Morphodrol, ≥98%
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Morpholin-3-yl pipradol variant; putative catecholamine reuptake inhibitor with psychostimulant action of possibly reduced potency and shorter half life.
Chemical Name | 3-(diphenylhydroxymethyl)morpholine |
Synonyms | α,α-Diphenyl-3-morpholinemethanol, morpholin-3-yl-diphenyl-methanol, α-Morpholyl-(3)-benzhydrol |
CAS # | 26581-79-3 |
Form | Off-white powder |
Molecular Formula | C17H19NO2 |
Molecular Weight | 269.34 g/mol |
Melting Point | 129-131 °C |
Solubility | Soluble in Ethanol |
Precaution and Disclaimer:
This Material is Sold For Research Use Only. Terms of Sale Apply. Not for Human Consumption, nor Medical, Veterinary, or Household Uses.
Chemical Information:
CAS Number: | 26581-79-3 |
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Purity: | ≥98% |
Molecular Weight: | 269.34 g/mol |
Melting Point: | + 129-131 °C |
Molecular Formula: | C17H19NO2 |
Synonyms: | 3-(diphenylhydroxymethyl)morpholine; α,α-Diphenyl-3-morpholinemethanol; morpholin-3-yl-diphenyl-methanol; α-Morpholyl-(3)-benzhydrol |
PubChem CID: | 73062393 |
SMILES: | C1COCC(N1)C(C2=CC=CC=C2)(C3=CC=CC=C3)O |
Technical Information:
Application: | Morpholin-3-yl pipradol variant; putative catecholamine reuptake inhibitor with psychostimulant action of possibly reduced potency and shorter half life. |
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Appearance: | Off-White powder |
Physical State: | Solid |
Solubility: | Soluble in Ethanol |
Storage: | Store in dry, dark conditions at 0 – 4 °C for short-term (weeks), and - 20°C for long term storage. |
Stability: | Stable for at least three years when stored as unopened at 0 – 4 °C |
Background:
Morpholin-3-yl pipradol variant; putative catecholamine reuptake inhibitor with psychostimulant action of possibly reduced potency and shorter half life than pipradol. Interestingly, in contrast to most psychostimulants, this compound potentiated pentobarbital induced hypnosis in addition to antagonizing bulbocapnine induced catatonia[1],[3].
References:
- [1] Winthrop, Stanley O.. alpha-(3-morpholyl)-
benzhydrol and its salts . American Home Products, assignee. Patent US2947749. 2 Aug. 1960. - [2] National Center for Biotechnology Information. PubChem Database. CID=73062393, https://pubchem.ncbi.nlm.nih.gov/compound/Morpholin-3-yl_diphenyl_methanol
- [3] WINTHROP, STANLEY O., and LESLIE G. HUMBER. “Central Stimulants. Cyclized Diphenylisopropylamines.” The Journal of Organic Chemistry 26, No. 8 (August 1, 1961): 2834–36. https://doi.org/10.1021/jo01066a051.
- [4] White, Michael W., and John R. H. Archer. “Chapter 10 - Pipradrol and Pipradrol Derivatives.” In Novel Psychoactive Substances, edited by Paul I. Dargan and David M. Wood, 233–59. Boston: Academic Press, 2013. https://doi.org/10.1016/B978-0-12-415816-0.00010-9.
Precaution and Disclaimer:
This Material is Sold For Research Use Only. Terms of Sale Apply. Not for Human Consumption, nor Medical, Veterinary, or Household Uses.
[Morphodrol Q1 2019] Morphodrol.20181107.pdf
[Morphodrol Q4 2018] Morphodrol.20180910.pdf
[Morphodrol Q4 2018] Morphodrol.20181107.pdf