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Views: 64 Author: Site Editor Publish Time: 2023-02-10 Origin: Site
Pharmaceutical intermediates refer to a substance between the raw material drug and the final preparation, which can be converted into the final pharmaceutical preparation through drug synthesis or other methods.
These substances can be natural substances or artificially synthesized, some of which can be used as raw materials of medicines, and others can be used as active ingredients of medicines.
(1) Drug intermediates: mainly used as raw materials for the synthesis of drugs, such as amino acids, aromatics, alkanols, enols, and sugar intermediates.
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(2) Fragrance intermediates: mainly used as raw materials for the synthesis of fragrances, such as aldehydes, carboxylic acids, ketones, esters, ethers, etc.
(3) Dye intermediates: mainly used as raw materials for the synthesis of dyes, such as ketones, aldehydes, esters, carboxylic acids and amides.
(1) Hydrocarbon intermediates: mainly synthesized from hydrocarbon raw materials, such as alkanols, enols, enones, aromatics, amides, etc.
(2) Alcohol intermediates: mainly synthesized from organic alcohol raw materials, such as aldehydes, ketones, esters, ethers, etc.
(3) Acid intermediates: mainly synthesized from organic acid raw materials, such as carboxylic acids, carboxyl esters, amides, etc.
(1) Liquid intermediates: Liquid intermediates have a lower boiling point and higher solubility, such as aromatics, enols, alcohols, etc.
(2) Solid intermediates: Solid intermediates have a higher boiling point and lower solubility, such as alkanols, enones, amides, etc.
(1) Chemical synthesis intermediates: intermediates synthesized by chemical reactions, such as amino acids, enols, enones, aromatics, amides, etc.
(2) Biosynthetic intermediates: intermediates synthesized through biological reactions, such as sugars, alcohols, ketones, esters, ethers, etc.
Pharmaceutical intermediates refer to a substance that is used to convert raw materials or other intermediates to obtain final products in the process of pharmaceutical synthesis. It can transform raw materials into final products through different chemical reactions, so as to meet the requirements of pharmaceutical production. Drug intermediates have high stability and can play an important role in the process of drug synthesis.
Generally speaking, the production process of pharmaceutical intermediates includes:
1. Raw material preparation: Prepare raw materials, such as alkali, organic reagents, metal reagents, etc.;
2. Synthesis reaction: react raw materials according to the formula to obtain intermediates;
3. Washing: Wash the reaction solution to remove organic solvents and other impurities;
4. Drying: drying the washed solution to obtain the intermediate;
5. Purification: Purify the intermediate to ensure its quality;
6. Packaging: The intermediate is packaged and ready to be shipped to the customer.
The production process of pharmaceutical intermediates mainly includes synthesis, crystallization, separation, purification, stability testing, etc. Reasonable production process can improve the quality of intermediates.
The application of pharmaceutical intermediates is mainly for the synthesis of effective antibacterial drugs, antiviral drugs, anticancer drugs, anti-inflammatory drugs, antidepressant drugs, etc., as well as for the synthesis of biologically active substances and drug intermediates.
Quality control is an important part of drug quality management, and it is the same for pharmaceutical intermediates. In general, there are mainly the following control methods:
1. Raw material inspection: Before purchasing and using raw materials, the quality of raw materials should be inspected to ensure that their quality meets the requirements.
2. Standardized production: Produce in strict accordance with production standards to ensure stable product quality.
3. Process control: According to the requirements of the production process, the production process is controlled to ensure the operation specification in the production process.
4. Finished product inspection: After the production is completed, the finished product is sampled and inspected to ensure its quality meets the requirements.
5. Record management: record and save raw materials, production process, finished product inspection and other data for easy reference and review.
Nuobai Pharm, formerly the pharmaceutical division, commits to healthcare and highly focus on pharmaceuticals related business. With 30+ years of marketing intelligence in China, in combination with Nuobai Technology Ltd and GMP facility Zhejiang Langhua Pharmaceutical Co, Ltd, Nuobai Pharm provides partners with one-stop solution from development to commercialization.
Ningbo Nuobai Pharmaceutical Co., Ltd.
The Company has always been market-oriented and focused on customer satisfaction. While ensuring reliable, stable supply and cost-effective products, it strives to create value for customers by providing professional compliance solutions such as supply chain management, due diligence, third-party audit, GMP and EHS training and promotion, and drug registration at home and abroad.
Due to its high-quality products and services, the Company was selected as one of “Top 100 Pharmaceutical Internationalized Enterprises - Quality Suppliers and Partners in the International Market” by China Chamber of Commerce of Medicines & Health Products Importers & Exporters in 2019.
If you are looking for reliable pharmaceutical intermediates manufacturers and suppliers, please contact us, our professional team will provide you with high-quality services and high-quality pharmaceutical intermediates.
