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Chemical substance record

Pindolol

13523-86-9C14H20N2O2248.326 g/mol

A member of the class of indols which is the 2-hydroxy-3-(isopropylamino)propyl ether derivative of 1H-indol-4-ol. — ChEBI

Safety references

Safety documents & references

1 indexed references
JP · NITE

Government GHS classification

23A5144 · FY2011

View classification

Find a product-specific SDS

Safety guides and government classification records are not a manufacturer’s SDS. Match supplier, product number, concentration, physical form, region and revision before using a document.

Identity & molecular properties

Source-linked values
CAS number13523-86-9ChEBI ↗
Molecular formulaC14H20N2O2ChEBI ↗
Molar mass248.326 g/molChEBI ↗
Monoisotopic mass248.15248 DaChEBI ↗
Formal charge0ChEBI ↗
ChEBI identifierCHEBI:8214ChEBI ↗

Cross-source molecular data

PubChem
Molar mass248.32 g/molPubChem ↗
Exact mass248.152477885 DaPubChem ↗
Computed XLogP1.8PubChem ↗
Topological polar surface area (Ų)57.3PubChem ↗
H-bond donors3PubChem ↗
H-bond acceptors3PubChem ↗
Rotatable bonds6PubChem ↗

PubChem computed values are shown separately from the ChEBI record. An exact InChIKey match was used to connect the records. Molecular descriptors do not describe a supplied product’s purity, particle size or performance.

Names & structural identifiers

Copy any identifier
pindolol
1-(1H-indol-4-yloxy)-3-[(propan-2-yl)amino]propan-2-ol
JZQKKSLKJUAGIC-UHFFFAOYSA-N
CC(C)NCC(O)COc1cccc2nccc12
InChI=1S/C14H20N2O2/c1-10(2)16-8-11(17)9-18-14-5-3-4-13-12(14)6-7-15-13/h3-7,10-11,15-17H,8-9H2,1-2H3

Names & synonyms

1-(1H-indol-4-yloxy)-3-[(propan-2-yl)amino]propan-2-olBetapindolBlockin LBlocklin LBlocklin-LCalviskenCardilateCarviskenDecretenDurapindolGlauco-ViskenPectobloc

Names are supplied by ChEBI. Trade names and related synonyms may describe a broader product context.

Classification & relationships

ChEBI ontology

Roles recorded in ChEBI

antidepressantbeta-adrenergic antagonistcardiovascular drugvasodilator agentantihypertensive agentantiglaucoma drugserotonergic antagonist

Database role annotations describe reported biological or chemical roles; they are not product approvals or recommendations for use.

Safety classification · Japan

NITE / Japanese government
Japan · FY2011 source classification
Pindolol · 23A5144
EndpointReported classification
Acute toxicity (Oral)Category 3
Reproductive toxicityCategory 2, Additional category: Effects on or via lactation
Specific target organ toxicity - Single exposureCategory 1 (cardiovascular system, nervous system)
Specific target organ toxicity - Repeated exposureCategory 1 (cardiovascular system, nervous system)

Selected source-reported endpoints. Other endpoints, rationales and conditions remain in the original classification. Missing or unlisted information does not mean non-hazardous. This is not a global classification or transport decision.

Read the original NITE classification

Mass ↔ amount of substance

Calculated from sourced mass
Equivalent amount
0.00402696 mol

Uses 248.326 g/mol from ChEBI. Assumes the substance described by this record; no purity or concentration correction is applied.

Elemental composition

Theoretical mass fractions
C
Carbon · 14 atoms
67.72%
O
Oxygen · 2 atoms
12.89%
N
Nitrogen · 2 atoms
11.28%
H
Hydrogen · 20 atoms
8.12%

Calculated theoretical mass fractions from the reported formula and PubChem periodic-table atomic masses. These are not assay or purity results.

Research & patent references

Selected source associations
Effects of sustained (+/-)pindolol administration on serotonin neurotransmission in rats. ↗Journal of psychiatry & neuroscience : JPN · 2000 Sep · PMID 11022403
NL6601040 · Patent reference ↗Patent cross-reference supplied by ChEBI. Association alone does not establish claim scope.

Sources & record history

Checked 27 Sep 2026
EMBL-EBI ChEBI · CHEBI:8214

Release 255, 9 September 2026. ChEBI three-star (manually annotated) source entry. View original record ↗ · CC BY 4.0

NCBI PubChem · CID 4828 · retrieved 2026-09-27

PubCAS formats source data, connects references and computes explicitly labelled conversions. CAS cross-references are supplied by ChEBI; they do not constitute CAS verification or endorsement.