25H-NBOMe imine analog

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Cat No: 12062

Biochemicals - Drugs Of Abuse

2C-H, also known as 25H or 2,5-dimethoxyphenethylamine, (Item No. 11889) is a phenethylamine that has little effect on serotonin receptors, activating the 5-HT2C receptor to 20% that induced by serotonin (pEC50 = 5.93).{20772} The addition of N-(2-meth...

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Territorial Availability: Available through Bertin Technologies only in France

                                            Technical Warning: Bertin Technologies restricts the sale of this product to licensed controlled substance laboratories and qualified academic research institutions. Please contact us for further details.
                    

                        Special Advice: Please check regulation status before ordering; additionel fees can apply. 
                    

Synonyms:

(E)-2-(2,5-dimethoxyphenyl)-N-(2-methoxybenzylidene)ethanamine

Correlated keywords:

phenethylamines designer drugs forensics receptors agonists serotonins 5-HT 5-HT2A 2C-H 2CH 5HT 5HT2A 25H 25-H 2,5-dimehoxyphenethylamine 5HT2C 5-HT2C analytical references standards

Product Overview:
2C-H, also known as 25H or 2,5-dimethoxyphenethylamine, (Item No. 11889) is a phenethylamine that has little effect on serotonin receptors, activating the 5-HT2C receptor to 20% that induced by serotonin (pEC50 = 5.93).{20772} The addition of N-(2-methoxybenzyl) at the amine increases the affinity for the 5-HT2A receptor over other serotonin receptors (Ki values for 25H and 25H-NBOMe are 227 and 1.19 nM, respectively).{20442} 25H-NBOMe imine analog differs from 25H-NBOMe by having a double bond linking the N-(2-methoxybenzyl) group to 25H. The properties of this compound have not been evaluated. This product is intended for research and forensic applications.

Size	1 mg
Shipping	dry ice
CAS Number	1566571-78-5
Molecular Formula	C₁₈H₂₁NO₃
SMILES	COC1=C(CC/N=C/C2=C(OC)C=CC=C2)C=C(OC)C=C1
Molecular Weight	299,4
Formulation	A solution in methyl acetate
Purity	≥95%
Custom Code	2932.99
UNSPSC code	12352100

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Cayman Chemical's mission is to help make research possible by supplying scientists worldwide with the basic research tools necessary for advancing human and animal health. Our utmost commitment to healthcare researchers is to offer the highest quality products with an affordable pricing policy.

Our scientists are experts in the synthesis, purification, and characterization of biochemicals ranging from small drug-like heterocycles to complex biolipids, fatty acids, and many others. We are also highly skilled in all aspects of assay and antibody development, protein expression, crystallization, and structure determination.

Over the past thirty years, Cayman developed a deep knowledge base in lipid biochemistry, including research involving the arachidonic acid cascade, inositol phosphates, and cannabinoids. This knowledge enabled the production of reagents of exceptional quality for cancer, oxidative injury, epigenetics, neuroscience, inflammation, metabolism, and many additional lines of research.

Our organic and analytical chemists specialize in the rapid development of manufacturing processes and analytical methods to carry out clinical and commercial GMP-API production. Pre-clinical drug discovery efforts are currently underway in the areas of bone restoration and repair, muscular dystrophy, oncology, and inflammation. A separate group of Ph.D.-level scientists are dedicated to offering Hit-to-Lead Discovery and Profiling Services for epigenetic targets. Our knowledgeable chemists can be contracted to perform complete sample analysis for analytes measured by the majority of our assays. We also offer a wide range of analytical services using LC-MS/MS, HPLC, GC, and many other techniques.

Accreditations
ISO/IEC 17025:2005
ISO Guide 34:2009

Cayman is a leader in the field of emerging drugs of abuse, providing high-purity Schedule I-V Controlled Substances to federally-licensed laboratories and qualified academic research institutions for forensic analyses. We are certified by ACLASS Accreditation Services with dual accreditation to ISO/IEC 17025:2005 and ISO Guide 34:2009.