3-Hydroxyquinuclidine
3-Hydroxyquinuclidine, synonymous with 3-quinuclidinol, is the bicyclic alcohol with nitrogen hetero-atom and hydrogenated pyridine ring under HTS 2933.35.00.00. Synthetic intermediate for muscarinic receptor pharmaceuticals.
Import Duty Rates by Country of Origin
| Origin Country | MFN Rate | Ch.99 Surcharges | Total Effective Rate |
|---|---|---|---|
| π¨π³China | 5.8% | β | 5.8% |
| π²π½Mexico | 5.8% | β | 5.8% |
| π¨π¦Canada | 5.8% | β | 5.8% |
| π©πͺGermany | 5.8% | β | 5.8% |
| π―π΅Japan | 5.8% | β | 5.8% |
Alternative Classifications
This product could be classified differently depending on its characteristics or intended use.
If classified as alkaloid derivative
Vegetable alkaloid-like structures sometimes shift to 2939 despite synthetic origin.
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Import Tips & Compliance
β’ Use CAS 1619-34-7 in all documentation for unambiguous identification
β’ For R&D imports, include end-user statement to qualify for lower duties if applicable
Related Products under HTS 2933.35.00.00
3-Quinuclidinol
3-Quinuclidinol is a bicyclic heterocyclic alcohol containing a nitrogen hetero-atom and an unfused pyridine ring structure (hydrogenated form), classified under HTS 2933.35.00.00 as a specific compound with nitrogen hetero-atoms only. It serves as a key chiral building block in pharmaceutical synthesis.
3-Quinuclidinol Hydrochloride
3-Quinuclidinol hydrochloride is the salt form of the pyridine-nitrogen heterocyclic alcohol, classified under HTS 2933.35.00.00 per Chapter 29 rules for organic salts. Commonly used as a stable intermediate in drug manufacturing.
(R)-3-Quinuclidinol
(R)-3-Quinuclidinol is the enantiomerically pure R-form of the bicyclic alcohol with nitrogen hetero-atom and pyridine ring, directly matching HTS 2933.35.00.00. It's essential for synthesizing anticholinergic drugs like solifenacin used in overactive bladder treatment.
(S)-3-Quinuclidinol
(S)-3-Quinuclidinol represents the S-enantiomer of this nitrogen-heterocyclic alcohol with pyridine ring, under HTS 2933.35.00.00. Used in synthesis of pharmaceutical intermediates for CNS-active compounds.