Question Labākais veids, kā kristalizēt 4MMC lielā mērogā

Mora

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Gudrība,

Esmu meklējis forumā labāko veidu, kā izkristalizēt mefedronu plašā mērogā, bet esmu atradis daudz dažādu metožu ar daudz dažādu cilvēku atšķirīgiem viedokļiem. Es meklēju labāko veidu, kā iegūt skaistus kristālus. Es izmantoju 2b4mp ar DCM kā šķīdinātāju. Visus padomus un ieteikumus ļoti novērtēšu.

Mīļie sveicieni,
Mora
 

Heineken

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cik daudz u ir liels mērogs ?
 

Mora

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Nepieciešams kristalizēt aptuveni 15 kg, lai sāktu ar
 
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Heineken

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1 diena
 

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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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Ja jums ir laiks, labākos kristālus iegūst no 30/70 ūdens/spirta šķīduma sausā telpā 18-20ºC temperatūrā. Taču šis process aizņems vairākas dienas. Vislabāk ir izmantot gaisa sausinātāju, lai izžāvētu gaisu.
Ja jums ir ierobežots laiks, šķīdinātāja iztvaicēšanai labi noderēs rotācijas iztvaicētājs. Izvēlieties to atkarībā no tilpuma. 15 kg mefedrona iztvaicēšanai izmanto 30 litrus šķīdinātāja (ūdens/spirts). Tātad jums būs nepieciešams rotācijas iztvaicētājs 10 litriem vai vairāk.
Bet ātra kristalizācija vienmēr dos smalku frakciju. Kristālu augšanas process ir atkarīgs no laika.
 
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Heineken

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Var darīt, bet nav nepieciešams
 
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Vēl viena kristalizācijas metode ir kristalizācijas šķidruma temperatūras pazemināšana. Lai iegūtu rupju frakciju, ir nepieciešama pakāpeniska temperatūras pazemināšana līdz temperatūrai, kas ir zemāka par -20ºC.
Smalku frakciju var iegūt, strauji sasaldējot. Kā aukstumaģentu var izmantot sauso ledu (CO₂).
Kristalizācija ir diezgan jutīgs process. Lai iegūtu optimālus rezultātus, nepieciešama prakse. Ja jums vajadzīga mana palīdzība, lūdzu, sazinieties ar mani, izmantojot PM.
 

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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