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Ivermectin

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Ivermectin molecular structure
Quick Facts
CAS Number70288-86-7
Molecular FormulaB1a (C48H74O14), B1b (C47H72O14)
Molecular Weight875.1
PharmacopoeiaEP/USP/IN HOUSE
Packaging25 KG/DRUM
Veterinary Grade EP/USP/IN HOUSE 25 KG/DRUM

Product Story

Ivermectin was discovered in the mid-1970s through a landmark international scientific collaboration. In 1973, Japanese microbiologist Satoshi Omura isolated a novel actinobacterium, Streptomyces avermitilis, from a soil sample collected near a golf course in Ito, Japan. Omura sent the culture to Merck Research Laboratories in the United States, where parasitologist William C. Campbell's team discovered that fermentation broths of the organism contained potent anti-parasitic macrocyclic lactones — named avermectins. Through chemical reduction, the most active derivative, 22,23-dihydroavermectin B1 (ivermectin), was developed and launched in 1981.

Ivermectin acts by selectively and irreversibly binding to glutamate-gated chloride ion channels (GluCls) in invertebrate nerve and muscle cells. This binding increases chloride ion permeability, causing hyperpolarization of the cell membrane, paralysis, and death of the parasite. Mammals lack GluCls in their peripheral nervous system (the channels are confined to the CNS, protected by the blood-brain barrier), which accounts for ivermectin's remarkable safety margin in livestock — typically >100-fold between therapeutic and toxic doses.

Ivermectin's unique advantage is its dual action as both an endectocide (killing internal nematodes) and an ectoparasiticide (killing external mites, lice, ticks). A single administration provides broad-spectrum parasite control that previously required multiple products. The discovery of avermectins (lead compound of ivermectin) earned Omura and Campbell half of the 2015 Nobel Prize in Physiology or Medicine (shared with Tu Youyou for artemisinin), with the Nobel Committee declaring that these drugs "have revolutionized the treatment of some of the most devastating parasitic diseases." Ivermectin transformed veterinary medicine — it remains the most widely used veterinary antiparasitic agent globally, with billions of doses administered across cattle, sheep, swine, horses, poultry, and companion animals.

As of mid-2026, the global veterinary ivermectin API market is driven by expanding livestock production in Asia, Latin America, and Africa, where parasite control directly impacts meat, milk, and fiber yields. Growing resistance in gastrointestinal nematodes, particularly Haemonchus contortus in small ruminants, is pushing demand toward combination products and higher-purity API. China is the dominant producer of ivermectin API, with manufacturing concentrated in Shandong and Hebei provinces. Quality differentiation — between GMP-grade and agricultural-grade material — is widening as regulatory agencies tighten antiparasitic residue monitoring in food-producing animals.

Quality Specifications

Purity (HPLC)≥ 95.0% B1a component, B1a + B1b ≥ 97.0% (anhydrous basis), per EP/USP
Component RatioB1a ≥ 90.0% (EP); B1b ≤ 5.0% (critical quality attribute for bioactivity)
Related SubstancesAny individual unspecified impurity ≤ 1.0%; total impurities ≤ 3.0% (EP)
Residual SolventsCompliant with ICH Q3C; ethanol ≤ 5,000 ppm
Heavy Metals≤ 20 ppm
GMP StatusManufactured under ICH Q7 GMP conditions
Key TestsLoss on drying ≤ 1.0%; specific optical rotation -20° to -17°; identity confirmed by IR spectrum

Veterinary Applications

Injectable & Pour-On (Cattle)

1% injectable and 0.5% pour-on formulations. Controls GI roundworms, lungworms, cattle grubs, lice, and mange mites. Standard dose: 0.2 mg/kg SC injection or 0.5 mg/kg pour-on.

Oral Drench & Paste (Sheep, Horses)

Oral drench for sheep (0.08%) at 0.2 mg/kg. Oral paste for horses (1.87%) for strongyles, ascarids, pinworms, and stomach bots. Extended protection from a single administration.

Therapeutic Areas

  • Cattle: Pour-on and injectable formulations for GI roundworms, lungworms, grubs, lice, and mites
  • Sheep & Goats: Oral deworming for Haemonchus, Ostertagia, Trichostrongylus, and nasal bots
  • Swine: Injectable and in-feed formulations for Ascaris, Hyostrongylus, and sarcoptic mange
  • Horses: Oral paste for strongyles, ascarids, pinworms, and stomach bots
  • Poultry: Mite and lice control in commercial layer and breeder operations
  • Companion Animals: Heartworm prevention in dogs (oral tablets, monthly dosing)

Sourcing Ivermectin API: Key Checks

Documentation

Request CoA with HPLC assay showing B1a/B1b component ratio, impurity profile, and residual solvent statement. Verify GMP certificate validity. For regulated markets, confirm VMF/DMF filing status and pharmacopoeia compliance (EP or USP).

Red Flags

Low B1a content (below EP limit of 90.0%), elevated degradation products indicating improper fermentation control or poor storage, pricing far below market range (suggesting non-GMP or agricultural-grade material), and refusal to share batch-specific component ratio data.

Packaging & Logistics

Standard: 25 KG/DRUM, light-resistant packaging recommended. Ivermectin is photolabile — verify aluminum foil-lined drums or opaque containers. Store at controlled room temperature (15-25 °C). Standard lead time 4-8 weeks.

Market Context

Global ivermectin API market growing at 4-6% CAGR, driven by livestock expansion in Asia-Pacific and Africa. Rising anthelmintic resistance is shifting demand toward combination products and GMP-pure API. China dominates global production (>80% of supply). Market report

Frequently Asked Questions

Ivermectin targets glutamate-gated chloride ion channels (GluCls) that are present in invertebrates but absent from the mammalian peripheral nervous system. In mammals, GluCls are confined to the central nervous system, which is protected by the blood-brain barrier and the efflux transporter P-glycoprotein (P-gp). At therapeutic doses, ivermectin is actively pumped out of the CNS by P-gp and does not reach neurotoxic concentrations. This selectivity gives ivermectin a therapeutic index exceeding 100 in most livestock species. Dogs with MDR1 gene mutations (notably Collies and related breeds) have defective P-gp and are at risk of neurotoxicity at standard doses.
Ivermectin is a mixture of two homologous compounds: B1a (C48H74O14) and B1b (C47H72O14). B1a is the major bioactive component and must account for at least 90.0% of total content per EP monograph. The B1a/B1b ratio is determined by the fermentation strain and production process — it directly correlates with antiparasitic potency. A low B1a percentage indicates either a suboptimal fermentation strain, process drift, or degradation. Reputable API suppliers report B1a and B1b content by HPLC on every batch CoA. This is the most important quality parameter for ivermectin API — more critical than total purity alone.
Widespread ivermectin resistance has emerged in gastrointestinal nematodes of small ruminants, particularly Haemonchus contortus (barber's pole worm) in sheep and goats across Africa, Asia, and Latin America. Resistance is also increasing in cattle Cooperia species. The industry response has been twofold: (1) combination anthelmintic products pairing ivermectin with a drug of a different class (e.g., closantel, levamisole) to delay resistance development; (2) stricter dosing accuracy and rotation strategies. For API buyers, this trend reinforces the importance of high-purity GMP material — underdosing due to substandard API accelerates resistance selection.
Ivermectin has established Maximum Residue Limits (MRLs) in all major markets. The Codex Alimentarius MRLs are: cattle liver 800 mcg/kg, cattle fat 400 mcg/kg, sheep/pig liver 15-30 mcg/kg. Withdrawal periods vary by species and formulation: 35-49 days for injectable cattle products, 14-28 days for pour-on formulations, and 7-14 days for oral sheep drenches. EU and US regulators conduct routine residue monitoring in imported meat. Using GMP-grade API from a certified supplier with batch-specific CoA documentation is essential for demonstrating compliance with MRL requirements and avoiding import rejections.
Standards: EP/USP/IN HOUSE  |  CAS: 70288-86-7  |  Quality data verified against pharmacopoeia monograph COA and MSDS available  |  DrugBank  |  July 2026

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