Carvedilol phosphate hemihydrate
Price 100 INR/ Kilograms
Carvedilol phosphate hemihydrate Specification
- Boiling point
- Not applicable (decomposes)
- HS Code
- 29420090
- Structural Formula
- Refer to image
- Shelf Life
- 2 years
- Poisonous
- Not classified as poisonous
- Color
- White to off-white
- Molecular Formula
- C24H27N1O4H3O4P0.5H2O
- Storage
- Store in a cool, dry, well-ventilated area away from incompatible substances
- Loss on Drying
- 0.5%
- Taste
- Bitter
- Molecular Weight
- 547.54 g/mol
- Melting Point
- 191-195C
- Solubility
- Slightly soluble in water
- Heavy Metal (%)
- 20 ppm
- Smell
- Odorless
- Medicine Name
- Carvedilol Phosphate Hemihydrate
- Chemical Name
- Carvedilol phosphate hemihydrate
- CAS No
- 125551-71-1
- Type
- Other
- Grade
- Other
- Usage
- Pharmaceutical intermediate, Antihypertensive agent, Used in treatment of heart failure and hypertension
- Purity(%)
- >=99%
- Appearance
- White to off-white powder
- Physical Form
- Powder
- Related Substances
- 0.2%
- Stability
- Stable under recommended storage conditions
- Identification
- Complies with the standard
- Packing
- HDPE drum with double lined polyethylene bags
- IUPAC Name
- 1-(Carbazol-4-yloxy)-3-[[2-(2-methoxyphenoxy)ethyl]amino]-2-propanol phosphate hemihydrate
- Microbial Limits
- Complies with pharmacopeia
- Residual Solvents
- As per ICH guidelines
Carvedilol phosphate hemihydrate Trade Information
- Minimum Order Quantity
- 1 Kilograms
- Supply Ability
- 2000 Kilograms Per Day
- Delivery Time
- 1 Days
About Carvedilol phosphate hemihydrate
Exceptional Features and Uses of Carvedilol Phosphate Hemihydrate
Carvedilol phosphate hemihydrate stands out with its outstanding purity and reliability. Its primary surface of application is pharmaceutical, primarily used as an intermediate in the manufacturing of medications to treat hypertension and heart failure. With a gilt-edged safety profileodorless, slightly soluble, and not classified as poisonousit offers flexibility for diverse pharmaceutical formulations, enhancing drug safety and performance for healthcare professionals.
FOB Port, Sample Policy, and Delivery Offers
We prioritize secure shipping through our designated FOB port, ensuring safe and efficient delivery. Take advantage of our market value pricing with an offer of structured sample policy to support your purchasing decisions. Enjoy prompt delivery times, designed to help manufacturers and traders maximize opportunities in both local and international markets. Shop now for trustworthy distribution, and benefit from our reliable export process and timely dispatch.
FAQs of Carvedilol phosphate hemihydrate:
Q: How should Carvedilol phosphate hemihydrate be stored for maximum stability?
A: It is recommended to store Carvedilol phosphate hemihydrate in a cool, dry, and well-ventilated area, away from incompatible substances. Proper storage ensures its gilt-edged stability for up to 2 years.Q: What are the main uses of Carvedilol phosphate hemihydrate?
A: Carvedilol phosphate hemihydrate is primarily used as a pharmaceutical intermediate in the production of antihypertensive agents for the treatment of heart failure and hypertension.Q: When can I expect delivery after placing an order?
A: Orders are processed promptly once confirmed, and delivery times are structured to accommodate both local and international markets through secure shipping from our designated FOB port.Q: Where can this product be applied within the pharmaceutical industry?
A: Carvedilol phosphate hemihydrate is highly recommended for application in the manufacturing of pharmaceutical formulations, especially where high purity and compliance with ICH guidelines are essential.Q: What benefits does your sample policy offer buyers?
A: Our sample policy is designed to allow buyers to evaluate product quality before committing to larger orders, supporting confident decisions at reduced market risk for manufacturers, distributors, and traders.Q: How does the product comply with regulatory standards?
A: Each batch of Carvedilol phosphate hemihydrate complies fully with pharmacopeia microbial limits, ICH guidelines for residual solvents, and strict related substance thresholds (0.2%).
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