Scopine - ≥98% , CAS No.498-45-3

CAS: 498-45-3 Cat. No.: S129883 Molecular Weight: 155.19 PubChem CID: 1274465
AVAILABLE TO ORDER
GRADE & PURITY ≥98%
Synonyms
3-Oxa-9-azatricyclo[3.3.1.02,4]nonan-7-ol, 9-methyl-, (1alpha,2beta,4beta,5alpha,7alpha)- | MFCD06658282 | PD087721 | CCG-266261 | FIMXSEMBHGTNKT-UPGAHCIJSA-N | Q7434451 | SW219096-1 | 1.ALPHA.H,5.ALPHA.H-TROPAN-3.ALPHA.-OL, 6.BETA.,7.BETA.-EPOXY- | s2545
Storage
Store at 2-8°C,Protected from light
Shipped In
Wet ice
 ·  off list, applied to all prices below.
Size
Status
Price
Qty
25mg
S129883-25mg
3
$124.90
100mg
S129883-100mg
3
$247.90
200mg
S129883-200mg
1
$323.90
500mg
S129883-500mg
2
$794.90
1g
S129883-1g
2
$948.90
Enter a quantity for the sizes you want to add.
🧪

Why this grade

≥98% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Store at 2-8°C,Protected from light Ships Wet ice Check lot-specific COA for exact specifications.

📋

Quality documents

SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.

📚

Literature proof

Cited in 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Overview

Scopine is the metabolite of anisodine, which is a α1-adrenergic receptor agonist and used in the treatment of acute circulatory shock.
A metabolite of scopolamine

Specifications

Synonyms
3-Oxa-9-azatricyclo[3.3.1.02, 4]nonan-7-ol, 9-methyl-, (1alpha, 2beta, 4beta, 5alpha, 7alpha)- | MFCD06658282 | PD087721 | CCG-266261 | FIMXSEMBHGTNKT-UPGAHCIJSA-N | Q7434451 | SW219096-1 | 1.ALPHA.H, 5.ALPHA.H-TROPAN-3.ALPHA.-OL, 6.BETA., 7.BETA.-EPOXY- | s2545
Specifications & Purity
≥98%
Biochemical and Physiological Mechanisms
Scopine is a tropane alkaloid and a metabolite of scoplamone.Tropane Alkaloid. Metabolite of scopolamine. Active in vivo and in vitro .
Storage
Store at 2-8°C, Protected from light
Shipped In
Wet ice
This product requires cold chain shipping. Ground and other economy services are not available.
Note
Wherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20°C. Generally, these will be useable for up to one month. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour. Need more advice on solubility, usage and handling? Please visit our frequently asked questions (FAQ) page for more details.
Purity
≥98%
Names and Identifiers
Pubchem Sid504760454
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/504760454
Canonical SmilesCN1C2CC(CC1C3C2O3)O
IUPAC Name(1R,2R,4S,5S)-9-methyl-3-oxa-9-azatricyclo[3.3.1.02,4]nonan-7-ol
InChIKeyFIMXSEMBHGTNKT-UPGAHCIJSA-N
INCHI1S/C8H13NO2/c1-9-5-2-4(10)3-6(9)8-7(5)11-8/h4-8,10H,2-3H2,1H3/t4?,5-,6+,7-,8+
Isomeric SMILES CN1[C@@H]2CC(C[C@H]1[C@H]3[C@@H]2O3)O
PubChem CID 1274465
Molecular Weight 155.19

Documentation

📋 Safety Data Sheet (SDS)

Comprehensive hazard, handling, storage, and regulatory compliance document.

Download SDS →

✅ Certificate of Analysis (COA)

Lot-specific quality data. Enter your lot number to retrieve the exact COA.

Look up COA →

📊 Datasheet

Quick-reference summary of product specifications and applications.

View datasheet →

🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

View spec sheet →

Advanced Data

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassOrganoheterocyclic compounds
ClassOxazinanes
SubclassMorpholines
Intermediate Tree Nodes Not available
Direct ParentMorpholines
Alternative Parents Piperidines  N-alkylpyrrolidines  Trialkylamines  Secondary alcohols  Cyclic alcohols and derivatives  Oxacyclic compounds  Epoxides  Dialkyl ethers  Azacyclic compounds  Organopnictogen compounds  Hydrocarbon derivatives  
Molecular FrameworkAliphatic heteropolycyclic compounds
Substituents Morpholine - Piperidine - N-alkylpyrrolidine - Cyclic alcohol - Pyrrolidine - Secondary alcohol - Tertiary amine - Tertiary aliphatic amine - Dialkyl ether - Oxirane - Ether - Oxacycle - Azacycle - Organonitrogen compound - Organic oxygen compound - Amine - Organooxygen compound - Organopnictogen compound - Hydrocarbon derivative - Organic nitrogen compound - Alcohol - Aliphatic heteropolycyclic compound
DescriptionThis compound belongs to the class of organic compounds known as morpholines. These are organic compounds containing a morpholine moiety, which consists of a six-member aliphatic saturated ring with the formula C4H9NO, where the oxygen and nitrogen atoms lie at positions 1 and 4, respectively.
External Descriptors Not available
3D Structure
Interactive Chemical Structure Model





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.

5 results found

Lot NumberCertificate TypeDateItem
I2227599Certificate of AnalysisApr 03, 2026 S129883
I2227629Certificate of AnalysisApr 03, 2026 S129883
I2227630Certificate of AnalysisApr 03, 2026 S129883
I2227631Certificate of AnalysisApr 03, 2026 S129883
I2227632Certificate of AnalysisApr 03, 2026 S129883
Chemical and Physical Properties
SolubilityDMSO 31 mg/mL Water 31 mg/mL Ethanol 31 mg/mL
SensitivityLight sensitive
Molecular Weight155.190 g/mol
XLogP3-0.200
Hydrogen Bond Donor Count1
Hydrogen Bond Acceptor Count3
Rotatable Bond Count0
Exact Mass155.095 Da
Monoisotopic Mass155.095 Da
Topological Polar Surface Area36.000 Ų
Heavy Atom Count11
Formal Charge0
Complexity179.000
Isotope Atom Count0
Defined Atom Stereocenter Count4
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count1
Solution Calculators
Reviews

Customer Reviews

Shall we send you a message when we have discounts available?

Remind me later

Thank you! Please check your email inbox to confirm.

Oops! Notifications are disabled.