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Send InquiryIguratimod
Price 100 INR/ Kilograms
MOQ : 1 Kilograms
Iguratimod Specification
- EINECS No
- None assigned
- Poisonous
- No (Non-toxic at therapeutic dose)
- Smell
- Odorless
- Melting Point
- 242 - 246C
- Storage
- Store in a cool, dry place, protected from light
- Particle Size
- 90% pass through 80 mesh
- Structural Formula
- C14H13N5O2S (refer to image for structure)
- Shelf Life
- 2 years under recommended storage
- Solubility
- Slightly soluble in methanol, practically insoluble in water
- HS Code
- 29349900
- Color
- Yellow to light yellow
- Molecular Formula
- C14H13N5O2S
- Molecular Weight
- 315.35 g/mol
- Heavy Metal (%)
- 0.001%
- Loss on Drying
- 1.0%
- Medicine Name
- Iguratimod
- Chemical Name
- Iguratimod
- CAS No
- 123663-49-0
- Type
- Other
- Grade
- Other
- Usage
- Used to treat rheumatoid arthritis and autoimmune diseases
- Purity(%)
- >= 99.0%
- Appearance
- Yellow to light yellow crystalline powder
- Physical Form
- Solid
- Impurity Level
- Single impurity 0.2%, total impurities 0.5%
- Transport
- Not regulated as dangerous goods
- Identification
- By IR and HPLC meets standard
- Residual Solvent
- Within ICH limits
- Toxicological Data
- Acute oral LD50 (rat): > 5000 mg/kg
- MOQ
- 1 kg
- Packaging
- Packed in sealed HDPE drum or double polyethylene bags
- Usage Formulation
- Mainly supplied for tablet/capsule formulation
- Assay (HPLC)
- >= 99%
Iguratimod Trade Information
- Minimum Order Quantity
- 1 Kilograms
- Supply Ability
- 2000 Kilograms Per Day
- Delivery Time
- 1 Days
About Iguratimod
Iguratimod, a superlative pharmaceutical compound, is widely procured by global distributors, manufacturers, and importers seeking rarefied quality standards. Favorable reviews highlight its monumental efficacy in treating rheumatoid arthritis and autoimmune diseases. Identification is confirmed by IR and HPLC, with purity meeting or exceeding 99% (HPLC assay). Impurities are stringently controlled-single impurity 0.2%, total 0.5%. Securely featured in sealed HDPE drums or double polyethylene bags, it remains stable (shelf life: 2 years, proper storage). Its solid, odorless, yellow crystalline form is ideal for tablet and capsule formulations. Non-toxic at therapeutic dose, transport is not regulated as dangerous goods. MOQ: 1 kg.
Applications & Usage of Iguratimod
Iguratimod is primarily utilized in the formulation of tablets and capsules for the treatment of rheumatoid arthritis and related autoimmune disorders. Its application spans pharmaceutical production facilities and research laboratories focused on anti-inflammatory therapeutics. The medicine's efficacy is showcased on the surface of finished dosage forms, where its rarefied quality is maintained. Pharmaceutical companies benefit from its reliable performance in clinical and commercial environments, ensuring therapeutic consistency and patient safety.
Certifications, Supply Ability & Sample Policy for Iguratimod
Iguratimod is supplied with comprehensive certification, including detailed COA and compliance with industry standards. Stock is ready for immediate procurement, ensuring expedient packing and dispatch. Customers can estimate delivery schedules upon request. Bulk orders are filled consistently, reflecting robust supply capacity. Samples may be made available for evaluation under a defined sample policy, supporting streamlined qualification and procurement processes for distributors, importers, and pharmaceutical manufacturers alike.
Applications & Usage of Iguratimod
Iguratimod is primarily utilized in the formulation of tablets and capsules for the treatment of rheumatoid arthritis and related autoimmune disorders. Its application spans pharmaceutical production facilities and research laboratories focused on anti-inflammatory therapeutics. The medicine's efficacy is showcased on the surface of finished dosage forms, where its rarefied quality is maintained. Pharmaceutical companies benefit from its reliable performance in clinical and commercial environments, ensuring therapeutic consistency and patient safety.
Certifications, Supply Ability & Sample Policy for Iguratimod
Iguratimod is supplied with comprehensive certification, including detailed COA and compliance with industry standards. Stock is ready for immediate procurement, ensuring expedient packing and dispatch. Customers can estimate delivery schedules upon request. Bulk orders are filled consistently, reflecting robust supply capacity. Samples may be made available for evaluation under a defined sample policy, supporting streamlined qualification and procurement processes for distributors, importers, and pharmaceutical manufacturers alike.
FAQ's of Iguratimod:
Q: How is the quality of Iguratimod verified before procurement?
A: Iguratimod's quality is verified by IR and HPLC methods, ensuring it meets established identification and purity criteria. Each batch comes with a Certificate of Analysis confirming >=99% assay, low impurity levels, and compliance with regulatory standards.Q: What are the primary uses of Iguratimod in medicine?
A: Iguratimod is primarily used in the management of rheumatoid arthritis and autoimmune diseases. It is formulated into tablets and capsules, offering a reliable therapeutic solution in clinical settings.Q: Where can Iguratimod be applied in the pharmaceutical industry?
A: Iguratimod is applied in pharmaceutical manufacturing plants for the creation of oral solid dosage forms, especially in tablet and capsule production targeted at anti-inflammatory and autoimmune therapies.Q: When can buyers expect dispatch after placing an order for Iguratimod?
A: Iguratimod is kept in stock for ready packing and dispatch. Delivery timelines can be estimated based on the order quantity and destination, with prompt shipment supported for standard MOQ of 1 kg.Q: What are the transportation and storage requirements for Iguratimod?
A: Iguratimod does not require regulated transportation as it is not classified as dangerous goods. For storage, it should be kept in a cool, dry place protected from light to preserve its 2-year shelf life and superlative quality.Q: What makes Iguratimod suitable for pharmaceutical formulation?
A: Its high purity (>=99%), low impurity levels, and stable physical properties make Iguratimod ideal for pharmaceutical formulations. Its non-toxic profile at therapeutic dosage ensures safe incorporation into oral medications.
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