1-(6-(tert-Butylamino)-4-methylpyridin-3-yl)ethanol CAS 1355216-44-2

Purity 97%+In StockPharmaceutical Standards
CAS No.1355216-44-2
Molecular FormulaC12H20N2O
Molecular Weight208.30 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

1-(6-(tert-Butylamino)-4-methylpyridin-3-yl)ethanol CAS 1355216-44-2 chemical structure

Description

The occurrence of 1-(6-(tert-Butylamino)-4-methylpyridin-3-yl)ethanol is closely related to a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage in its molecular formula, which determines its behaviour during synthesis, purification, or degradation.

CATO supplies 1-(6-(tert-Butylamino)-4-methylpyridin-3-yl)ethanol (CAS 1355216-44-2), a certified reference material (molecular formula C12H20N2O, MW 208.30 g/mol) for analytical method development and quality control.

Owing to a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage, 1-(6-(tert-Butylamino)-4-methylpyridin-3-yl)ethanol is typically off-white to pale yellow low-melting solid. Its solid-state physicochemical attributes — including a molecular weight of 208.30 g/mol — guide the selection of appropriate sample preparation and analytical techniques. The aromatic system may exhibit native fluorescence, enabling detection with a fluorescence detector (FLD).

Recommended for analytical method development and validation; each product is supplied with a full Certificate of Analysis (COA) ensuring ISO 17034 metrological traceability.

CATO manufactures 1-(6-(tert-Butylamino)-4-methylpyridin-3-yl)ethanol under ISO 17034:2016 accreditation with dual CNAS and ANAB accreditation. Each batch is characterized by orthogonal methods and supplied with a full Certificate of Analysis (COA), ensuring metrological traceability.

Physical & Chemical Properties

Molecular FormulaC12H20N2O
Molecular Weight208.30 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light
Solubility (reference)Soluble in DMSO, DMF, methanol
StabilityLight-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)4.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1991
Nitrogen Atoms2

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