129212-35-7
Tacrolimus
CAS: 129212-35-7
Molecular Formula: C44H69NO12
129212-35-7 - Names and Identifiers
129212-35-7 - Physico-chemical Properties
| Molecular Formula | C44H69NO12 |
| Molar Mass | 804.02 |
| Density | 1.19±0.1 g/cm3(Predicted) |
| Boling Point | 871.7±75.0 °C(Predicted) |
| pKa | 9.97±0.70(Predicted) |
129212-35-7 - Risk and Safety
| HS Code | 2934990002 |
129212-35-7 - Introduction
Tacrolimus EP Impurity D, also known as Impurity 1, is an impurity related to tacrolimus (Tacrolimus). Here is some information about it:
Properties: Tacrolimus EP impurity D is an organic compound, usually in solid form. Its chemical structure is similar to tacrolimus, but has different functional groups or functional groups.
Uses: Tacrolimus EP Impurity D is present as an impure of tacrolimus. In drug research and production, it is very important for the purity and quality control of drugs. Therefore, understanding and analyzing the content and nature of Tacrolimus EP impurity D is very important to ensure the safety and efficacy of the drug.
Preparation: The specific method for preparing Tacrolimus EP Impurity D may vary depending on research and manufacturing conditions. Generally, it can be obtained from tacrolimus by synthetic chemical methods, material separation or other technical means.
Safety information: Safety information regarding Tacrolimus EP impurity D may be limited because it exists primarily as an impurity of the drug. The main studies and evaluations on the safety of drugs usually focus on the main drug ingredients (such as tacrolimus). However, in the process of preparation and use, care should be taken to prevent tacrolimus EP impurity D from causing potential harm to the human body and the environment. It is essential to follow the relevant safety procedures and correct handling methods. When using drugs, follow the guidance of a doctor or professional.
Properties: Tacrolimus EP impurity D is an organic compound, usually in solid form. Its chemical structure is similar to tacrolimus, but has different functional groups or functional groups.
Uses: Tacrolimus EP Impurity D is present as an impure of tacrolimus. In drug research and production, it is very important for the purity and quality control of drugs. Therefore, understanding and analyzing the content and nature of Tacrolimus EP impurity D is very important to ensure the safety and efficacy of the drug.
Preparation: The specific method for preparing Tacrolimus EP Impurity D may vary depending on research and manufacturing conditions. Generally, it can be obtained from tacrolimus by synthetic chemical methods, material separation or other technical means.
Safety information: Safety information regarding Tacrolimus EP impurity D may be limited because it exists primarily as an impurity of the drug. The main studies and evaluations on the safety of drugs usually focus on the main drug ingredients (such as tacrolimus). However, in the process of preparation and use, care should be taken to prevent tacrolimus EP impurity D from causing potential harm to the human body and the environment. It is essential to follow the relevant safety procedures and correct handling methods. When using drugs, follow the guidance of a doctor or professional.
Last Update：2024-04-09 20:45:29
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