Question A 4MMC nagyméretű kristályosításának legjobb módja

Mora

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Jó estét!

Körülnéztem a fórumon, hogy mi a legjobb módja a mefedron nagyszabású kristályosításának, de sok különböző módszert találtam, sok különböző ember sok különböző véleményével. Keresem a legjobb módszert, hogy szép kristályokat kapjak. Én 2b4mp-t használok DCM oldószerrel. Minden tippet és tanácsot nagyra értékelek.

Üdvözlettel,
Mora
 

Heineken

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Mennyibe kerül az u nagyméretű skála ?
 

Mora

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Körülbelül 15 kg körüli kristályosítást kell kezdeni.
 
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Heineken

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1 nap
 

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Ranbir Singh

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Which method is this how can start powder to change brown crystel
 
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Ha van ideje, a legjobb kristályokat 30/70-es víz/alkohol oldatból kapja száraz helyiségben, 18-20 ºC-on. Ez a folyamat azonban több napot vesz igénybe. A legjobb, ha páramentesítő készüléket használunk a levegő szárításához.
Ha kevés idő áll rendelkezésre, az oldószer bepárlásához jó választás a rotációs párologtató. Válassza ki a térfogat szerint. 15 kg mefedronhoz 30 liter oldószert (víz/alkohol) használ. Tehát 10 liter vagy annál nagyobb mennyiségű oldószerhez rotációs elpárologtatóra lesz szüksége.
A gyors kristályosítás azonban mindig finom frakciót ad. A kristálynövekedés folyamata időfüggő.
 
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A kristályosítás másik módszere a kristályosító folyadék hőmérsékletének csökkentése. A hőmérséklet fokozatos csökkentése -20ºC alá szükséges a durva frakció eléréséhez.
Finom frakciót gyors fagyasztással lehet nyerni. Hűtőanyagként szárazjég (CO₂) használható.
A kristályosítás meglehetősen érzékeny folyamat. Gyakorlatra van szükség az optimális eredmények eléréséhez. Ha szüksége van a segítségemre, kérem, vegye fel velem a kapcsolatot PM-ben.
 

FQ-BB

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Your problem makes it impossible to solve your problem. What is your experimental equipment, or should I help you develop a new method?
 

FQ-BB

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100 kg class 😁 Production of pharmaceutical grade crystals.
Reagents

1. Raw materials and dosage

Reagents

2-Bromo-4-methylpropiophenone (2b4mp) Reaction starting material 110 kg Purity > 98%
Methylamine solution (40%) Methylamine aqueous solution (or hydrochloride form) 45-50 kg Maintain a moderate excess to prevent incomplete reaction
Dichloromethane (DCM) Reaction and crystallization main solvent 500-600 liters Distillation purification, drying and water removal
Acetone or isopropanol Anti-solvent (for crystallization stage) 200-300 liters Anhydrous grade is preferred
Deionized water For washing and extraction 300 liters Low ion content
Anhydrous sodium sulfate Dry organic phase 5-10 kg Industrial grade or analytical grade
Activated carbon (optional) Decolorization and removal of impurities 1-2 kg For hot filtration treatment

Equipment
Reactor (200L or larger, with stirring and condensing reflux device) Material: glass lining or stainless steel
, equipped with temperature control system, vacuum interface, nitrogen protection interface cooling circulation device (-10°C to 50°C temperature control), used to accurately control the reaction temperature and cooling crystallization process, centrifuge or Buchner filter device (industrial grade), used for solid-liquid separation, collecting crystals, vacuum dryer, temperature control range: 30-50°C, ensure low solvent residue, solvent recovery device (rotary evaporator or distillation tower)
Operation steps
Dissolve 110 kg of 2-bromo-4-methylacetophenone in 200 liters of dichloromethane (DCM), start stirring and heat to 25-30°C. , add methylamine dropwise, slowly add 45-50 kg of methylamine solution (40%), control the dripping speed, and keep the reaction temperature at 20-30°C. The temperature is critical at this stage and should not exceed 30°C to prevent side reactions. Time control: 4-6 hours, ensure uniform dropwise addition and complete reaction. Monitor the progress of the reaction to confirm that the raw materials have been basically exhausted. After the reaction is completed, let it stand and cool to 20°C, add an equal amount of **deionized water (200-300 liters)** to separate the layers. Wash with deionized water 3 times until the pH is close to neutral. Dry the organic layer with anhydrous sodium sulfate, stir for 30 minutes and filter to obtain a dry DCM solution. Heat the dry DCM solution to 40°C to ensure that the target product is completely dissolved. If the solution is dark in color, add activated carbon (1-2 kg) and stir for 30 minutes, then filter hot to remove impurities and pigments. Slowly cool to room temperature (20-25°C) and stir for 30 minutes. Continue to cool the solution to 0-5°C and keep for 1 hour. The crystals will gradually transfer the crystals to a vacuum dryer, set the temperature to 40°C, and dry for 6-8 hours until the solvent residue is less than 0.5%.

Separate and recycle the solvent

The recovered mother liquor is filtered through a coarse filter to remove solid impurities or crystal residues to prevent clogging of the distillation system. The mother liquor is poured into the distillation kettle, and the filling amount is 70-80% of the total capacity of the kettle to prevent overflow or excessive foaming. Atmospheric or reduced pressure distillation, the temperature is controlled at 40-45°C, and the pressure is set at 30-50 mbar (reduced pressure state) to prevent the decomposition of dichloromethane. The steam is cooled into liquid through the condenser and enters the receiving tank. The cooling water temperature is maintained at 0-5°C to improve the condensation efficiency. Re-distillation (optional): For solvents that are used multiple times, secondary distillation can be performed to improve the purity. The cost of recovering dichloromethane is only 10-20% of the new purchase cost. The purity of the solvent after recovery meets the requirements of reaction and crystallization

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