Methylphenidate impurity 5

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For Research Use Only | Not For Clinical Use

CAT	APB160707391
CAS	160707-39-1
Structure
Molecular Weight	218.3
Molecular Formula	C13H18N2O

What is the chemical name of CAS 160707-39-1?

The chemical name is Methylphenidate impurity 5.

What is the molecular weight of Methylphenidate impurity 5?

The molecular weight is 218.3.

What is the molecular formula of Methylphenidate impurity 5?

The molecular formula is C13H18N2O.

What is the significance of Methylphenidate impurity 5 in pharmaceuticals?

Methylphenidate impurity 5 is an impurity that may be present in pharmaceutical formulations of methylphenidate, a commonly prescribed medication for attention defic- It hyperactivity disorder (ADHD).

How is Methylphenidate impurity 5 related to the chemical structure of methylphenidate?

Methylphenidate impurity 5 is a related compound that is structurally similar to methylphenidate, but with slight variations that make it an impurity ra- Ther than the desired active ingredient.

What is the role of Methylphenidate impurity 5 in pharmaceutical quality control?

Methylphenidate impurity 5 is monitored and controlled in pharmaceutical manufacturing processes to ensure the purity and safety of the final medication.

What are the potential risks associated with the presence of Methylphenidate impurity 5 in medications?

The presence of impurities like Methylphenidate impurity 5 can impact the effectiveness, safety, and stability of medications, leading to potential health risks for patients.

How is Methylphenidate impurity 5 detected and quantified in pharmaceutical samples?

Analytical techniques such as chromatography, spectroscopy, and mass spectrometry are commonly used to detect and quantify impurities like Methylphenidate impurity 5 in pharmaceutical samples.

What are the regulatory guidelines regarding the limits of Methylphenidate impurity 5 in pharmaceutical products?

Regulatory authorities such as the FDA and EMA have established acceptable limits for impurities like Methylphenidate impurity 5 in pharmaceutical products to ensure patient safety and product quality.

How can pharmaceutical manufacturers minimize the presence of Methylphenidate impurity 5 in their products?

Manufacturers can implement strict quality control measures, conduct thorough testing of raw materials and finished products, and adhere to good manufacturing practices to minimize the presence of impurities like Methylphenidate impurity 5 in their products.

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