Myosmine - ≥98% , CAS No.532-12-7

CAS: 532-12-7 Cat. No.: M342525 Peso molecular: 146.19 Beilstein Registry Number: 119254 Número EC: 637-297-7
Disponible para pedir
GRADE & PURITY ≥98%
Synonyms
9O0A545W4L | HY-W001909 | Pyridine, 3-(1-pyrrolin-2-yl)- | BPBio1_000719 | Prestwick2_000647 | 3-(1-Pyrrolin-2-yl)pyridine, 8CI | BDBM50125053 | KBio2_004178 | STL554354 | 1-AMINO-CYCLOPENT-3-ENECARBOXYLICACID | 3-(3,4-Dihydro-2H-pyrrol-5-yl)pyridine, 9CI
Storage
Store at 2-8°C
Shipped In
Wet ice
 ·  off list, applied to all prices below.
Size
Estado
Price
Qty
100mg
M342525-100mg
3
102,90US$
250mg
M342525-250mg
3
125,90US$
500mg
M342525-500mg
3
222,90US$
1g
M342525-1g
2
344,90US$
5g
M342525-5g
2
1.183,90US$
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 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 1 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Descripción general

Product Description

Myosmine is a minor tobacco alkaloid which has been shown to possess genotoxic effects on cells through DNA damage by pyridyloxobutylation. Studies indicate that in cells Myosmine can be activated into reactive intermediates by H|2|O|2| and 3-morpholinosydnonimine . It is known that under acidic pH Myosmine undergoes a ring-chain tautomerism and is present in the amino-keto form. Furthermore, Myosmine is an ideal tool to use to monitor the effects of tobacco smoke on cells.

Product Application
Nitrosation reactions;Peroxidation reaction with hydrogen peroxide


Specifications

Sinónimos
9O0A545W4L | HY-W001909 | Pyridine, 3-(1-pyrrolin-2-yl)- | BPBio1_000719 | Prestwick2_000647 | 3-(1-Pyrrolin-2-yl)pyridine, 8CI | BDBM50125053 | KBio2_004178 | STL554354 | 1-AMINO-CYCLOPENT-3-ENECARBOXYLICACID | 3-(3, 4-Dihydro-2H-pyrrol-5-yl)pyridine, 9CI
Especificaciones y pureza
≥98%
Condiciones de almacenamiento de almacenamiento
Store at 2-8°C
Enviado en
Wet ice
Este producto requiere envío en cadena de frío. Los servicios terrestres y otros servicios económicos no están disponibles.
Pureza
≥98%
Nombres e identificadores
Pubchem Sid504758787
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/504758787
Sonrisas canónicasC1CC(=NC1)C2=CN=CC=C2
IUPAC Name3-(3,4-dihydro-2H-pyrrol-5-yl)pyridine
InChIKeyDPNGWXJMIILTBS-UHFFFAOYSA-N
INCHI1S/C9H10N2/c1-3-8(7-10-5-1)9-4-2-6-11-9/h1,3,5,7H,2,4,6H2
Isómeros SMILES C1CC(=NC1)C2=CN=CC=C2
RTECS UT7660000
Peso molecular 146.19
Beilstein 119254
Reaxy-Rn 119254
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=119254&ln=

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
ClasePyridines and derivatives
SubclassNot available
Intermediate Tree Nodes Not available
Direct ParentPyridines and derivatives
Alternative Parents Pyrrolines  Heteroaromatic compounds  Ketimines  Propargyl-type 1,3-dipolar organic compounds  Azacyclic compounds  Organopnictogen compounds  Hydrocarbon derivatives  
Molecular FrameworkAromatic heteromonocyclic compounds
Substituents Pyridine - Heteroaromatic compound - Pyrroline - Ketimine - Azacycle - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Organic nitrogen compound - Organopnictogen compound - Hydrocarbon derivative - Organonitrogen compound - Imine - Aromatic heteromonocyclic compound
DescripciónThis compound belongs to the class of organic compounds known as pyridines and derivatives. These are compounds containing a pyridine ring, which is a six-member aromatic heterocycle which consists of one nitrogen atom and five carbon atoms.
External Descriptors Pyridine alkaloids
Estructura 3D
Modelo de Estructura Química Interactiva





Objetivos asociados (humanos)
ACHE Tclin Acetylcholinesterase (18204 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
THRB Tclin Thyroid hormone receptor beta-1 (7926 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ALDH1A1 Tchem Aldehyde dehydrogenase 1A1 (77053 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CYP2D6 Tclin Cytochrome P450 2D6 (33882 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CYP1A2 Tchem Cytochrome P450 1A2 (26471 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CYP2C9 Tchem Cytochrome P450 2C9 (32119 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CYP2C19 Tchem Cytochrome P450 2C19 (29246 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CYP3A4 Tclin Cytochrome P450 3A4 (53859 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CYP2A6 Tchem Cytochrome P450 2A6 (2861 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CHRNB2 Tclin Neuronal acetylcholine receptor; alpha4/beta2 (3972 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Objetivos asociados (no humanos)
Musca domestica (713 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
nAChRalpha5 Nicotinic acetylcholine receptor alpha 5 subunit (134 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Nicotinic acetylcholine receptor alpha8 subunit (79 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mecanismos de acción
Certificados (CoA, COO, BSE/TSE y tabla de análisis)
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 TypeFechaArticulo
G2221014Certificate of AnalysisMay 09, 2025 M342525
G2221019Certificate of AnalysisMay 09, 2025 M342525
G2221021Certificate of AnalysisMay 09, 2025 M342525
G2221022Certificate of AnalysisMay 09, 2025 M342525
G2221023Certificate of AnalysisMay 09, 2025 M342525
Propiedades químicas y físicas
SolubilidadSoluble in Ether, Ethyl Acetate, Methanol and Water
Punto de fusión (°C)42-44° C
Peso molecular146.190 g/mol
XLogP30.600
Hydrogen Bond Donor Count0
Hydrogen Bond Acceptor Count2
Rotatable Bond Count1
Exact Mass146.084 Da
Monoisotopic Mass146.084 Da
Topological Polar Surface Area25.300 Ų
Heavy Atom Count11
Formal Charge0
Complexity163.000
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count1
Citations of This Product
Referencias
1. Chencheng Dai, Yiwei Cao, Yiran Xu, Moyuan Li, Guangquan Liu, Sujuan Xu, Nuo Ye, Changxiang Shi, Tiantian Fan, Pengfei Xu, Xuemei Jia.  (2026)  Serum metabolic fingerprinting for diagnosis and therapeutic applications of ovarian endometriosis.  iScience,  29  (3):   [PMID:41743236] [10.1016/j.isci.2026.114887]
Calculadoras de soluciones
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