  (6): (e70185).  [PMID:] [10.1002/aoc.70185]
Solution Calculators
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