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· · COA & SDS available for every product · Same-day shipping on in-stock items Gelsemine - 10mM in DMSO , CAS No.509-15-9
GRADE & PURITY 10mM in DMSO
Synonyms
GELSEMINE|509-15-9|Gelsemin|5Y13A78Z72|NSC-21729|UNII-5Y13A78Z72|HSDB 3488|gelsemine free base|(+)-Gelsemine|EINECS 208-095-2|NSC 21729|BRN 5406576|GELSEMIN [HSDB]|GELSEMINE [MI]|GELSEMINE [WHO-DD]|GELSEMINE, (+)-|(3R-(3alpha,4abeta,5alpha,8alpha,8abeta,9
Shipped In
Dry ice packs + Cold packs
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Why this grade 10mM in DMSO for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
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Storage & shipping Store at -80°C Ships Dry ice packs + Cold packs Check lot-specific COA for exact specifications.
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Quality documents SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.
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Literature proof Cited in 1 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Overview Gelsemine is a CNS stimulant derived from the roots and rhizome of Gelsemium sempervirens.
Specifications Synonyms
GELSEMINE | 509-15-9 | Gelsemin | 5Y13A78Z72 | NSC-21729 | UNII-5Y13A78Z72 | HSDB 3488 | gelsemine free base | (+)-Gelsemine | EINECS 208-095-2 | NSC 21729 | BRN 5406576 | GELSEMIN [HSDB] | GELSEMINE [MI] | GELSEMINE [WHO-DD] | GELSEMINE, (+)- | (3R-(3alpha, 4abeta, 5alpha, 8alpha, 8abeta, 9
Specifications & Purity
10mM in DMSO
Shipped In
Dry ice packs + Cold packs
This product requires cold chain shipping. Ground and other economy services are not available.
Names and Identifiers Canonical Smiles CN1CC2(C3CC4C5(C2C1C3CO4)C6=CC=CC=C6NC5=O)C=C IUPAC Name (1'R,2'S,3S,5'S,6'S,8'R,11'S)-2'-ethenyl-4'-methylspiro[1H-indole-3,7'-9-oxa-4-azatetracyclo[6.3.1.02,6.05,11]dodecane]-2-one InChIKey NFYYATWFXNPTRM-QJICHLCESA-N INCHI 1S/C20H22N2O2/c1-3-19-10-22(2)16-11-9-24-15(8-13(11)19)20(17(16)19)12-6-4-5-7-14(12)21-18(20)23/h3-7,11,13,15-17H,1,8-10H2,2H3,(H,21,23)/t11-,13+,15+,16+,17-,19-,20-/m0/s1 Isomeric SMILES CN1C[C@]2([C@@H]3C[C@@H]4[C@]5([C@H]2[C@H]1[C@H]3CO4)C6=CC=CC=C6NC5=O)C=C Molecular Weight 322.4 Reaxy-Rn 102312 Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=102312&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 Kingdom Organic compounds Superclass Alkaloids and derivatives Class Gelsemium alkaloids Subclass Not available Intermediate Tree Nodes Not available Direct Parent Gelsemium alkaloids Alternative Parents Indolines Isoindolines Aralkylamines Oxepanes Benzenoids Piperidines Oxanes N-alkylpyrrolidines Amino acids and derivatives Trialkylamines Secondary carboxylic acid amides Lactams Dialkyl ethers Oxacyclic compounds Azacyclic compounds Carbonyl compounds Hydrocarbon derivatives Organic oxides Molecular Framework Aromatic heteropolycyclic compounds Substituents Gelsemium skeleton - Indole or derivatives - Dihydroindole - Isoindoline - Isoindole or derivatives - Aralkylamine - Oxepane - Benzenoid - N-alkylpyrrolidine - Piperidine - Oxane - Pyrrolidine - Carboxamide group - Amino acid or derivatives - Lactam - Tertiary aliphatic amine - Tertiary amine - Secondary carboxylic acid amide - Oxacycle - Azacycle - Carboxylic acid derivative - Dialkyl ether - Ether - Organoheterocyclic compound - Amine - Organic oxide - Organic oxygen compound - Hydrocarbon derivative - Carbonyl group - Organic nitrogen compound - Organonitrogen compound - Organooxygen compound - Aromatic heteropolycyclic compound Description This compound belongs to the class of organic compounds known as gelsemium alkaloids. These are alkaloids with a structure that is based on the tetracyclic gelsemium skeleton. These alkaloids contain an oxindole function and a cage-like, hydroaromatic residue which is believed to arise from an intermediate related to anhydrovobasinediol by formation of a 6,20 bond and rearrangement to an oxindole. The major alkaloids in this group are related to Gelsemine; however, a smaller group, characterized by Gelsedine, lack the 6,20 bond, and have also lost C-21. External Descriptors Indole alkaloids Data sources 1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.
3D Structure Associated Targets(Human) Associated Targets(non-human) Mechanisms of Action Certificates（CoA,COO,BSE/TSE and Analysis Chart) Chemical and Physical Properties Melt Point(°C) 180-181° C Molecular Weight 322.400 g/mol XLogP3 1.800 Hydrogen Bond Donor Count 1 Hydrogen Bond Acceptor Count 3 Rotatable Bond Count 1 Exact Mass 322.168 Da Monoisotopic Mass 322.168 Da Topological Polar Surface Area 41.600 Ų Heavy Atom Count 24 Formal Charge 0 Complexity 635.000 Isotope Atom Count 0 Defined Atom Stereocenter Count 7 Undefined Atom Stereocenter Count 0 Defined Bond Stereocenter Count 0 Undefined Bond Stereocenter Count 0 The total count of all stereochemical bonds 0 Covalently-Bonded Unit Count 1
Citations of This Product References 1. Xinghua Liu, Lingpeng Yan, Jingxia Zheng, Yongzhen Yang, Xuguang Liu, Bingshe Xu. (2023) Highly optically and thermally stable carbon dots enabled by thermal annealing for laser illumination. Journal of Materials Chemistry C, 11 (10): (3562-3570). [PMID: [10.1039/D2TC05359D ]
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