3-(1,2,3,4-Tetrahydroquinolin-1-yl)propan-1-ol CAS 88014-20-4

Purity 97%+In StockPharmaceutical Standards
CAS No.88014-20-4
Molecular FormulaC12H17NO
Molecular Weight191.27 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

3-(1,2,3,4-Tetrahydroquinolin-1-yl)propan-1-ol CAS 88014-20-4 chemical structure

Description

Under current pharmacopoeial and regulatory frameworks, quality-control requirements for this class of reference material explicitly involve the control of targets including 3-(1,2,3,4-Tetrahydroquinolin-1-yl)propan-1-ol.

CATO supplies 3-(1,2,3,4-Tetrahydroquinolin-1-yl)propan-1-ol (CAS 88014-20-4), a certified reference material (molecular formula C12H17NO, MW 191.27 g/mol) for analytical method development and quality control.

Based on its molecular formula C12H17NO, 3-(1,2,3,4-Tetrahydroquinolin-1-yl)propan-1-ol contains a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage; these features give the compound characteristic absorption bands in UV spectroscopy. The molecular weight of 191.27 g/mol is directly relevant to the identification of the molecular ion in mass spectrometry. 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 3-(1,2,3,4-Tetrahydroquinolin-1-yl)propan-1-ol 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 FormulaC12H17NO
Molecular Weight191.27 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate, DMSO
StabilityLight-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)5.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1982
Nitrogen Atoms1

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