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Trimethoprim Powder

Trimethoprim Powder

Appearance: White to off-white powder
Specification: 98% min
CAS Number: 738-70-5
Molecular Formula: C14H18N4O3
Molecular Weight: 290.32
EINECS: 212-006-2
Shelf Life: 2 Years Proper Storage
Stock: Fresh Stock
Certificate: COA,GMP,ISO,HACCP
Service: OEM&ODM Service

Product Introduction

Trimethoprim API CAS 738-70-5 | ≥98% Antibacterial Synergist Manufacturer China

Key Selling Points

✓ Diaminopyrimidine Antibacterial - Selective Bacterial DHFR Inhibitor

✓ Gold-Standard Sulfonamide Synergist - Sequential Folate Blockade (Bactericidal)

✓ Co-Trimoxazole Partner - SMX:TMP 5:1, WHO Essential Medicine

✓ Broad Gram-Positive & Gram-Negative Spectrum - E. coli, Pasteurella, Streptococcus, Staph

✓ Excellent Oral Absorption & Tissue Distribution - Prostate, Respiratory, UTI

✓ Human & Veterinary API - UTI, Respiratory, Prostatitis, PJP Prophylaxis

 

What Is Trimethoprim Powder?

 

Trimethoprim Powder (TMP) is a synthetic diaminopyrimidine antibacterial, chemically 2,4-diamino-5-(3,4,5-trimethoxybenzyl)pyrimidine. It is best known as the diaminopyrimidine component of co-trimoxazole - the fixed 5:1 combination with sulfamethoxazole (SMX), listed on the WHO Model List of Essential Medicines - and is also paired with sulfadiazine (co-trimazine) and sulfadoxine (co-trimoxine).

 

It is used alone for uncomplicated UTI and prostatitis, and in combination with SMX for respiratory infections, traveler's diarrhea, and the prophylaxis/treatment of Pneumocystis jirovecii pneumonia (PJP), toxoplasmosis and nocardiosis. In veterinary practice it is formulated with sulfonamides for respiratory, GI and urinary infections in cattle, sheep, pigs, poultry, dogs and cats caused by susceptible organisms. Alone bacteriostatic; its value lies in selective inhibition of bacterial DHFR (~50,000-fold affinity over mammalian DHFR). Well absorbed orally, good tissue distribution (including prostate), half-life ~8–12 hours. High/prolonged doses may cause folate deficiency (manageable with folinic acid); most serious co-trimoxazole adverse effects are sulfonamide-related.

 

How Does Trimethoprim Powder Work?

 

Trimethoprim Powder selectively and reversibly inhibits bacterial dihydrofolate reductase (DHFR), blocking conversion of dihydrofolic acid (DHF) to tetrahydrofolic acid (THF) - the active folate coenzyme for purine, thymidine and amino acid synthesis. Because Trimethoprim Powder binds bacterial DHFR far more tightly than mammalian DHFR, it depletes THF selectively in microorganisms, arresting DNA replication. Alone bacteriostatic.

 

Its defining feature is synergy with sulfonamides: sulfonamides inhibit DHPS at the preceding folate step, while TMP blocks DHFR at the next - a sequential blockade that converts bacteriostasis to bactericidal activity, broadens spectrum and slows resistance. Optimal tissue ratio ~1:20 (TMP:sulfonamide), achieved with a 1:5 oral fixed dose. Active against Gram-positive (Staphylococcus, Streptococcus, Listeria) and Gram-negative (E. coli, Klebsiella, Proteus, Salmonella, Pasteurella) organisms, plus P. jirovecii and T. gondii with SMX. Renal excretion; dose adjustment in significant renal impairment.

 

What Are the Applications of Trimethoprim Powder?

 

  • Urinary Tract Infections: Uncomplicated UTI caused by susceptible E. coli and other Gram-negative uropathogens (used alone or as co-trimoxazole).
  • Respiratory Tract Infections: Acute exacerbations of chronic bronchitis, sinusitis and pneumonia, typically as co-trimoxazole or potentiated sulfonamide combinations.
  • Pneumocystis jirovecii Pneumonia (PJP): Prophylaxis and treatment in immunocompromised patients - the gold-standard indication for co-trimoxazole.
  • Veterinary Infections: Formulated with sulfonamides for bovine respiratory disease (Pasteurella, Mannheimia), swine pleuropneumonia (Actinobacillus, Streptococcus suis), poultry colibacillosis and pasteurellosis, and canine/feline UTI, skin and respiratory infections.
  • Gastrointestinal Infections: Traveler's diarrhea (ETEC), shigellosis and other susceptible bacterial enteritides.

 

What Is the Difference Between Trimethoprim and Sulfamethoxazole?

 

Feature Trimethoprim Sulfamethoxazole
CAS 738-70-5 723-46-6
Class Diaminopyrimidine Sulfonamide
Target Enzyme DHFR (dihydrofolate reductase) DHPS (dihydropteroate synthase)
Pathway Step DHF → THF PABA → DHF
Alone Bacteriostatic Bacteriostatic
Combined Sequential blockade → bactericidal Sequential blockade → bactericidal
Half-Life 8–12 hours 10–12 hours
Selective Toxicity High (bacterial DHFR) High (bacteria synthesize folate)
Primary Adverse Effect Folate deficiency (high dose) Hypersensitivity/SJS, crystalluria

 

How Does Trimethoprim Compare With Other Diaminopyrimidines?

 

Feature Trimethoprim Ormetoprim Diaveridine Pyrimethamine
CAS 738-70-5 6981-18-6 5355-16-8 58-14-0
Primary Use Human + veterinary broad Veterinary (poultry) Veterinary (poultry coccidia) Human (toxoplasma, malaria)
Typical Partner Sulfamethoxazole Sulfadimethoxine Sulfadimidine Sulfadiazine
Bacterial DHFR Selectivity High High Moderate Lower (antiprotozoal)
Half-Life 8–12 hr ~6 hr Short ~4 days (long)
PJP Activity Yes (with SMX) No No Yes (with SD)
Veterinary Use All species Poultry Poultry/coccidia Dog/cat toxoplasma

 

How Is Trimethoprim Powder Manufactured?

 

Trimethoprim Powder is manufactured through chemical synthesis involving condensation of 3,4,5-trimethoxybenzaldehyde with a guanidine/pyrimidine intermediate, followed by reduction and purification.

 

Raw Material QC → 3,4,5-Trimethoxybenzaldehyde Preparation → Condensation with 2,4-Diaminopyrimidine Intermediate → Reduction / Cyclization → Crude Trimethoprim → Purification (Recrystallization from Ethanol/Water) → Drying → Milling → Final QC → Packaging

 

HDM BIO controls key condensation, reduction and crystallization parameters to maintain consistent purity and batch quality.

 

Quality Specifications

 

Test Item Standard Typical Result
Appearance White to off-white powder Consistent
Assay (HPLC) ≥98.0% 99.0%
Identity (IR) Conforms to reference standard Confirmed
Melting Point 199–203°C 201°C
Loss on Drying ≤0.5% 0.2%
Residue on Ignition ≤0.1% Compliant
Heavy Metals ≤10 ppm Compliant
Arsenic ≤2 ppm Compliant
Related Substances Within specification Pass
Residual Solvents Within specification Pass

 

What Quality Control Tests Are Performed for Trimethoprim Powder?

 

Each batch undergoes multi-step quality control before release to verify identity, purity and physical properties.

 

Raw Material QC → In-Process Control → HPLC Assay → IR Identity Verification → Melting Point Determination → Related Substances (HPLC) → Loss on Drying → Heavy Metals → Arsenic → Residue on Ignition → Residual Solvents → Final Batch Release

 

Key evaluations include identification via infrared (IR) spectroscopy, HPLC active content assay, melting point determination, related substances analysis, loss on drying, heavy metal and arsenic limits, residue on ignition and residual solvent testing. Every commercial batch is supported by a batch-specific COA and relevant analytical documentation for incoming QC and supplier qualification.

 

What Factors Affect Trimethoprim Powder Bulk Price?

 

Trimethoprim Powder bulk pricing is driven by several key factors:

  • Synthesis Costs: Multi-step chemical synthesis including trimethoxybenzaldehyde condensation and pyrimidine cyclization directly influences manufacturing expenses.
  • Purity & Grade: Higher purity (≥99%) and pharmaceutical-grade (USP/EP) batches command premiums over standard grade.
  • Regulatory Compliance & Certification: GMP-standard API batches with DMF/CEP and consistent COA demand a higher price.
  • Order Volume: Large-scale pharmaceutical contracts receive steeper per-kilogram discounts than small-batch orders.
  • Logistics & Geography: Cool storage / light-protected packaging requirements and customs compliance add to the landed cost.

Contact HDM BIO for a current quotation and volume-based pricing.

 

Why Choose HDM BIO as Your Trimethoprim Powder Supplier?

 

  • High-purity (≥98% / typical 99%) diaminopyrimidine DHFR inhibitor with proven sulfonamide synergy
  • Gold-standard co-trimoxazole partner - 5:1 SMX:TMP, WHO Essential Medicine
  • Broad-spectrum activity with excellent oral absorption and tissue distribution (including prostate)
  • GMP-aligned production, ISO & HACCP certified quality system
  • Full batch traceability and complete documentation (COA, MSDS, HPLC)
  • Flexible supply: kilogram samples to ton-level bulk orders
  • Global export to 70+ countries with full customs support

 

Bulk Packaging, Shipping & Storage

 

  • Packaging: Foil bags for samples and moisture-proof fiber drums for bulk orders.
  • Custom Packaging: OEM labeling available.
  • Shipping Documents: COA, MSDS/SDS, commercial invoice, packing list and customs documentation available according to order requirements.
  • Storage: Store tightly sealed in a cool, dry, light-protected environment. Shelf life: 24 months.
  • Handling: For veterinary raw material use only; not for direct clinical administration.

 

Frequently Asked Questions About Trimethoprim Powder

 

Q1: What is Trimethoprim Powder?

A: A synthetic diaminopyrimidine antibacterial (TMP) that selectively inhibits bacterial dihydrofolate reductase (DHFR), best known as the partner of sulfamethoxazole in co-trimoxazole.

 

Q2: What is the CAS number?

A: 738-70-5.

 

Q3: How does trimethoprim work?

A: It reversibly inhibits bacterial DHFR, blocking conversion of DHF to THF. With sulfonamides (which inhibit DHPS at the preceding step), it creates a sequential folate pathway blockade with bactericidal synergy.

 

Q4: What is co-trimoxazole?

A: The fixed combination of trimethoprim and sulfamethoxazole in a 1:5 ratio (e.g., 80 mg/400 mg or 160 mg/800 mg), which is bactericidal and listed as a WHO Essential Medicine.

 

Q5: What is trimethoprim used for?

A: Urinary tract infections, prostatitis, respiratory infections, traveler's diarrhea, and - as co-trimoxazole - PJP prophylaxis/treatment, toxoplasmosis and nocardiosis. In veterinary: potentiated sulfonamide formulations for respiratory/GI/UTI in livestock and pets.

 

Q6: What documents are provided with each batch?

A: Batch-specific COA, HPLC report, IR identity records, melting point data, MSDS/SDS and relevant export documentation.

 

Q7: What purity do you supply?

A: Standard ≥98% HPLC; typical batch result 99%. USP/EP-grade available on request.

 

Q8: Where can I buy it from China?

A: HDM BIO supplies bulk Trimethoprim Powder with batch COA and global export support.

 

Q9: How much does Trimethoprim Powder cost?

A: Bulk pricing depends on synthesis costs, purity/grade, regulatory compliance, order volume and logistics. Contact HDM BIO for a current quotation.

 

Q10: Are there any safety concerns?

A: Trimethoprim is generally well tolerated, but high or prolonged doses may cause folate deficiency (megaloblastic anemia, leukopenia, thrombocytopenia), manageable with folinic acid. Most serious adverse effects in co-trimoxazole are attributable to the sulfonamide component. Dose adjustment required in renal impairment. Not for direct clinical administration.

 

factory

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Certificates

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trimethoprim-powder-iso-haccp-certificate.webp

Shipping & Packing

 

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Request COA, Samples & Bulk Quotation

 

  • Batch-specific COA & MSDS
  • GMP & ISO Certification
  • Custom Bulk Pricing
  • Research Samples Available

 

Contact:
Whatsapp & Mobile: +86 19991242181

Email: sales@hdmbio.com

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