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2,6-Lutidine-α2,3-diol - 99%, high purity , CAS No.42097-42-7

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2,6-Lutidine-α2,3-diol - 99%, high purity , CAS No.42097-42-7

COA

Grade & Purity:

≥99%

Cas Number: 42097-42-7
Molecular Weight: 139.15
PubChem CID: 135128
PubChem SID: 488187831

In stock

Item Number

L170275

Grouped product items
SKU	Size	Availability	Price
L170275-1g	1g	3	$34.90
L170275-5g	5g	3	$155.90
L170275-10g	10g	1	$205.90
L170275-25g	25g	Available within 4-8 weeks(?) Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!	$461.90
L170275-100g	100g	Available within 4-8 weeks(?) Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!	$1,662.90

Basic Description

Synonyms	2-(hydroxymethyl)-6-methylpyridin-3-ol \| 42097-42-7 \| 3-Hydroxy-6-methyl-2-pyridinemethanol \| 3-Hydroxy-2-hydroxymethyl-6-methylpyridine \| 2-Pyridinemethanol, 3-hydroxy-6-methyl- \| 53GWV75WPC \| 2-Hydroxymethyl-6-methyl-pyridin-3-ol \| EINECS 255-657-8 \| 3-Hydroxy-6-methyl
Specifications & Purity	≥99%
Storage Temp	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.
Product Description	Product description： 2,6-Lutidine-α2,3-diol (3-Hydroxy-6-methyl-2-pyridinemethanol) on condensation with chlorides of carbamidophosphoric acids yields N-Substituted N′-[6-methyl-2-oxido-1,3,2-dioxaphosphinino(5,4,-b)pyridine-2-yl]urea. It forms organotin (IV) complexes on reaction with dimethyl-, diethyl- and dibutyltin (IV) oxide. Application： 2,6-Lutidine-α2,3-diol (3-Hydroxy-6-methyl-2-pyridinemethanol) was used in the synthesis of: (3-hydroxy-6-methylpyridin-2-yl)methyl pivaloate triflate (3-(allyloxy)-6-methylpyridin-2-yl)methanol

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
- Superclass Organoheterocyclic compounds
  - Class Pyridines and derivatives
    - Subclass Methylpyridines

Kingdom	Organic compounds
Superclass	Organoheterocyclic compounds
Class	Pyridines and derivatives
Subclass	Methylpyridines
Intermediate Tree Nodes	Not available
Direct Parent	Methylpyridines
Alternative Parents	Hydroxypyridines Heteroaromatic compounds Azacyclic compounds Primary alcohols Organopnictogen compounds Organonitrogen compounds Hydrocarbon derivatives Aromatic alcohols
Molecular Framework	Aromatic heteromonocyclic compounds
Substituents	Methylpyridine - Hydroxypyridine - Heteroaromatic compound - Azacycle - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Hydrocarbon derivative - Aromatic alcohol - Primary alcohol - Organooxygen compound - Organonitrogen compound - Alcohol - Aromatic heteromonocyclic compound
Description	This compound belongs to the class of organic compounds known as methylpyridines. These are organic compounds containing a pyridine ring substituted at one or more positions by a methyl group.
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)

ALDH1A1 Tchem Aldehyde dehydrogenase 1A1 (77053 Activities)

Discover Target: ALDH1A1

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

GLP1R Tclin Glucagon-like peptide 1 receptor (111429 Activities)

Discover Target: GLP1R

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

Associated Targets(non-human)

Plasmodium falciparum (966862 Activities)

Explore this target

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

Pubchem Sid	488187831
Pubchem Sid Url	https://pubchem.ncbi.nlm.nih.gov/substance/488187831
IUPAC Name	2-(hydroxymethyl)-6-methylpyridin-3-ol
INCHI	InChI=1S/C7H9NO2/c1-5-2-3-7(10)6(4-9)8-5/h2-3,9-10H,4H2,1H3
InChIKey	PAGTXDLKXRBHFL-UHFFFAOYSA-N
Smiles	CC1=NC(=C(C=C1)O)CO
Isomeric SMILES	CC1=NC(=C(C=C1)O)CO
WGK Germany	3
Molecular Weight	139.15
Reaxy-Rn	120696
Reaxys-RN_link_address	https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=120696&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.

8 results found

Lot Number	Certificate Type	Date	Item
C2318014	Certificate of Analysis	Jan 07, 2023	L170275
C23171035	Certificate of Analysis	Jan 07, 2023	L170275
C2317916	Certificate of Analysis	Jan 07, 2023	L170275
C2317919	Certificate of Analysis	Jan 07, 2023	L170275
C2317981	Certificate of Analysis	Jan 07, 2023	L170275
C2318004	Certificate of Analysis	Jan 07, 2023	L170275
C2317850	Certificate of Analysis	Jan 07, 2023	L170275
C23171042	Certificate of Analysis	Jan 07, 2023	L170275

Chemical and Physical Properties

Molecular Weight	139.150 g/mol
XLogP3	0.600
Hydrogen Bond Donor Count	2
Hydrogen Bond Acceptor Count	3
Rotatable Bond Count	1
Exact Mass	139.063 Da
Monoisotopic Mass	139.063 Da
Topological Polar Surface Area	53.400 Å²
Heavy Atom Count	10
Formal Charge	0
Complexity	108.000
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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