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M3196 Sigma

5-MEO-DIPT hydrochloride hydrate

Synonym: Methoxy Foxy, N,N-Diisopropyl-5-methoxytryptamine hydrochloride hydrate

  • Empirical Formula (Hill Notation) C17H26N2O · xHCl · yH2O

  • Molecular Weight 274.40 (anhydrous free base basis)

  •  MDL number MFCD12912426

  •  PubChem Substance ID 329817965

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Properties

Related Categories Agonists, Bioactive Small Molecule Alphabetical Index, Bioactive Small Molecules, Cell Biology, Cell Signaling and Neuroscience,
InChI Key   DFERASOFTGVIPG-UHFFFAOYSA-N
drug control   USDEA Schedule I
storage temp.   room temp

Description

Biochem/physiol Actions

5-MeO-DIPT is a tryptamine derivative. In animal behavioral studies, 5-MeO-DIPT has been shown to produce behavioral effects that are substantially similar to those of LSD, both schedule I hallucinogens.

Features and Benefits

This compound is featured on the Biogenic Amine Transporters page of the Handbook of Receptor Classification and Signal Transduction. To browse other handbook pages, click here.

Safety & Documentation

Safety Information

Symbol 
GHS07  GHS07
Signal word 
Warning
Hazard statements 
Precautionary statements 
Personal Protective Equipment 
RIDADR 
NONH for all modes of transport
WGK Germany 
3

Documents

Certificate of Analysis

Certificate of Origin


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Protocols & Articles

Articles

Biogenic Amine Transporters

Following vesicular release, the biogenic amine neurotransmitters, norepinephrine (A7257), dopamine (H8502) and serotonin (H9523), are removed from the extracellular space by selective and pharmacolo...
Keywords: Anti-depressants, Atomic absorption spectroscopy, Clinical, Cloning, Gene expression, Ligands, Neurotransmission, Neurotransmitters, Parkinson Disease, Phosphorylations, Schizophrenia

Serotonin Receptors

Serotonin (5-hydroxytryptamine, 5-HT) is widely distributed throughout the mammalian body, being synthesized from L-tryptophan in enterochromaffin cells of the gastro-intestinal tract as well as in s...
Keywords: Active transport, Atomic absorption spectroscopy, Cancer, Clinical, Gene expression, Ligands, Neurotransmitters, Obesity, Polymorphisms, Schizophrenia, Transduction

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