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Moxidectin: Deep Dive into a Modern Antiparasitic

Historical Development

Decades ago, sheep and cattle producers struggled to keep roundworms at bay. Off-patent ivermectin brought help, yet resistance rose as farmers leaned hard on it. In the late 1980s, a novel class of compounds caught researchers’ attention—milbemycins. This discovery led to moxidectin’s first mention in scientific journals, sparked by fermentation work with Streptomyces cyanogriseus. Companies like American Cyanamid and later Fort Dodge farmed patents and funneled resources into wider studies, giving the world a new anthelmintic tool by the mid-1990s. Moxidectin wasn’t rushed; it went through years of trials in both animals and humans, hinting at its potential beyond just livestock. Early evidence showed longer persistence than ivermectin, which stirred hope among veterinarians and, more recently, opened doors in tackling strongyloidiasis and onchocerciasis in underserved populations.

Product Overview

Moxidectin sits in numerous livestock dewormers, equine oral gels, and pour-on solutions, not just as a singular agent but mixed in with other actives like praziquantel. Recently, oral form capsules entered human trials for river blindness in Africa, symbolizing a shift toward neglected tropical diseases. It works by binding to glutamate-gated chloride channels in nerve and muscle cells of parasites, paralyzing their bodies and flushing them from host systems. Veterinary shelves feature it under names like Cydectin, Quest, and Advocate. Each brand tailors the balance of solvents and stabilizers to its delivery style—pour-ons for cattle, gels for horses, spot-on drops for cats or dogs. The human version arrives in tablet form, standardized around purity and release profile as established by regulatory agencies.

Physical & Chemical Properties

Moxidectin’s chemical backbone, a semi-synthetic milbemycin, carries a molecular formula of C37H53NO8. Under ambient conditions, it appears as a white to pale yellow powder—virtually insoluble in water but dissolves in common organic solvents like chloroform or methanol. The structure sports a unique double bond at the 23-position, setting it apart from milbemycin D and lending it an edge in duration of action. This macrolide houses multiple hydroxyl and methoxy groups, which influence solubility profiles and drive its long persistence in biological tissues. The melting point hovers around 141‑143°C, giving formulation scientists clear cues for compounding and storability.

Technical Specifications & Labeling

Standard veterinary-grade moxidectin guarantees active content at 98% or higher, confirmed by HPLC assay. Purity caps are set by both pharmacopoeial and regulatory requirements, focusing on related substances, moisture content below 1.0%, and tight residue controls. Dosage concentrations in pour-on liquids commonly range from 0.5% to 1%; oral gels for horses reach up to 2% for single-bolus dosing. Each product label sets strict indication species, withdrawal periods—usually 14 to 28 days for meat, longer for milk—and clear user safety warnings: handlers should avoid accidental ingestion, skin exposure, or contact with eyes. Bar codes and serials on every package give traceability, aligning with global inspection guidelines.

Preparation Method

Fermentation serves as the backbone of its manufacture. Labs start with Streptomyces cyanogriseus or related strains grown in optimized media to yield milbemycin B as the initial base. Chemists then oxidize this substance at the 23-position, often using reagents like m-CPBA, before hydrating and methylating specific sites. Careful purification by column chromatography and crystallization gives the raw drug substance. Scaling up, reactors require aseptic controls to avoid cross-contamination, rigorous in-process checks for yield, and careful solvents recycling steps. In some newer workflows, manufacturers explore biocatalytic enhancements to boost yield and reduce hazardous waste.

Chemical Reactions & Modifications

Moxidectin’s chemistry revolves around modifying the milbemycin B core. Selective epoxidation at key vinyl groups and subsequent hydrolysis, followed by methylation at the lactone ring, builds the pharmacophore responsible for activity. Analytical development keeps a close eye on isomer purity and residual solvents. Derivatives get flagged in research programs, especially where longer action or increased spectrum might add value. Attempts at conjugating moxidectin with polyethylene glycol or other carriers have shown some promise in topical formulations, amplifying skin penetration or slowing release for long-acting spot-ons in companion animals.

Synonyms & Product Names

Moxidectin bears several synonyms in chemical and commercial circles. The name itself typically appears alongside international non-proprietary names. Early literature mentions it as milbemycin B, 23-(O-methyloxime), MILBEMYXIN OXIME, or 23-methoxyimino milbemycin B. Brand names scatter widely—Cydectin for livestock, Quest for equines, Advantage Multi or Advocate for canine and feline uses. Tablets under non-branded schemes for human trials simply call it moxidectin with manufacturing batch included. Cross-referencing code numbers in literature—like CP-114,935—is still common among academic teams and patent offices.

Safety & Operational Standards

Labs and farms keep strict controls when handling moxidectin, grounded in both historical incidents and regulatory lessons. The LD50 varies across species but typically sits well above field-use levels, giving some reassurance against acute harm when handlers wear gloves and use correct application devices. Environmental warnings show teeth—excess moxidectin in dung or water takes a toll on dung beetles and aquatic invertebrates. Production lines and clinics maintain chemical-resistant gloves, splash goggles, and fume extraction for bulk use. Toolkit procedures make certain that residues don’t enter feed lines or drinking water, and all surplus heads to hazardous waste channels, in line with both EPA and European REACH standards.

Application Area

Cattle, sheep, goats, horses, cats, and dogs all benefit from targeted treatments using moxidectin, especially where traditional treatments have lost punch. Vets rely on it for roundworm, lungworm, mange, and scabies infestations. It also walks into heartworm prevention for dogs and cats, often mixed with imidacloprid for dual protection. Wildlife researchers have recently used moxidectin as part of conservation programs, especially in elephants or rhinos where parasite loads undermine recovery efforts after poaching. Human clinical work remains limited, but the FDA now recognizes moxidectin for the fight against onchocerciasis—patent filings and WHO-backed programs signal hope for expanded access. Researchers in the developing world see it as a real shot at disease control in river blindness, aiming for mass drug administration as resistance to ivermectin spreads.

Research & Development

Work on moxidectin keeps breaking new ground. Resistance profiling studies directly compare it to other macrocyclic lactones, weighing its slower onset and potential as a second-line treatment. Drug delivery teams craft new depot-injection systems and nanoparticle-based carriers, focused on reducing dosing frequency for large herds or wildlife. Cross-species trials help to build broader-spectrum action against parasites—especially in emerging zoonoses. Projects supported by Gates Foundation, NIH, and EU Horizon grants now run multicenter trials, testing safety and sustained action in schoolaged children, rural workers, and military personnel stationed in endemic zones. Analytical chemists push for even lower detection thresholds in milk and meat, improving safety net for export and reducing trade rejections.

Toxicity Research

Older literature on moxidectin toxicity came mostly from rodent and ruminant work. It doesn’t cross the blood-brain barrier easily, giving mammals a margin of safety but posing real threats to breeds like collies with the MDR1 gene defect. Cases of neurotoxicity stem from overdose or accidental oral ingestion in genetically susceptible dogs—prompting genetic testing in vet clinics and robust client education. Chronic exposure studies in cattle show low tissue accumulation if withdrawal times are respected. Ecotoxicologists concerned about soil and water remote the substance’s half-life, showing persistence in dung that disrupts insect populations and aquatic food webs. Environmental monitoring and stewardship by farms and clinics set new protocols—avoiding mass application near streams and better education on safe container disposal.

Future Prospects

Moxidectin holds sway in both animal health and emerging roles in human medicine. Research partnerships with global health agencies continue shaping its place in campaigns against river blindness and strongyloidiasis. Interest grows in slow-release patches and injectable depot forms—buyers want fewer treatments and longer coverage, especially where labor or logistics lock out frequent dosing. With lessons learned on parasite resistance from older drugs, researchers push for rotation schedules and integrated parasite management plans, pairing moxidectin with biocontrol or grazing tactics. Next-generation derivatives might cut deeper into hard-to-treat nematode problems, bridging the gap for smallholder farmers in Africa or Asia, and reshaping best practices where resistance upends tradition. Regulatory green lights remain slow as agencies scrutinize both animal safety data and environmental fate, but the momentum behind global public health moves points toward a wider reach for the molecule, provided stewardship stays central and affordable generics align with ethical distribution.




What is Moxidectin used for?

A Medicine Born from Nature

Moxidectin started off in the world of veterinary care. Farmers turned to it to help sheep, cattle, and horses fight off parasites that threatened their health. This drug comes from a class called milbemycins, cousins to avermectins like ivermectin, both discovered in soil bacteria. The story—scientists sifting through dirt, searching for natural enemies of parasites—shows how sometimes the right answer comes straight from under our feet.

What Moxidectin Tackles in Animals

Worms and mites don’t get much respect, but anyone with livestock knows they can ruin a season. Moxidectin knocks back internal worms like roundworm and lungworm, but it also goes after external foes like mange mites. Parasites chew away at an animal’s health, lowering weight and milk yields. Losing a couple of sheep to worms one year makes you choose your dewormer carefully the next. Farmers choosing moxidectin often want something longer-lasting than older drugs. Studies back this up: after dosing, the protective effect in cattle lasts a few weeks longer than with ivermectin. That difference can mean one less round-up per season, which saves time and money.

The Jump to Human Medicine

In recent years, tropical medicine researchers started looking at moxidectin for people. The reason? Onchocerciasis—sometimes called river blindness—remains a scourge in parts of Africa and South America. The parasite’s worms crawl under the skin and inside the eyes, causing terrible itching and even blindness. Ivermectin has long helped, but it doesn’t kill adult worms well, so communities need repeat treatment every year, sometimes for two decades straight.

Clinical trials, published in The Lancet and other peer-reviewed journals, point out that moxidectin reduces skin parasite levels for a longer period than ivermectin. One fewer treatment per year might sound small, but in resource-poor areas, that gap can let health workers stretch their budgets. Extended time between treatments saves people from the slog and risk that comes with mass drug campaigns.

Risks and Concerns

Nothing’s perfect. Some reports describe mild side effects: itching, swelling, fatigue, headaches. For treating river blindness, dosing and monitoring must remain tight, especially because some co-infections complicate treatment. Moxidectin hasn’t reached full global approval for human use everywhere. National drug agencies consider safety data before signing off. My family has used sheep dewormers, and we've learned—never reach for a bottle before reading the label twice.

Resistance and the Search for More Tools

Parasites evolve, and resistance tends to crop up sooner or later. Overreliance on any one medicine—whether for people or livestock—can backfire. Australian cattle ranchers, for example, saw resistance to ivermectin and moxidectin after too many blanket treatments. Rotating medicines, combining drugs, and improving pasture hygiene all help.

Developing more options, investing in new molecules, and using medicines wisely could slow resistance—and protect both animals and people. This isn’t just a lab problem. On our farm, rotating paddocks and keeping a sharp eye on weak animals matters as much as choosing the right dewormer, because no drug works in a vacuum.

How is Moxidectin administered?

Understanding The Delivery

Moxidectin finds its place in the toolkit against parasitic infections in both animals and humans. People often ask about its administration, probably because getting treatment right means swifter recovery and less stress for everyone involved. For livestock and pets, moxidectin usually comes as a pour-on solution, an oral drench, injectable, or as a component in chewable tablets. Each mode brings its own set of instructions and tricks for effective use.

Taking The Guesswork Out For Farmers And Pet Owners

Hands-on experience matters when medicines are given to animals, especially in busy rural settings. In cattle ranching, the pour-on formula is common. The liquid gets measured out and applied along the back, with dosing calibrated according to body weight. Misjudging dose leads to one of two things: wasted product, or animals carrying parasites that should’ve been gone. Ranchers know that using a weigh scale or even a weight tape pays off. If you’re working with sheep or goats, oral drenches prevail. A drench gun makes things efficient, but practice saves time and fuss for the animal. Mistakes in dose calculation lead to under-treatment, resistance, or loss of stock—real risks many families can’t afford.

Giving Moxidectin To Pets

Dogs usually get moxidectin through chewable tablets or topical solutions. Veterinarians walk dog owners through applicator tips like parting fur or finding the right spot where the pet can’t lick. The message hits home: stick to the monthly cycle, or the pet loses the built-up protection. Missing these reminders happens to everyone. A little nudge from a phone alarm helps households stay on track. My own dog puts up a fuss about tablets, so I’ve learned that wrapping them in a thin piece of ham saves grief. Simpler routines reduce errors, which is why manufacturers design pills to taste better and pouches to pop open with less mess.

Human Use Calls For Extra Care

In humans, moxidectin usually comes as a single oral dose, given by a healthcare professional. Used mainly in tackling river blindness (onchocerciasis), this approach calls for basic monitoring. Swallowing the tablet with water after a meal improves absorption. For healthcare providers in low-resource settings, this tablet brings a new choice after years of relying mainly on ivermectin. Yet clarity in patient instructions is key: no splitting tablets, and no guessing at home remedies. I’ve seen confusion disappear when instructions are handed out on brightly colored cards in local languages, with stick-figure diagrams for those who share tablets among a family. Fact sheets and counseling go further than a pill alone.

Challenges And Moving Towards Smarter Use

Improper dosing and missed administrations remain huge barriers. Resistance thrives on half-measures and overuse. Up-to-date training matters as much as access itself. Sharing knowledge locally—whether it’s a demonstration day for farmers or an animal health worker’s house call—delivers more than any leaflet ever could. Moxidectin isn't magic, and follow-up matters. In every setting, tracking side effects, confirming that the medicine works in a geographic area, and rotating worm control plans stand as best practices. Solutions start with local expertise: listening to the people who administer and receive these treatments.

What Informs Responsible Moxidectin Use?

Trust grows when people can ask questions and understand the people behind the medicine. The science that drove moxidectin’s approval demanded real-world trials, clear communication, and focus on users’ needs. Every successful round of treatment traces back to the same roots: practical guidelines, training that helps people through the process, and respect for community wisdom. No one wants a treatment to fail because a step got skipped or a dose went astray. Everyone benefits when medicine goes where it’s supposed to, with hands-on knowledge lighting the way.

What are the potential side effects of Moxidectin?

Understanding Why People Care

Moxidectin often pops up in discussions about fighting parasitic infections. It originally found its place in veterinary medicine, keeping livestock free from worms that drain health and productivity. These days, doctors and global health groups also see it as a promising answer for river blindness and other neglected tropical diseases. That's a big deal if you’re living in a region where those parasites keep people from working or going to school.

Everyday Concerns: More than Just a Pill

No medication comes free of side effects, and Moxidectin is no exception. It's important for anyone considering it to understand not just statistics, but what people have really experienced. The main one to keep an eye out for is itching. As parasites start dying and leaving the body, they trigger immune responses. The kind of rash and itchiness that results can leave people uncomfortable for days or weeks. It’s not always easy to explain that this reaction, unpleasant as it is, often means the drug is working just the way it should.

Headaches and muscle aches show up sometimes—enough to keep people home from work or chores. In some cases, taking this medicine leads to dizziness or nausea. For most folks, these are temporary, but I’ve heard stories where symptoms caused enough trouble to make daily routines tough to handle. As with a lot of medicines designed to knock out pests in the body, the tougher the infection, the more intense the symptoms seem to be. Most of us would gladly trade a few uncomfortable days to be free from disease, but only if we're ready for those side effects.

Risk Factors and Real Warnings

People with weaker immune systems have more trouble shaking off side effects. In clinical studies and in my own conversations with health workers in Africa, some talk about swelling, fever, or racing heartbeats. Serious allergic reactions happen, but rarely. What’s scary is if someone already has advanced parasite infection — say, with microfilariae spread through their body — then killing off so many at once can cause reactions that need prompt medical care.

Drug interactions also factor in. Some patients on blood pressure medications or certain antidepressants face higher risk for blood pressure swings. That gets tricky in communities where medical histories often go unrecorded. Teachers and volunteers have told me about folks who don't always know their own conditions when they line up for anti-parasitic treatment campaigns. That can turn a routine dose into a safety concern.

Learning from Past Mistakes and Looking Forward

I’ve seen global health workers stress education before mass treatments. Volunteers explain not only what Moxidectin does, but what could happen in the days after taking it. Making space for people to report symptoms—even just through text messages—goes a long way toward staying ahead of complications. Nurses train others to spot warning signs and know when to step in. This trust and knowledge-building really matters; people face fewer surprises and whole communities gain confidence in new treatments.

Chasing fewer side effects comes down to sensible dosing, honest conversations about risk, and supporting people through tough hours. Doctors watch for new patterns and adjust guidelines as more real-world feedback comes in. For those battling chronic parasitic infections, understanding the ups and downs of moxidectin use can mean the difference between hope and hesitation.

Is Moxidectin safe for humans and animals?

Looking at Moxidectin’s Real World Impact

I’ve spent years working with livestock and pets, so dewormers like moxidectin have come up countless times. This drug, part of the milbemycin family, promises broad protection against a range of parasites. The conversation has grown louder now that researchers have started testing it against human parasites as well, especially where current treatments just don't work anymore.

Moxidectin for Animals: Decades of Use

Farmers rely on moxidectin to keep cattle, horses, sheep, and even dogs healthy. Used correctly, it fights everything from roundworms to mites. I’ve watched ranchers apply pour-ons or injectables with few problems. Standard side effects include some itching or swelling at the application site, but these usually clear up fast. The FDA and European Medicines Agency have both greenlit moxidectin for animal use after sifting through piles of safety data. That’s not something you see with riskier chemicals.

Misuse, especially overdosing herding dogs like collies, can bring trouble. Genetic quirks cause certain dogs to react badly to moxidectin and its cousins. Researchers from Washington State even built DNA tests to help dog owners avoid a trip to the ER. Most animals handle the medicine without drama, so it’s a favorite in shelters battling kennel cough too.

Moxidectin for Humans: Not Just a Pipe Dream

Stories out of Africa caught my attention. Some regions still struggle with river blindness, a disease that wrecks lives and ruins eyesight. Traditional treatments like ivermectin kept the problem at bay, but worm resistance meant those days wouldn’t last. Trials led by groups such as the WHO and Medicines Development for Global Health took moxidectin to the next step. Out of over 1500 people in studies, side effects were about the same or lower than current therapies: headaches, fevers, or mild skin rash. These reactions mostly linked to the body fighting off dead parasites, not the drug itself.

So far, moxidectin’s approval for humans only covers river blindness. I’ve talked to folks hoping it gets used for strongyloidiasis and scabies, where ivermectin doesn’t always finish the job. Longer-term studies show the medicine sticks around in the body for weeks, letting a single dose do the heavy lifting. Persistence could lead to wider public health campaigns reaching remote communities with fewer visits.

A Matter of Practicality and Respect

Every medicine brings risk. Moxidectin isn’t some miracle cure you pour into every feed trough or hand out without reading the label. For every animal or person helped, a handful of cases show why veterinarians and doctors take things slow. Watching for allergies, dosing by weight, and respecting withdrawal times for meat and milk keep people and food chains safe. Drug resistance looms for almost every dewormer, so we juggle moxidectin with other options, rotate formulas, and keep a close watch on the worms themselves.

Paths Toward Safer Use

People ask if moxidectin could do more for global health, especially in places with little access to basic healthcare. The tricky part lies in regulation and education. Honest communication matters: no animal medicine works as a shortcut for treating people. Updates to practice guidelines, plus more outreach in local languages, would build trust and safety. More scientists push for broader studies—on kids, pregnant women, and the elderly—since these groups often get left out of trials.

Through years in the field and at the clinic, I’ve seen moxidectin help animals thrive and humans beat stubborn diseases. There’s room for optimism, paired with a healthy respect for biology’s ability to change. Dosing smartly, following up on reactions, and teaching responsible use will shape moxidectin’s story for both animals and humans for years to come.

How does Moxidectin compare to Ivermectin?

Taking Stock of What’s on the Table

Both Moxidectin and Ivermectin have helped countless people and animals fight off parasites. Anyone familiar with veterinary care or the management of diseases like river blindness in Africa will recognize these names. Both medicines come from the same chemical family—the macrocyclic lactones. Still, the real story lies in the differences that matter in treatment and day-to-day life.

How These Drugs Pull Their Weight

I’ve watched these medicines work in livestock, and I’ve talked to doctors who prescribe them for humans. Ivermectin got its reputation for quickly knocking out parasites in humans, especially by controlling diseases like onchocerciasis (river blindness). Moxidectin, though, hasn’t been around as long for human use. It showed up in animal health first, showing promise not only because it worked, but because it stayed active longer inside the body.

That longer activity means that moxidectin can fight parasites for weeks, sometimes months, after a single dose. In real-world use, taking fewer doses saves time, money, and reduces the chance of missing treatments. Ivermectin works well, but its effects trail off sooner—so doses come closer together. For people living far from clinics or with limited access to medicine, that’s a big difference.

How Resistance Shapes the Landscape

Parasite resistance has grown into a real threat, especially in farming and places with lots of parasite transmission. Anyone running a cattle operation or health program in a tropical country can tell you—the old drugs just don’t always work. Ivermectin, with its long history, has bred resistance in some worm populations, both in animals and, more quietly, among human parasites. That’s something people living with parasites can feel right away. Moxidectin, still being relatively new, hasn’t triggered that same kind of resistance. That might be its strongest card at this point.

Safety on the Ground

Both medicines have track records that help us trust them, at least in most cases. For years, ivermectin has reached millions, with rare reports of severe side effects, usually tied to massive infection loads. I’ve listened to personal stories of relief when worms die off and symptoms fade. Moxidectin, now approved for river blindness in people, has posted similar safety results in trials. Doctors have seen how some side effects—like itching and swelling—come from the worms dying, not the drug. In animals, both drugs work safely through a range of species, giving farmers tools they can count on.

Room for Progress: Where Do We Go from Here?

Drug access is a key challenge. Ivermectin shows up thanks to donations and long distribution chains. Moxidectin still hasn’t hit that level, and many clinics can’t get their hands on it. More research on moxidectin’s long-term impact will help guide public health officials. Rural clinics and farmers need good information, too. I’ve seen how knowledge—simple facts about how and when to use each drug—makes treatments pay off, even in tough environments.

No single solution stands out yet. The fight against parasites calls for a mix of medicines, smart use, and continual research. The promise of moxidectin deserves a fair shot, especially where older treatments have lost their punch. Giving people and animals the tools to fight on their terms builds healthier communities.

Moxidectin
Names
Preferred IUPAC name (2aE,4E,8S,13S,14E,20R,21R,23S,24R)-8,23-dihydroxy-20,21,22,24-tetramethoxy-13-[(2S)-1,3-dimethylbutyl]-11,19-dimethyl-5-oxo-6,11,12,14,15,16,17,18,19,20-decahydro-2H,10H-9,4-(epoxypyrano[4,3-b][1]benzoxepin)-2a,4,8,13,14,20,21,23-octaen-2-one
Other names Cydectin
ProHeart
Quest
Advantage Multi
CYDECTIN Pour-On
CYDECTIN Injectable
CYDECTIN Oral Drench
Pronunciation /ˌmɒk.sɪˈdɛk.tɪn/
Preferred IUPAC name 4''-deoxy-4''-epi-methylaminoavermectin B1
Other names Cydectin
ProHeart
Quest
Moxidex
Advantage Multi
Afrika
Moxiclear
Pronunciation /ˌmɒk.sɪˈdɛk.tɪn/
Identifiers
CAS Number 113507-06-5
Beilstein Reference 'Beilstein Reference: 1310566'
ChEBI CHEBI:7876
ChEMBL CHEMBL525
ChemSpider 185661
DrugBank DB11748
ECHA InfoCard 03b9b895-3c36-4910-b570-639b046a2158
EC Number 2.7.1.204
Gmelin Reference 1285521
KEGG C15419
MeSH D000072680
PubChem CID 9832912
RTECS number QAN409XWZZ
UNII OWT1J78B5V
UN number UN3077
CompTox Dashboard (EPA) DTXSID2036797
CAS Number 113507-06-5
Beilstein Reference 8206564
ChEBI CHEBI:63971
ChEMBL CHEMBL1635
ChemSpider 141451
DrugBank DB11774
ECHA InfoCard 03a2ff3b-0d89-4f3b-91ad-9a42100437b8
EC Number EC 206-253-5
Gmelin Reference 144889
KEGG C08236
MeSH D000070320
PubChem CID 9832913
RTECS number QS8020000
UNII 8SK5Q7S2S4
UN number UN3077
Properties
Chemical formula C37H53NO8
Molar mass 639.832 g/mol
Appearance Light yellow crystalline powder.
Odor Odorless
Density 1.23 g/cm³
Solubility in water Insoluble in water
log P 3.6
Vapor pressure <0.0000001 mmHg (25°C)
Acidity (pKa) 10.5
Basicity (pKb) 7.6
Magnetic susceptibility (χ) -6.1·10⁻⁶ cm³/mol
Refractive index (nD) 1.63
Viscosity Viscous liquid
Dipole moment 4.49 D
Chemical formula C37H53NO8
Molar mass 639.832 g/mol
Appearance Yellow to brownish yellow powder
Odor Odorless
Density 1.04 g/cm3
Solubility in water Insoluble in water
log P 3.8
Vapor pressure <0.0000001 mm Hg (25°C)
Acidity (pKa) 4.1
Basicity (pKb) 7.1
Magnetic susceptibility (χ) -6.7e-6
Refractive index (nD) 1.63
Viscosity Viscous liquid
Dipole moment 3.73 D
Thermochemistry
Std molar entropy (S⦵298) 234.7 J·mol⁻¹·K⁻¹
Std enthalpy of combustion (ΔcH⦵298) Std enthalpy of combustion (ΔcH⦵298) of Moxidectin: **-12077 kJ/mol**
Std molar entropy (S⦵298) 303.7 J·mol⁻¹·K⁻¹
Std enthalpy of formation (ΔfH⦵298) -621.3 kJ/mol
Pharmacology
ATC code P54AA29
ATC code P02CX08
Hazards
Main hazards May be harmful if swallowed or absorbed through skin. Causes skin and eye irritation. Toxic to aquatic life with long lasting effects.
GHS labelling GHS07, GHS08
Pictograms GHS06, GHS08
Signal word Warning
Hazard statements H302, H319, H410
Precautionary statements P264, P270, P273, P280, P301+P312, P330, P391, P501
NFPA 704 (fire diamond) 1-2-0
Flash point > 203.8 °C
Lethal dose or concentration LD50 (oral, rat): >2,000 mg/kg
LD50 (median dose) LD50 (oral, rat): 86 mg/kg
NIOSH Not listed
PEL (Permissible) 0.01 mg/m³
REL (Recommended) 0.2 mg/kg
Main hazards May be harmful if swallowed; causes eye irritation; may cause allergic skin reaction; toxic to aquatic life with long lasting effects.
GHS labelling GHS07, GHS09
Pictograms GHS06, GHS08
Signal word Warning
Hazard statements H302, H410
Precautionary statements P264, P270, P273, P280, P301+P312, P330, P391, P501
Flash point > 200°C
Lethal dose or concentration LD50 (oral, rat): 86 mg/kg
LD50 (median dose) LD50 (median dose) of Moxidectin: "94 mg/kg (oral, rat)
PEL (Permissible) Not established
REL (Recommended) 0.2 mg/kg
IDLH (Immediate danger) Not Established
Related compounds
Related compounds Abamectin
Doramectin
Eprinomectin
Ivermectin
Selamectin
Related compounds Ivermectin
Abamectin
Milbemycin oxime
Selamectin
Doramectin