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Methylboronic acid (contains varying amounts of Anhydride) - 97%, high purity , CAS No.13061-96-6

3 Citations

COA

Grade & Purity:

≥97%

Cas Number: 13061-96-6
Molecular Weight: 59.86
Beilstein Registry Number: 1731087
MDL number: MFCD00002105
PubChem CID: 139377

In stock

Item Number

M120271

Grouped product items
SKU	Size	Availability	Price
M120271-1g	1g	3	$9.90
M120271-5g	5g	Available within 4-8 weeks(?) Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!	$35.90
M120271-25g	25g	3	$99.90
M120271-100g	100g	2	$299.90
M120271-500g	500g	2	$999.90

View related series

Boron compound (145) Element classified compounds (2014)

Basic Description

Synonyms	Boronic acid, methyl- \| Methylboronic acid \| methyl-boronic acid \| AKOS015915631 \| Dihydroxymethylborane \| M1553 \| KTMKRRPZPWUYKK-UHFFFAOYSA-N \| SB11771 \| STL555616 \| methyboronic acid \| 2-METHYLHYDROGENPYRIDINE-2,5-DICARBOXYLATE \| InChI=1/C18H18O4/c19-17
Specifications & Purity	≥97%
Storage Temp	Store at 2-8°C
Shipped In	Wet ice This product requires cold chain shipping. Ground and other economy services are not available.
Product Description	Reagent used for; 1.Palladium-catalyzed Stille and Suzuki-Miyaura cross-couplings. 2.Microwave-heated heterogeneous Palladium (Pd)-catalytized reactions. 3.Ruthenium (Ru)-catalyzed silylation reactions. 4.Bis(aminotropone) Titanium (Ti) catalysts for ethylene polymerizations. 5.Enantioselective asymmetric bromoaminocyclization and bromoaminocyclization using amino-thiocarbamate catalysts. Reagent used in Preparation of: 1.Common building blocks for pharmaceuticals and agrochemicals. 2.Chrysin analogs by Suzuki-Miyaura coupling reactions. 3.Casein kinase I inhibitors. 4.Divergent C-H functionalizations directed by sulfonamide pharmacophores in drug discovery.

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
- Superclass Organic acids and derivatives
  - Class Boronic acid derivatives
    - Subclass Boronic acids

Kingdom	Organic compounds
Superclass	Organic acids and derivatives
Class	Boronic acid derivatives
Subclass	Boronic acids
Intermediate Tree Nodes	Not available
Direct Parent	Boronic acids
Alternative Parents	Organic metalloid salts Organic oxygen compounds Monoalkylboranes Hydrocarbon derivatives
Molecular Framework	Aliphatic acyclic compounds
Substituents	Boronic acid - Organic metalloid salt - Organic oxygen compound - Monoalkylborane - Alkylborane - Hydrocarbon derivative - Organic salt - Organoboron compound - Aliphatic acyclic compound
Description	This compound belongs to the class of organic compounds known as boronic acids. These are compounds comprising the boronic acid functional group RB(O)O (R,R'=alkyl, aryl).
External Descriptors	Not available
1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61. DOI: 10.1186/s13321-016-0174-y

Associated Targets(Human)

TRPV6 Tchem Transient receptor potential cation channel subfamily V member 6 (136 Activities)

Discover Target: TRPV6

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Mechanisms of Action

Mechanism of Action	Action Type	target ID	Target Name	Target Type	Target Organism	Binding Site Name	References

Names and Identifiers

IUPAC Name	methylboronic acid
INCHI	InChI=1S/CH5BO2/c1-2(3)4/h3-4H,1H3
InChIKey	KTMKRRPZPWUYKK-UHFFFAOYSA-N
Smiles	B(C)(O)O
Isomeric SMILES	B(C)(O)O
WGK Germany	3
Molecular Weight	59.86
Beilstein	1731087
Reaxy-Rn	1731087
Reaxys-RN_link_address	https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1731087&ln=

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.

20 results found

Lot Number	Certificate Type	Date	Item
L1726057	Certificate of Analysis	Jul 09, 2025	M120271
F2505459	Certificate of Analysis	May 21, 2025	M120271
F2505460	Certificate of Analysis	May 21, 2025	M120271
F2505478	Certificate of Analysis	May 21, 2025	M120271
B2511235	Certificate of Analysis	Jan 16, 2025	M120271
B2511298	Certificate of Analysis	Jan 16, 2025	M120271
G2416234	Certificate of Analysis	Apr 29, 2024	M120271
G2416235	Certificate of Analysis	Apr 29, 2024	M120271
G2415773	Certificate of Analysis	Apr 29, 2024	M120271
L2413067	Certificate of Analysis	Aug 18, 2023	M120271
H2330592	Certificate of Analysis	Aug 18, 2023	M120271
H2330593	Certificate of Analysis	Aug 18, 2023	M120271
H2330594	Certificate of Analysis	Aug 18, 2023	M120271
H2330595	Certificate of Analysis	Aug 18, 2023	M120271
D1910032	Certificate of Analysis	Feb 03, 2023	M120271
C1905121	Certificate of Analysis	Dec 12, 2022	M120271
C1905120	Certificate of Analysis	Dec 12, 2022	M120271
K1710013	Certificate of Analysis	Dec 12, 2022	M120271
E2217149	Certificate of Analysis	Mar 09, 2022	M120271
E2217146	Certificate of Analysis	Mar 09, 2022	M120271

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Chemical and Physical Properties

Solubility	Soluble in water.
Sensitivity	Hygroscopic；Heat sensitive
Melt Point(°C)	91°C
Molecular Weight	59.860 g/mol
XLogP3
Hydrogen Bond Donor Count	2
Hydrogen Bond Acceptor Count	2
Rotatable Bond Count	0
Exact Mass	60.0383 Da
Monoisotopic Mass	60.0383 Da
Topological Polar Surface Area	40.500 Å²
Heavy Atom Count	4
Formal Charge	0
Complexity	13.500
Isotope Atom Count	0
Defined Atom Stereocenter Count	0
Undefined Atom Stereocenter Count	0
Defined Bond Stereocenter Count	0
Undefined Bond Stereocenter Count	0
The total count of all stereochemical bonds	0
Covalently-Bonded Unit Count	1

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