Azetidine hydrochloride
Based on 1 Customer Validation
Azetidine (Trimethyleneimine) hydrochloride is a four-membered saturated nitrogen-containing heterocyclic compound. Azetidine hydrochloride is often used as a building block or scaffold in chemical synthesis for the development of azetidine-based STAT3 inhibitors, GlyT1 inhibitors, and fluorophore modifiers.
For research use only. We do not sell to patients.
- Purity : 97.0%
- CAS No.: 36520-39-5
- Formula: C3H8ClN
- Molecular Weight:93.56
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Storage:
4°C, sealed storage, away from moisture
* In solvent : -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture)
To place orders, for customer services and technical support, please contact: MedChemExpress USA
Tel: 609-228-6898 E-mail: [email protected] [email protected]
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Biological Activity
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Chemical Information
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Solvent & Solubility
- Purity & Documentation
- References
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Help & FAQs
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HY-40146
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3-Fluoroazetidine hydrochlorideBiochemical Reagent -
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RRx-001Radiosensitizer/CD47 and SIRP-α Inhibitor -
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Azetidine-3-carboxylic acid -
HY-W050044R
L-Azetidine-2-carboxylic acid (Standard)Proline Analog
Biological Activity
Description
In Vitro
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
Chemical Information
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CAS No. 36520-39-5
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Appearance Solid
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Molecular Weight 93.56
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Formula C3H8ClN
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Color White to off-white
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SMILES
C1CNC1.Cl
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Synonyms
Trimethyleneimine hydrochloride
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Shipping
Room temperature in continental US; may vary elsewhere.
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Storage
4°C, sealed storage, away from moisture
* In solvent : -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture)
Solvent & Solubility
In Vitro:
DMSO : 100 mg/mL (1068.83 mM; Need ultrasonic; Hygroscopic DMSO has a significant impact on the solubility of product, please use newly opened DMSO)
Please refer to the solubility information to select the appropriate solvent. Once prepared, please aliquot and store the solution to prevent product inactivation from repeated freeze-thaw cycles.
Storage method and period of stock solution: -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture). When stored at -80°C, please use it within 6 months. When stored at -20°C, please use it within 1 month.
Please refer to the solubility information to select the appropriate solvent. Once prepared, please aliquot and store the solution to prevent product inactivation from repeated freeze-thaw cycles.
Storage method and period of stock solution: -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture). When stored at -80°C, please use it within 6 months. When stored at -20°C, please use it within 1 month.
Concentration (start) × Volume (start) = Concentration (final) × Volume (final)
In Vivo:
Select the appropriate dissolution method based on your experimental animal and administration route.
- For the following dissolution methods, please ensure to first prepare a clear stock solution using an In Vitro approach and then sequentially add co-solvents:
- To ensure reliable experimental results, the clarified stock solution can be appropriately stored based on storage conditions. As for the working solution for In Vivo experiments, it is recommended to prepare freshly and use it on the same day.
- The percentages shown for the solvents indicate their volumetric ratio in the final prepared solution. If precipitation or phase separation occurs during preparation, heat and/or sonication can be used to aid dissolution.
Add each solvent one by one: 10% DMSO 40% PEG300 5% Tween-80 45% Saline
Solubility: ≥ 2.5 mg/mL (26.72 mM); Clear solution
This protocol yields a clear solution of ≥ 2.5 mg/mL (saturation unknown).
Taking 1 mL working solution as an example, add 100 μL DMSO stock solution (25.0 mg/mL) to 400 μL PEG300, and mix evenly; then add 50 μL Tween-80 and mix evenly; then add 450 μL Saline to adjust the volume to 1 mL.
Preparation of Saline: Dissolve 0.9 g sodium chloride in ddH₂O and dilute to 100 mL to obtain a clear Saline solution.
Add each solvent one by one: 10% DMSO 90% (20% SBE-β-CD in Saline)
Solubility: ≥ 2.5 mg/mL (26.72 mM); Clear solution
This protocol yields a clear solution of ≥ 2.5 mg/mL (saturation unknown).
Taking 1 mL working solution as an example, add 100 μL DMSO stock solution (25.0 mg/mL) to 900 μL 20% SBE-β-CD in Saline, and mix evenly.
Preparation of 20% SBE-β-CD in Saline (4°C, storage for one week): 2 g SBE-β-CD powder is dissolved in 10 mL Saline, completely dissolve until clear.
In Vivo Dissolution Calculator
Please enter the basic information of animal experiments:
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Recommended: Prepare an additional quantity of animals to account for potential losses during experiments.
Please enter your animal formula composition:
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%DMSO +
Recommended: Keep the proportion of DMSO in working solution below 2% if your animal is weak.
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%+
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+%Tween-80 + +
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%Saline +
The co-solvents required include: DMSO, . All of co-solvents are available by MedChemExpress (MCE). , Tween 80. All of co-solvents are available by MedChemExpress (MCE).
Working solution concentration: 0.22 mg/mL
Method for preparing stock solution: mg drug dissolved in μL DMSO. Stock solution concentration: mg/mL. * In solvent : -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture)
1. Take μL DMSO stock solution;
2. Add μL .
μL , mix evenly;
3. Then add μL Tween 80, mix evenly;
4. Then add μL
Please ensure that the stock solution in the first step is dissolved to a clear state, and add co-solvents in sequence. You can use ultrasonic heating (ultrasonic cleaner, recommended frequency 20-40 kHz), vortexing, etc. to assist dissolution.
Purity & Documentation
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Data Sheet (275 KB)
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SDS (393 KB)
- English - EN (393 KB)
- Français - FR (393 KB)
- Deutsch - DE (393 KB)
- Norwegian - NO (393 KB)
- Español - ES (393 KB)
- Swedish - SV (393 KB)
- Italian - IT (393 KB)
- Korean - KR (393 KB)
- Portuguese - PT (393 KB)
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Handling Instructions (2659 KB)
References
[1]. Zhou J, et al. Azetidine-Containing Heterospirocycles Enhance the Performance of Fluorophores. Organic letters. 2020 Jun 05;22(11):4413-4417. [Content Brief]
[2]. Hudson AR, et al. Azetidine-based selective glycine transporter-1 (GlyT1) inhibitors with memory enhancing properties. Bioorganic & medicinal chemistry letters. 2020 Jul 15;30(14):127214. [Content Brief]
[4]. Brotherton-Pleiss C, et al. Discovery of Novel Azetidine Amides as Potent Small-Molecule STAT3 Inhibitors. Journal of medicinal chemistry. 2021 Jan 14;64(1):695-710. [Content Brief]
Complete Stock Solution Preparation Table
Please refer to the solubility information to select the appropriate solvent. Once prepared, please aliquot and store the solution to prevent product inactivation from repeated freeze-thaw cycles.
Storage method and period of stock solution: -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture). When stored at -80°C, please use it within 6 months. When stored at -20°C, please use it within 1 month.
| Optional Solvent | Concentration Solvent Mass | 1 mg | 5 mg | 10 mg | 25 mg |
|---|---|---|---|---|---|
| DMSO | 1 mM | 10.6883 mL | 53.4416 mL | 106.8833 mL | 267.2082 mL |
| 5 mM | 2.1377 mL | 10.6883 mL | 21.3767 mL | 53.4416 mL | |
| 10 mM | 1.0688 mL | 5.3442 mL | 10.6883 mL | 26.7208 mL | |
| 15 mM | 0.7126 mL | 3.5628 mL | 7.1256 mL | 17.8139 mL | |
| 20 mM | 0.5344 mL | 2.6721 mL | 5.3442 mL | 13.3604 mL | |
| 25 mM | 0.4275 mL | 2.1377 mL | 4.2753 mL | 10.6883 mL | |
| 30 mM | 0.3563 mL | 1.7814 mL | 3.5628 mL | 8.9069 mL | |
| 40 mM | 0.2672 mL | 1.3360 mL | 2.6721 mL | 6.6802 mL | |
| 50 mM | 0.2138 mL | 1.0688 mL | 2.1377 mL | 5.3442 mL | |
| 60 mM | 0.1781 mL | 0.8907 mL | 1.7814 mL | 4.4535 mL | |
| 80 mM | 0.1336 mL | 0.6680 mL | 1.3360 mL | 3.3401 mL | |
| 100 mM | 0.1069 mL | 0.5344 mL | 1.0688 mL | 2.6721 mL |
Azetidine hydrochloride Related Classifications
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