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Moligand™, 10mM in DMSO Moligand™ for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Store at -80°C Ships Dry ice packs + Cold packs Check lot-specific COA for exact specifications.
SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.
Cited in 5 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
D,L-Venlafaxine is an isomer of Venlafaxine . Venlafaxine is a derivative of phenylethylamine which is reported to facilitate neurotransmission within the central nervous system via blocking the presynaptic reuptake of neuroamines such as serotonin (5-hydroxytryptamine; 5-HT) and noradrenaline (norepinephrine). Velanfaxine is also reported to be a weak inhibitor of dopamine reuptake.|In vitro|studies indicate that Venlafaxine does not demonstrate significant activity for muscarinic, histaminergic or α-1 adrenergic receptors. The metabolism of venlafaxine is reported to occur by cytochrome P450 (CYP) enzyme CYP2D6 yielding O-desmethylvenlafaxine. A lesser metabolite, N-desmethylvenlafaxine is produced by CYP3A4.
| pKa | pKₐ: 9.27 (Predicted) |
|---|---|
| Datos Ki | Norepinephrine transporter: Ki= 138 nM (rat); Serotonin transporter: Ki= 52 nM (rat); Dopamine transporter: Ki= 360 nM (rat) |
| Sonrisas canónicas | CN(C)CC(C1=CC=C(C=C1)OC)C2(CCCCC2)O |
|---|---|
| IUPAC Name | 1-[2-(dimethylamino)-1-(4-methoxyphenyl)ethyl]cyclohexan-1-ol |
| InChIKey | PNVNVHUZROJLTJ-UHFFFAOYSA-N |
| INCHI | 1S/C17H27NO2/c1-18(2)13-16(17(19)11-5-4-6-12-17)14-7-9-15(20-3)10-8-14/h7-10,16,19H,4-6,11-13H2,1-3H3 |
| Isómeros SMILES | CN(C)CC(C1=CC=C(C=C1)OC)C2(CCCCC2)O |
| RTECS | GV8872620 |
| Peso molecular | 277.4 |
| Beilstein | 4234848 |
| Reaxy-Rn | 4234848 |
| Reaxys-RN_link_address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=4234848&ln= |
Comprehensive hazard, handling, storage, and regulatory compliance document.
Download SDS →Lot-specific quality data. Enter your lot number to retrieve the exact COA.
Look up COA →Full quality attributes and acceptance criteria for this grade.
View spec sheet →Taxonomy Tree
| Kingdom | Organic compounds |
|---|---|
| Superclass | Benzenoids |
| Clase | Phenol ethers |
| Subclass | Anisoles |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Anisoles |
| Alternative Parents | Phenoxy compounds Methoxybenzenes Cyclohexanols Aralkylamines Alkyl aryl ethers Tertiary alcohols 1,3-aminoalcohols Trialkylamines Cyclic alcohols and derivatives Organopnictogen compounds Hydrocarbon derivatives |
| Molecular Framework | Aromatic homomonocyclic compounds |
| Substituents | Phenoxy compound - Anisole - Methoxybenzene - Alkyl aryl ether - Aralkylamine - Cyclohexanol - Monocyclic benzene moiety - 1,3-aminoalcohol - Tertiary alcohol - Cyclic alcohol - Tertiary aliphatic amine - Tertiary amine - Ether - Organic nitrogen compound - Organonitrogen compound - Organooxygen compound - Hydrocarbon derivative - Organopnictogen compound - Amine - Organic oxygen compound - Alcohol - Aromatic homomonocyclic compound |
| Descripción | This compound belongs to the class of organic compounds known as anisoles. These are organic compounds containing a methoxybenzene or a derivative thereof. |
| External Descriptors | tertiary alcohol - tertiary amino compound - monomethoxybenzene - cyclohexanols |
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| Índice de refracción | n20D1.54 (Predicted) |
|---|---|
| Punto de ebullición (°C) | 397.58° C at 760 mmHg (Predicted) |
| Punto de fusión (°C) | 72-74° C (lit.) |
| Peso molecular | 277.400 g/mol |
| XLogP3 | 2.900 |
| Hydrogen Bond Donor Count | 1 |
| Hydrogen Bond Acceptor Count | 3 |
| Rotatable Bond Count | 5 |
| Exact Mass | 277.204 Da |
| Monoisotopic Mass | 277.204 Da |
| Topological Polar Surface Area | 32.700 Ų |
| Heavy Atom Count | 20 |
| Formal Charge | 0 |
| Complexity | 279.000 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 1 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| The total count of all stereochemical bonds | 0 |
| Covalently-Bonded Unit Count | 1 |
| 1. Da Wang, Stefanos Giannakis, Jingyu Tang, Kai Luo, Juntao Tang, Zhiqiao He, Shuang Song, Lizhang Wang. (2023) Effect of rGO content on enhanced Photo-Fenton degradation of Venlafaxine using rGO encapsulated magnetic hexagonal FeTiO3 nanosheets. CHEMICAL ENGINEERING JOURNAL, [PMID:] [10.1016/j.cej.2023.147319] |
| 2. Boping Yu, Qi Han, Chaolin Li, Yuying Zhu, Xingliang Jin, Zhiguang Dai. (2021) Influencing factors of venlafaxine degradation at boron-doped diamond anode. Arabian Journal of Chemistry, [PMID:] [10.1016/j.arabjc.2021.103463] |
| 3. Lu Yang, Zijin Lin, Ruijing Mu, Wenhan Wu, Hao Zhi, Xiaodong Liu, Hanyu Yang, Li Liu. (2024) Neurons enhance blood–brain barrier function via upregulating claudin-5 and VE-cadherin expression due to glial cell line-derived neurotrophic factor secretion. eLife, [PMID:39475379] [10.7554/eLife.96161] |
| 4. Moying Yang, Yan Yao, Haotian Shen, Fei Teng, Yunuo Liu, Yuyang Ma, Bin Di, Mengxiang Su. (2025) Detection of antidepressants in wastewater from four provinces of China by UPLC-MS/MS to assess the regional prevalence of depression. MICROCHEMICAL JOURNAL, [PMID:] [10.1016/j.microc.2025.114446] |
| 5. Duo Xu, Bowen Du, Xuan Jiang, Jiaxin Ling, Shengwei Xiao, Huimin Sun, Xianqiang Yin. (2025) Sorption behavior of diclofenac sodium and venlafaxine on microplastics: a mechanistic study based on spectroscopy and density functional theory. Journal of Cleaner Production, [PMID:] [10.1016/j.jclepro.2025.145930] |
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