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Send InquiryPamabrom .
Price 100 INR/ Kilograms
MOQ : 1 Kilograms
Pamabrom . Specification
- Particle Size
- Typically 90% <100 microns
- Taste
- Slightly bitter
- Color
- White to off-white
- Smell
- Odorless
- Poisonous
- Non-poisonous at therapeutic doses
- Solubility
- Soluble in water, slightly soluble in alcohol
- Boiling point
- Not available (decomposes before boiling)
- EINECS No
- 210-096-8
- Storage
- Store in a cool, dry place, tightly closed
- Ph Level
- 6.0 7.5 (1% solution)
- Structural Formula
- (image not displayed in text format)
- Heavy Metal (%)
- 0.001%
- HS Code
- 2921.59
- Molecular Weight
- 346.26 g/mol
- Shelf Life
- 2 years under recommended conditions
- Melting Point
- 204-206C
- Molecular Formula
- C16H20BrN3O
- Loss on Drying
- 0.5%
- Medicine Name
- Pamabrom
- Chemical Name
- 4-Bromo-2,3-dimethylaniline complex with 2-amino-2-methyl-1-propanol
- CAS No
- 606-04-2
- Type
- Other
- Grade
- Other
- Usage
- Diuretic, mainly used to relieve symptoms of premenstrual and menstrual bloating
- Purity(%)
- >98%
- Appearance
- White to off-white powder
- Physical Form
- Powder
- Packaging
- HDPE drum / Fiber drum / Customized
- Storage Temperature
- 15-30C
- Compatibility
- Compatible with most excipients
- Grade Standard
- USP / Pharmaceutical grade
- pH Value (1% solution)
- 6.0 - 7.5
- Residual Solvents
- Complies with USP/NF
- Stability
- Stable under recommended storage conditions
- Impurity Limit
- 1.0%
- Identification
- Meets USP test
Pamabrom . Trade Information
- Minimum Order Quantity
- 1 Kilograms
- Supply Ability
- 2000 Kilograms Per Day
- Delivery Time
- 1 Days
- Main Domestic Market
- All India
About Pamabrom .
Pamabrom stands as a featured and premier pharmaceutical-grade diuretic, widely recognized and sought-after in the healthcare industry. This monumental product, with over 98% purity, presents as a white to off-white powder and complies with strict USP/NF standards regarding residual solvents and heavy metals. Identification meets USP test with a structural formula of C16H20BrN3O and a pH value of 6.07.5. Stored at 1530C in HDPE or fiber drums, Pamabrom is stable and compatible with most excipients. Used to relieve premenstrual and menstrual bloating, it offers superior stability and purity for advanced therapeutic applications. Manufactured, distributed, and exported by leading suppliers in India, Pamabrom represents a special advance purchase for traders, importers, and healthcare providers.
Pamabrom: Method, Competitive Edge & Plant Application
Pamabrom is typically administered orally and exhibits rapid onset of diuretic action which supports its application in addressing fluid retention and bloating. Its monumental compatibility with most pharmaceutical excipients enables seamless plant integration and formulation. Competitive advantages include stringent impurity control (1.0%), impressive stability under recommended conditions, and USP pharmaceutical grade assurance. Distributors and manufacturers benefit from versatile packaging options, ensuring product integrity throughout the supply chain.
Pamabrom: Export Logistics & Market Insights
Pamabroms main export markets cover North America, Europe, and Asia, with strong domestic distribution throughout India. Sample policies promote expedited dispatching for authorized clients, minimizing expenditure and ensuring quality by providing representative samples before large-scale orders. Robust logistics infrastructure and advanced tracking facilitate secure and timely deliveries, aligning with trader and importer requirements for efficient supply chain operations and minimizing delays in market availability.
Pamabrom: Method, Competitive Edge & Plant Application
Pamabrom is typically administered orally and exhibits rapid onset of diuretic action which supports its application in addressing fluid retention and bloating. Its monumental compatibility with most pharmaceutical excipients enables seamless plant integration and formulation. Competitive advantages include stringent impurity control (1.0%), impressive stability under recommended conditions, and USP pharmaceutical grade assurance. Distributors and manufacturers benefit from versatile packaging options, ensuring product integrity throughout the supply chain.
Pamabrom: Export Logistics & Market Insights
Pamabroms main export markets cover North America, Europe, and Asia, with strong domestic distribution throughout India. Sample policies promote expedited dispatching for authorized clients, minimizing expenditure and ensuring quality by providing representative samples before large-scale orders. Robust logistics infrastructure and advanced tracking facilitate secure and timely deliveries, aligning with trader and importer requirements for efficient supply chain operations and minimizing delays in market availability.
FAQs of Pamabrom .:
Q: How should Pamabrom be stored to maintain optimal stability?
A: Pamabrom should be stored in a cool, dry place with the container tightly closed, ideally at temperatures between 1530C, which preserves its stability and efficacy for up to two years.Q: What is the main usage of Pamabrom in pharmaceutical applications?
A: Pamabrom is mainly used as a diuretic to relieve symptoms of premenstrual and menstrual bloating, providing rapid relief from fluid retention.Q: When should distributors request a sample of Pamabrom?
A: Distributors are encouraged to request a sample during the advance purchase process to minimize expenditure and verify product quality prior to committing to large-scale orders.Q: Where is Pamabrom primarily manufactured and exported from?
A: Pamabrom is primarily manufactured and exported by leading pharmaceutical suppliers based in India, catering to both domestic and international markets.Q: What are the benefits of Pamabroms packaging options?
A: Pamabrom offers packaging in HDPE or fiber drums, as well as customized solutions, ensuring safe storage and easy handling without compromising product stability during logistics and dispatching.Q: How does Pamabrom comply with pharmaceutical grade standards?
A: Pamabrom meets USP pharmaceutical grade standards with impurity limits 1.0%, residual solvents compliance, and compatibility with most excipients, ensuring sought-after purity and performance in formulations.
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