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O-Desmethylvenlafaxine

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Company Name: Shanghai Boyle Chemical Co., Ltd.  
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O-Desmethylvenlafaxine manufacturers

  • Desvenlafaxine
  • Desvenlafaxine pictures
  • $73.00
  • 2026-07-27
  • CAS:93413-62-8
  • Purity: 99.81%
  • Supply Ability: 10g
O-Desmethylvenlafaxine Basic information
Product Name:O-Desmethylvenlafaxine
Synonyms:O-DESMETHYL VENLAFAXINE-D10;DL-O-Desmethylvenlafaxin;4-[2-(Dimethylamino)-1-(1-hydroxycyclohexyl)ethyl]phenol;O-Desmethylvenlafaxine;Desvenlafaxine(O-Desnethylvenfaxine);1-[1-(4-Hydroxyphenyl)-2-dimethylaminoethyl]cyclohexanol;4-[1-(1-Hydroxycyclohexyl)-2-(dimethylamino)ethyl]phenol;Desmethylvenlafaxine
CAS:93413-62-8
MF:C16H25NO2
MW:263.38
EINECS:700-516-2
Product Categories:PRISTIQ;Metabolite & impurity;Metabolites;Intermediates & Fine Chemica;Pfizer Compounds;Amines;Aromatics;Intermediates & Fine Chemicals;Metabolites & Impurities;Pharmaceuticals
Mol File:93413-62-8.mol
O-Desmethylvenlafaxine Structure
O-Desmethylvenlafaxine Chemical Properties
Melting point 208-213°C
Boiling point 403.8±25.0 °C(Predicted)
density 1.115±0.06 g/cm3(Predicted)
Fp 9℃
storage temp. 2-8°C
solubility insoluble in EtOH; ≥13.2 mg/mL in DMSO; ≥2.45 mg/mL in EtOH
pka10.04±0.26(Predicted)
form Solid
color White to off-white
Major Applicationclinical testing
InChI1S/C16H25NO2/c1-17(2)12-15(13-6-8-14(18)9-7-13)16(19)10-4-3-5-11-16/h6-9,15,18-19H,3-5,10-12H2,1-2H3
InChIKeyKYYIDSXMWOZKMP-UHFFFAOYSA-N
SMILESN(CC(C2(CCCCC2)O)c1ccc(cc1)O)(C)C
LogP0.33 at 25℃ and pH6
Safety Information
Hazard Codes F,T,Xi
Risk Statements 11-23/24/25-39/23/24/25-36
Safety Statements 7-16-36/37-45-26
RIDADR UN1230 - class 3 - PG 2 - Methanol, solution
WGK Germany 3
RTECS GV8872620
HS Code 29225090
Storage Class11 - Combustible Solids
Hazard ClassificationsEye Irrit. 2
Hazardous Substances Data93413-62-8(Hazardous Substances Data)
MSDS Information
O-Desmethylvenlafaxine Usage And Synthesis
DescriptionDesvenlafaxine is a new member of the SNRI class of antidepressants. It is marketed as an extended release tablet for once-daily oral treatment of MDD in adult patients. Desvenlafaxine (O-desmethylvenlafaxine) is the major active metabolite of the previously marketed antidepressant venlafaxine (Effexor). Similar to venlafaxine, desvenlafaxine is a more potent inhibitor of serotonin and norepinephrine reuptake (IC50=47 and 531 nM, respectively) than that of dopamine (62% inhibition at 100 mM) in in vitro studies. It does not have significant in vitro affinity for other neurotransmitter reporters such as a1-adrenergic, H1-histaminergic, or muscarine-cholinergic receptors. Desvenlafaxine is marketed as a racemic mixture. Specific pharmacological properties of the enantiomers of desvenlafaxine have not been reported.
Chemical PropertiesWhite Solid
OriginatorWyeth (United States)
UsesA metabolite of Venlafaxine, a selective serotonin noradrenaline reuptake inhibitor. Used as an antidepressant
UsesA metabolite of Venlafaxine (V120000), a selective serotonin noradrenaline reuptake inhibitor (SNRI). Used as an antidepressant.
Usesa metabolite of Venlafaxine .;Labeled Venlafaxine, intended for use as an internal standard for the quantification of Venlafaxine by GC- or LC-mass spectrometry.
DefinitionChEBI: A tertiary amino compound that is N,N-dimethylethanamine substituted at position 1 by a 1-hydroxycyclohexyl and 4-hydroxyphenyl group. It is a metabolite of the drug venlafaxine.
Brand namePristiq
General DescriptionAn analytical reference standard applicable for use as starting material in calibrators or controls for a variety of LC/MS or GC/MS applications such as urine drug testing, forensic analysis, or clinical toxicology. Also known as desvenlafaxine, O-desmethylvenlafaxine is an SNRI antidepressant marketed under the trade name Pristiq for the treatment of depression. O-desmethylvenlafaxine is also a major urinary metabolite of venlafaxine, an SNRI antidepressant sold as Effexor or Efexor and used to treat major depressive disorder, generalized anxiety disorder, and other anxiety disorders associated with depression.
SynthesisDesvenlafaxine is chemically derived from 4-benzyloxyphenylacetic acid, by first converting to the acid chloride with oxalyl chloride and then condensing with dimethylamine to produce the corresponding N,N-dimethyl amide. Deprotonation of the amide with butyllithium, followed by condensation with cyclohexanone gives a b-hydroxyamide intermediate, which is reduced with alane, and debenzylated by using palladium on carbon and 1,4-cyclohexadiene to produce desvenlafaxine.
Tag:O-Desmethylvenlafaxine(93413-62-8) Related Product Information
Cyclohexanone Nonylphenol Phenol Phenol Red Ethylparaben Venlafaxine hydrochloride 1-Hydroxyethylidene-1,1-diphosphonic acid Ethyl acetate 4-Aminophenol Ethyl maltol Hydroxyethyl Cellulose Venlafaxine Hydroxyapatite type I Phenylacetone Cyclohexanol trans-4-Ethylcyclohexanol Desvenlafaxine succinate Monohydrate N-Boc N,O-Didesmethylvenlafaxine