People have worked with hemin for well over a century, ever since the chemist Ludwik Niemann first recognized its crystal form in the mid-1800s. Early on, folks noticed how a drop of blood, when exposed to glacial acetic acid and a halide salt, would leave behind sparkling, dark-red crystals—the hallmark of hemin, also called hematin chloride. Early forensic science adopted this test to confirm the presence of blood at crime scenes. Over generations, the scientific community explored its structure and learned about its connection with heme, paving the way for its application not just in forensics, but in medicine, biochemistry, and industry. Scientists managed to unlock the iron-porphyrin backbone and chart how its chemistry underpins biological processes, climactically giving rise to breakthroughs in understanding hemoglobin and oxygen transport.
Hemin shows up as a deep maroon, nearly black, crystalline solid. To the scientific eye, its characteristic hue makes it easy to recognize and differentiate from other iron-based compounds. On the shelf, it remains stable when stored in a dry, cool place. While many might encounter it in the laboratory, hemin has carved out space in diagnostic kits, research reagents, pharmaceutical agents, and even as a reference standard for various biochemical assays. One can usually buy it in sealed vials, ready for weighing, dilution, and further application.
Holding hemin, you notice its brittle crystals. It fails to dissolve easily in pure water, but manages some solubility in alkaline solutions and certain organic solvents. The compound sports a molecular formula of C34H32ClFeN4O4, weighing in at around 651.94 g/mol. Its melting point tops 300°C, and it won't even budge before reaching those temperatures. The iron atom in the middle gives it a magnetic property, and the porphyrin ring structure helps it participate in key chemical and biological interactions, especially those involving oxygen and nitrogen species.
Buyers expect each shipment of hemin to meet strict criteria for chemical purity, particle size, and contamination profile. The label must declare its chemical name, batch number, purity level, and intended use. Reliable suppliers include documentation about moisture content, heavy metal traces (especially mercury and lead), and leftover solvents from synthesis. Most responsible manufacturers go further, providing certificates of analysis, safety data sheets, and clear hazard labeling, because mishandling even a low-toxicity material like hemin raises health and environmental concerns down the line.
Classic hemin synthesis follows an old recipe. Extractors boil red blood cells in glacial acetic acid, toss in sodium chloride, and watch the maroon crystals fall out as the solution cools. Modern commercialization often runs this procedure on a larger scale, using blood from livestock slaughterhouses as a starting material. After filtering and washing, the crude crystals go through multiple purifications: extractions using alcohol, solvents, and sometimes chromatographic columns. Researchers exploring synthetic porphyrins run complex multi-step organic syntheses, but for production-scale hemin, the blood-based route still dominates, mainly because nothing else matches in cost or yield.
Hemin’s iron center invites oxidation and reduction reactions, trading its ferric state for a ferrous one if the right agent comes around. The porphyrin ring also opens doors to substitutions, making it possible to study analogs and learn about heme-like compounds’ behavior. Reactions can introduce other ligands or even modify the molecule’s side chains to create derivatives. People use these modified forms to test enzymes or develop probes for spectroscopic studies. In the biological world, hemin participates directly in catalytic cycles, ROS generation, and electron transport, which helps explain why it’s both a curiosity for chemists and a staple for biologists chasing down mechanisms of disease.
Different sources might call hemin by several names—chlorid hemin, hematin chloride, heme chloride, or even ferriprotoporphyrin IX chloride. Pharmaceuticals list it under branded names, such as Panhematin in the United States, or Hematin. Catalogs reference it by its registry numbers and synonyms, which helps standardize communication across jurisdictions and industries. Despite the variety in naming, the underlying structure stays the same, so once you’ve worked with hemin, it’s impossible to mistake it for another compound.
Making, handling, and using hemin requires common-sense lab practices—gloves, dust masks, chemical goggles, good ventilation. Accidentally inhaling dust or getting it in your eyes brings irritation and discomfort, so minimizing exposure always matters. Handling large amounts deserves respect for that reason. Disposal means treating it as hazardous waste, as required by local chemical safety guidelines, largely to avoid letting iron and porphyrin compounds enter groundwater or the municipal waste stream. Cleanups require a wet mop, not a broom, to keep particles out of the air. Any pharmaceutical use brings extra standards for purity, sterility, and trace contaminants.
Forensic scientists run blood confirmation tests with hemin because its crystal structure proves the sample started as blood. Beyond forensics, clinical labs sometimes use the compound for porphyria treatment, since it helps reduce toxic porphyrin buildup during acute attacks. Biochemists depend on hemin to induce heme oxygenase-1 or study cytochrome enzymes, trying to untangle oxidative stress responses or drug metabolism. The pigment also finds a home as a catalyst in organic reactions and as a standard in spectroscopic calibration. Across these applications, the precise impact of hemin often depends on the skill and curiosity of the people working with it.
Active research circles around using hemin to understand oxidative injury, inflammation, and neural degeneration. Some projects look for ways to harness hemin’s chemical tendencies for biosensor development, using it as a catalytic core for colorimetric or electrochemical devices. Others push to develop synthetic hemin analogs with fine-tuned properties, aiming for more effective pharmaceuticals or probes. Big investments go into mapping out how hemin interacts with other biomolecules, looking for clues about iron metabolism, oxidative defense, and cellular signaling. These studies bring more than academic value—they lay the groundwork for real advances in medicine and diagnostics.
Laboratory data show that hemin, though essential in small doses, brings trouble at high concentrations. Exposure through ingestion or injection in animals causes liver stress, kidney injury, and potential blood disorders, which led health authorities to label its use as risky outside medical supervision. Some studies link excess hemin with cell death through oxidative pathways and iron overload, so dosing regimens in therapeutic scenarios come under careful regulation. In environmental settings, the risk decreases, but workplace controls still keep exposures well below problematic thresholds. Toxicologists frequently revisit old data, bringing new analytical tools to make sure long-term handling recommendations stay sharp, especially as applications expand beyond the medical field.
Ongoing progress in synthetic biology puts hemin under the spotlight, promising engineered enzymes based on its porphyrin core for sustainable chemistry solutions. Drug developers look to its analogs for new treatments of blood diseases and metabolic disorders. The forensics community continues to digitize and miniaturize hemin-based assays for crime scene kits, banking on portable analysis and faster results. Scientists in advanced materials pursue hemin as a building block for electrochemical devices or bioinspired sensors. Market demand looks steady, with periodic spikes depending on the pace of pharmaceutical innovation. Hemin’s role as both a research platform and a therapeutic product ensures decades of technical challenges—exactly the kind that push researchers to keep asking what iron-centered chemistry might unlock next.
Hemin, a substance that comes from hemoglobin, doesn’t grab headlines like some other medical breakthroughs, but it quietly plays a big role in treating a rare and dangerous illness called acute intermittent porphyria (AIP). People who deal with AIP often face sudden attacks of severe belly pain, muscle weakness, and confusion. Before hemin, hospital trips felt just like a waiting game, hoping symptoms would subside. With the right treatment, these attacks can calm down much faster.
Doctors count on hemin to stop attacks before they spiral out of control. It works because it tells the body to slow down the enzymes that normally keep making certain chemicals. In people with AIP, these chemicals build up to toxic levels. Hemin helps restore the natural balance. Many people living with this disease know the feeling of getting worse in a matter of hours, but those who have received hemin can share stories of relief arriving much quicker than before.
FDA approval backs up its safety when prescribed by a physician, and hospitals keep hemin on hand for emergencies. Without this option, patients face longer and more painful hospital stays, losing weeks to recovery. It stands as a reminder that rare diseases deserve real treatment options, not just hope.
Beyond hospitals, researchers value hemin as a chemical tool. It gives insight into how blood proteins interact with oxygen and other molecules. Younger scientists might use it in class to see how iron-containing compounds react in lab tests. Its ability to change color during reactions makes lessons about biochemistry more hands-on. Over the years, countless lab reports have included hemin, helping new doctors and scientists build their knowledge at the bench rather than just the textbook.
Hemin has even helped move science forward in ways that influence blood testing and drug discovery. Studying its structure revealed details about how heme-based proteins work, which in turn has shaped the design of medicines for heart disease, anemia, and even cancer. The learning that comes from these experiments doesn’t sit on a shelf, it often leads to better diagnostic tools or new treatments for different conditions.
Even though it’s a lifeline for some, hemin costs a lot to make and distribute. Many insurance companies recognize its importance, but coverage can vary. Some patients experience delays because of price disputes or shipping setbacks. AIP attacks happen without warning—so making sure hemin is always available could mean new policies or more investment in emergency supplies. Specialty pharmacies do much of the heavy lifting by working closely with hospitals, but the supply chain could use more support to avoid any weak links.
Doctors have long asked for easier access to treatments for rare diseases. Investment in public education would help more people recognize the signs of porphyria, since fast recognition usually brings better outcomes. Hospitals in rural areas could work with larger centers to share stock, bridging gaps for patients far from urban care. Pharmaceutical companies might look at ways to cut production costs, and regulators could fast-track programs focused on rare conditions needing better logistics.
Strong advocacy from patient groups and support from the medical community can make sure that medicines like hemin do not sit out of reach for those who need them most. Stories from people who’ve recovered with this treatment highlight just how vital it is to keep working for better access, affordability, and innovation.
I’ve noticed that many folks don’t hear much about hemin unless they or someone close to them has a tough-to-treat blood condition. Hemin treatment usually comes up for people dealing with acute attacks of porphyria, a group of inherited disorders that mess with how the body makes heme—the vital molecule in red blood cells. Living with these attacks, I’ve seen, can turn life upside down: searing stomach pain, confusion, and nerve trouble pop up out of nowhere. These symptoms don’t just slow someone down for a day; they can push hospital teams into action.
Doctors don’t just hand out hemin in pill bottles. It arrives as a dark, powdered drug—packed in a glass vial, sealed for safety. Nurses get busy reconstituting this powder into a solution with sterile water. The steps matter: too much shaking or the wrong tools can wreck the medicine before it’s even in the line.
Here’s where personal experience comes in: anyone who has received intravenous infusions knows how picky veins can be. Hemin gets injected right into the bloodstream, through a vein in the arm or sometimes through a central line if regular access proves tricky. No shortcuts. Pushing the dose too quickly or missing the vein risks pain, swelling, or complications such as phlebitis (that’s irritation in the vein). I’ve watched nurses test the line first, checking for a smooth flow—never skip this check, as blood clots or infiltration can spell big trouble.
Most people notice that hospital staff with steady hands make these infusions look simple. The reality feels different for the patient. Hemin infusions can take up to half an hour, drip by drip. If air sneaks into the tube or the infusion runs too fast, side effects show up—fevers, chills, or flushing. I’ve heard patients grumble about metallic tastes during the process, which is something nurses always warn about beforehand. Everyone wants the best outcome, so the team often keeps an eye on the site and logs the time carefully.
It’s not enough to just get the drug in. Good hydration helps clear the medication and prevent kidney problems. Doctors often order plenty of fluids before and after the medicine goes in. Blood tests come with the territory, especially if treatments get repeated—liver enzymes and iron balance can shift, and those numbers steer doctors in adjusting future doses.
Some barriers still get in the way. Insurance restrictions slow access for those in need, even in severe cases. Pharmacies sometimes struggle to keep hemin stocked, given the rare use and careful handling it requires. I see hope in new delivery systems—ready-to-use preparations, less irritating formulas, maybe even oral options someday. At the same time, better nurse training and equipment could limit vein troubles and shorten hospital stays.
Listening to those who live with porphyria remains crucial, not just for comfort but for safety. Sharing tips—like warming the arm before infusion, or tucking a stress ball in your hand—makes a difference in the real world. Staying open to feedback and new ways of giving hemin could mean fewer side effects and better outcomes. In a world where rare diseases often sit in the shadows, how we give medicines like hemin shapes not just a hospital visit, but someone’s chance for a steadier life.
Hemin has helped many people manage acute porphyrias, rare genetic disorders that disrupt pathways for making heme, a crucial part of hemoglobin. Doctors prescribe it to reduce the crippling abdominal pain, vomiting, and neurological symptoms these patients often face during an attack. The drug comes with real gratitude attached for those whose lives change for the better. That said, the effects don’t always end at symptom relief. Many patients know the double-edged sword of powerful treatments. It’s useful for patients and families to know what to watch for, and for doctors to weigh the right choice for each situation.
The immediate side effects can start as soon as the drug enters the vein. Some people report warmth or redness at the injection site. There’s swelling or even dark lines—called phlebitis—if the medicine irritates the blood vessels. Nurses who infuse hemin regularly learn to flush lines with care and watch for inflammation. In rare cases, patients get skin rashes or a mild fever. These aren’t always dangerous, but they can make people feel uneasy, especially those getting the drug for the first time.
Some side effects dig deeper. Doctors warn about iron overload because hemin contains iron. Over several infusions, iron can build up in the body. That’s rough on the liver and heart. Some patients with other liver complications already brewing must be especially cautious. Permanent skin discoloration can also develop at the site if there are repeated infusions, which isn’t just a cosmetic problem for people already wrestling with a chronic disorder. Some folks have even dealt with blood clots in the vein. It’s not common, but it’s real—with a risk of longer-term issues in blood flow through the arms or legs.
People living with severe diseases often talk about the mental load of new side effects almost as much as the physical ones. The risk of allergic reactions adds one more layer of worry before each infusion. Dizziness, headache, and nausea might force someone to pause work or daily errands. These hiccups—minor to some people—can tip the scales for someone who already feels like their days revolve around managing health. That’s a unique burden those outside these experiences don’t always realize.
A practical solution starts with careful monitoring. Blood tests to check iron and liver levels become a trend in every medical chart. Having skilled nurses who know how to rotate infusion spots and check for signs of vein problems cuts down on some local irritation and clots. Some centers use central lines in patients who need repeated doses, and those who ask about home infusions get training to spot warning signs right away. Families and patients who keep written notes on symptoms make it easier for doctors to see patterns over time and adjust plans before small issues grow.
Years spent in the hospital as a volunteer, listening to patients trade stories, taught me that people just want their doctors to be straight with them. They appreciate providers who go over possible side effects, not just recite information from a pamphlet. Real trust builds up when there's a back-and-forth: shared decisions, clear explanations, options for support, and respect for what the patient already knows about their own body. Hemin won’t work for every episode or every patient, and some people do fine with very few side effects, but being heard and informed gives anyone taking it their best shot at a safer infusion and a better outcome.
Most people have never heard of hemin unless a rare medical condition enters the conversation. Doctors prescribe hemin for people with acute porphyrias, some uncommon disorders causing severe abdominal pain, mental changes, and muscle weakness. This isn’t a run-of-the-mill prescription—it’s reserved for cases where the body can’t make heme right, leading to buildup of toxic chemicals. For someone in the middle of a porphyria attack, the relief from hemin can mean the world; I’ve met a patient whose life turned a corner with access to the right treatment. Hemin helps by supplying what the body isn’t making, dialing down symptoms before they spiral out of control. So the drug matters, especially for people whose lives depend on it staying accessible—and safe—for every situation, including pregnancy.
Pregnancy throws a wrench into medical decisions for all sorts of treatments, but rare drugs like hemin draw little attention and even less long-term research. To date, human studies on hemin use in pregnancy look pretty thin on the ground. Dozens of research papers cite case reports and expert opinions more than randomized trials. Animal studies at high doses have shown some problems, mostly with the liver, but it’s never straightforward to connect animal results to people—especially pregnant people. No study has delivered a clear message that hemin causes birth defects or pregnancy loss, but “we don’t know for sure” lingers in the conversation. The U.S. FDA puts hemin in Category C, meaning risk can’t be ruled out, but potential benefits may justify its use if the mother has a real medical need. For someone in the middle of a porphyria crisis, the immediate dangers to mother and fetus often outweigh unclear risks from the medicine itself.
I once saw a hematologist facing this precise scenario. The woman in front of him, pregnant and shaking, struggled through another porphyria attack. Watching a family weigh the risks, I realized how every decision in medicine asks for more than just study results—it asks for honesty about what is known, what is unknown, and which risks matter most. In cases like hers, the consequences of not treating severe porphyria weigh heavier: seizures, high blood pressure, acute liver damage, even losing the pregnancy entirely. When you think through these dangers, it’s easy to see why expert guidelines from bodies like the American College of Obstetricians and Gynecologists and rare disease networks recommend hemin when nothing else does the job. Most stories published so far, including a summary by the European Medicines Agency, suggest that people who had to take hemin during pregnancy usually went on to deliver healthy babies.
Doctors and patients deserve clarity, not guesswork. In hospital meetings, researchers say the same thing: rare diseases almost never get the clinical trials they need. One answer sits in building better pregnancy registries, following women who use medicines like hemin and tracking what happens to their children years down the line. Clear communication in prenatal care should go hand-in-hand with the latest independent data. For anyone worried about taking a rarely used drug during pregnancy, connecting with high-risk obstetricians and rare disease specialists often means more than scouring websites. Nothing replaces the experience of a medical team that’s seen these cases before. Drug safety isn’t about ticking boxes; it’s about real people, real risks, and making the best choices possible with what’s on hand—while always pushing for better evidence.
Hemin comes from a group of molecules called heme. You’ll find heme in hemoglobin, the molecule that lets red blood cells move oxygen around the body. Hemin looks almost like heme except for an extra charge and a chloride ion. This small difference is enough for doctors to use hemin as a medicine, especially for people with acute porphyrias—a rare set of disorders that mess with the body’s ability to make heme properly.
Acute porphyrias show up when the body can’t finish building heme, causing toxic precursors to build up, mainly affecting nerves and the liver. For families who’ve seen loved ones rushed to the hospital, the pain and confusion can feel overwhelming. Muscle weakness, belly cramps, dark urine—these can all point to a porphyria attack. Hemin steps in to calm the chaos.
Picture the heme-making line in the liver as a factory. When a bottleneck pops up partway down the line, toxic products spill over into the bloodstream. Hemin acts like an outside supervisor, signaling the workers (enzymes) to slow down and stop creating waste. It feeds back to the early steps in heme synthesis, telling the main enzyme, ALAS1, to take a break. This halts the chain reaction before it reaches the toxic stage.
Over the years, I’ve seen families struggle with rare genetic disorders, feeling lost in a sea of medical jargon and repeated hospital visits. The introduction of hemin changes the narrative. Instead of treating seizures or pain alone, doctors block the toxic buildup at its root. When administered early, hemin shortens the length and severity of attacks, gets patients out of bed sooner, and sometimes lets them return to normal life quicker. For physicians, it transforms a guessing game into a straightforward protocol, giving hope to both patients and healthcare teams.
No medicine solves everything. Hemin sometimes causes iron overload, because it contains iron in its structure. Over time, too much iron can damage organs. Patients need regular monitoring of liver health, iron levels, and signs of infection from repeated infusions. Early education about symptoms helps prevent full-blown crises. Family members learn to watch for warning signs, catching flare-ups before serious nerve or liver damage happens. Peer-reviewed research has tracked outcomes over decades and found that rapid treatment with hemin improves quality of life and lowers hospital stays.
Researchers keep searching for new ways to block attacks, like RNA-based therapies or gene editing. But for now, hemin offers a proven way to control acute porphyria attacks. Reimbursement issues and shortages still pop up, especially outside big medical centers. Advocacy groups continue to speak up—giving a voice to rare disease families and making sure treatments stay both accessible and safe.
Every hospital I’ve walked into reminds me that clear information and fast action matter most for rare diseases. Hemin, born from our understanding of the body’s own chemistry, serves as a sharp tool in the battle against porphyrias. Its impact reminds us to keep pushing science forward while standing alongside those who need support right now.
| Names | |
| Preferred IUPAC name | iron; (3S,8S,13S,18S)-3,8,13,18-tetraethyl-2,7,12,17-tetramethyl-23,24-dihydroporphyrin-2,7,12,17-tetraylium-5,10,15,20-tetrayl tetrapropanoate chloride |
| Other names |
Ferriheme Hemin chloride Ferriprotoporphyrin IX chloride Panhematin |
| Pronunciation | /ˈhiːmɪn/ |
| Preferred IUPAC name | iron(III);(3S,8S,13S,17S)-13-ethyl-3,8,17-tris(2-hydroxyethyl)-2,7,12,17-tetramethyl-21,23,24,25-tetraaza-1,6,11,16-tetrapyrrolen-21-ylium-24,25-diide; (2E)-2-hydroxyprop-2-enoic acid |
| Other names |
Ferriheme Heminic chloride Protohemin Hemin chloride Ferriprotoporphyrin IX chloride |
| Pronunciation | /ˈhiːmɪn/ |
| Identifiers | |
| CAS Number | 16009-13-5 |
| Beilstein Reference | 1898315 |
| ChEBI | CHEBI:35144 |
| ChEMBL | CHEMBL1204 |
| ChemSpider | 54675 |
| DrugBank | DB01011 |
| ECHA InfoCard | ECHA InfoCard 100.027.467 |
| EC Number | EC 4.2.1.1 |
| Gmelin Reference | 78738 |
| KEGG | C00032 |
| MeSH | D006462 |
| PubChem CID | 26945 |
| RTECS number | GL7890000 |
| UNII | 31D4GT1JF0 |
| UN number | UN2811 |
| CompTox Dashboard (EPA) | DTXSID8020823 |
| CAS Number | 16009-13-5 |
| 3D model (JSmol) | `3D model (JSmol) string of Hemin: "data/hem.cml"` |
| Beilstein Reference | 1208731 |
| ChEBI | CHEBI:35132 |
| ChEMBL | CHEMBL1204 |
| ChemSpider | 53490 |
| DrugBank | DB01007 |
| ECHA InfoCard | 100.029.183 |
| EC Number | EC 235-131-9 |
| Gmelin Reference | 81478 |
| KEGG | C00032 |
| MeSH | D006461 |
| PubChem CID | 24894258 |
| RTECS number | GF9860000 |
| UNII | 4B40J45L23 |
| UN number | UN2811 |
| CompTox Dashboard (EPA) | DTXSID7046148 |
| Properties | |
| Chemical formula | C34H32ClFeN4O4 |
| Molar mass | 652.0 g/mol |
| Appearance | Dark reddish-brown to black crystalline powder |
| Odor | odorless |
| Density | 1.35 g/cm³ |
| Solubility in water | 0.0016 g/L (25 °C) |
| log P | -4.2 |
| Vapor pressure | <0.0000001 mmHg (25 °C) |
| Acidity (pKa) | Acidity (pKa): 4.05 |
| Basicity (pKb) | 8.12 |
| Magnetic susceptibility (χ) | +2250e-6 cm³/mol |
| Refractive index (nD) | 1.444 |
| Viscosity | 20~30 mPa.s |
| Dipole moment | 3.48 D |
| Chemical formula | C34H32ClFeN4O4 |
| Molar mass | 652.94 g/mol |
| Appearance | dark reddish-brown to black crystalline powder |
| Odor | odourless |
| Density | 1.35 g/cm³ |
| Solubility in water | Insoluble |
| log P | -2.9 |
| Vapor pressure | Vapor pressure: Negligible |
| Acidity (pKa) | 12.5 |
| Basicity (pKb) | 13.52 |
| Magnetic susceptibility (χ) | -282.0e-6 cm³/mol |
| Refractive index (nD) | 1.435 |
| Viscosity | 15~25 mPa.s |
| Dipole moment | 3.58 D |
| Thermochemistry | |
| Std molar entropy (S⦵298) | 246.0 J/mol·K |
| Std enthalpy of formation (ΔfH⦵298) | -1537.1 kJ/mol |
| Std molar entropy (S⦵298) | 253.6 J·mol⁻¹·K⁻¹ |
| Std enthalpy of formation (ΔfH⦵298) | -243.1 kJ/mol |
| Pharmacology | |
| ATC code | B06BA03 |
| ATC code | B06AB03 |
| Hazards | |
| GHS labelling | GHS02, GHS07 |
| Pictograms | GHS07,GHS08 |
| Signal word | Warning |
| Hazard statements | H302 + H332: Harmful if swallowed or if inhaled. |
| Precautionary statements | P264, P270, P301+P312, P330, P501 |
| Flash point | > 220 °C |
| Autoignition temperature | > 360 °C |
| Lethal dose or concentration | LD50 intravenous mouse 64 mg/kg |
| LD50 (median dose) | LD50 (median dose): Mouse intravenous 46 mg/kg |
| NIOSH | NOT LISTED |
| PEL (Permissible) | Not established |
| REL (Recommended) | 50-100 mg daily |
| Main hazards | Causes eye, skin, and respiratory irritation; harmful if swallowed. |
| GHS labelling | GHS02, GHS07 |
| Pictograms | GHS06, GHS08 |
| Signal word | Warning |
| Hazard statements | H315, H319, H335 |
| Precautionary statements | P261, P280, P304+P340, P312, P405, P501 |
| NFPA 704 (fire diamond) | 2-1-0 |
| Flash point | > 230 °C |
| Autoignition temperature | 215 °C |
| Lethal dose or concentration | LD₅₀ (intraperitoneal, mouse): 120 mg/kg |
| LD50 (median dose) | LD50 (median dose): >5 g/kg (rat, oral) |
| NIOSH | 8000 |
| PEL (Permissible) | 5 mg/m3 |
| REL (Recommended) | 150 mg daily |
| Related compounds | |
| Related compounds |
Chlorins Porphyrins Protoporphyrin IX Hematin |
| Related compounds |
Protoporphyrin IX Heme Hematin |