P-Nitrobenzoyl Chloride (PNBC): More Than a Chemical Name

Historical Development

P-Nitrobenzoyl chloride traces its roots to foundational shifts in organic synthesis that defined late nineteenth and early twentieth-century chemistry. Researchers craved new ways to introduce functional groups onto aromatic rings, and the nitro group promised wild new reactivity. Early reports from German chemists discuss p-nitrobenzoic acid as a stepping stone and documented the transformation of acids to corresponding acid chlorides using reagents like thionyl chloride and phosphorus pentachloride. This path ushered in the reliable lab access chemists enjoy today. Friends in lab coats learned to respect PNBC’s assertive scent and reactive nature, realizing safe handling made or broke a researcher's day. Not just a reagent, PNBC embodies the ingenuity and persistence of generations who harnessed its power while keeping safety and purity under tight control.

Product Overview

PNBC, or para-nitrobenzoyl chloride, keeps plenty of molecular drama up its sleeve. Its formula, C7H4ClNO3, points to a benzene ring stacked with a nitro group and an acyl chloride. This unique arrangement turns an otherwise unassuming powder into an essential tool for synthetic, pharmaceutical, and research labs. Chemists value its role in crafting dyes, pharmaceuticals, and more, where its knack for transferring benzoyl groups brings operational efficiency no other chemical quite matches. The molecule’s structure sets the foundation for wide-ranging chemical adventures, whether it’s delivering custom-tailored building blocks or helping map out tough-to-characterize protein structures.

Physical & Chemical Properties

This pale yellow, crystalline substance doesn’t blend in with sweetness and light. PNBC exhibits a high melting point near 78–80°C and releases a pungent, almost eye-watering odor familiar to seasoned chemists. It demonstrates low solubility in water, enabling selective reactions when suspended or dissolved in organic solvents—like ether or chloroform. That makes creative reaction setups a reality; I’ve seen researchers choose solvents specifically to corral PNBC’s reactivity and harness its unique behavior in multi-step syntheses. The nitro group at the para position amps up the molecule’s electron-withdrawing power, making the acyl chloride briskly reactive even at lower temperatures. Its density sits near 1.46 g/cm3, and it resists easy vaporization—though not enough to waive good fume hood etiquette.

Technical Specifications & Labeling

Manufacturers bottle up PNBC with clear labeling: minimum assay, water content, melting point, and purity percentages always show up. Maximum allowable impurities such as unreacted p-nitrobenzoic acid, moisture, and other halogenated byproducts get special attention, with chromatograms and molecular fingerprint data available from reliable suppliers. I’ve never taken shortcuts here—errors in labeling and incorrect technical sheets not only derail projects but put users at direct risk. Industry standards highlight the need for amber glass containers to keep light-sensitive material stable over weeks or even months. It pays to verify packaging for leak-proof seals, warning labels for corrosivity and toxicity, and what to do in a spill—any lapse in labeling transparency deserves scrutiny from lab managers.

Preparation Method

The routine approach begins with p-nitrobenzoic acid—a common asset in many labs. By applying thionyl chloride or phosphorus pentachloride, chemists trigger the release of hydrogen chloride gas and capture PNBC in the organic layer. My time running these preparations underscored the importance of temperature control; the reaction heats up quickly, so keeping a steady hand on the ice bath and slow reagent addition helps control the exotherm. Filtration, distillation, and careful removal of volatile byproducts round out the method. Having run these in both small and semi-industrial settings, minor lapses in water exclusion lead to hydrolysis and wasted yield. Each batch ends with rigorous assay and crystallinity checks—clear evidence how hands-on care boost both yield and purity.

Chemical Reactions & Modifications

PNBC’s biggest utility shines in acylation reactions, where it reacts swiftly with alcohols and amines to generate esters and amides. Pharmaceutical teams count on these steps to build molecular frameworks flexibly and on demand. Its eager reactivity with nucleophiles sometimes calls for a mediator base like pyridine, neutralizing acidic byproducts and smoothing the path to clean product formation. PNBC helps chemists tack on p-nitrobenzoyl “tags” for protein sequencing, offering a structural “marker” that signals modified residues in peptide analysis. It also feeds larger syntheses for dyes, stabilizers, and specialty polymers. The molecule’s reactivity isn’t purely a blessing—it can lead to side reactions or over-acylation if not carefully monitored, reminding every synthetic chemist that skill and studied patience always win the day.

Synonyms & Product Names

Over the years, those in chemical supply chain circles have heard p-nitrobenzoyl chloride called everything from PNBC to 4-nitrobenzoyl chloride and para-nitrobenzoyl chloride. European publications sometimes abbreviate differently, but the industry has settled on PNBC for clarity. Chemical catalogues list alternative spellings to help prevent dangerous mix-ups. The CAS registry number, 122-04-3, carves out a permanent identity in commerce and scientific literature.

Safety & Operational Standards

Direct contact with PNBC brings health risks. Its corrosive nature targets skin, mucous membranes, and lungs. I recall my first live demo, where an errant drop on a glove prompted an instant switch to new protective gear. Proper PPE, fume hood work, and full emergency kits aren’t negotiable here—no cutting corners. PNBC reacts with water and alcohol, pumping out hydrogen chloride gas that stings the eyes and burns the skin. Industrial players design storerooms with strict humidity control and acid-neutralizing chemicals nearby. The Occupational Safety and Health Administration (OSHA) and equivalent European agencies post strict guidelines for safe storage, handling, and disposal. Any spill means quick, informed response using soda ash or lime and full ventilation. Old-timers will joke about the risks but never shirk from scrupulous adherence to standards.

Application Area

PNBC finds a home across scientific fields. Pharmaceutical teams synthesize active molecules, using the nitrobenzoyl group as a “mask” in stepwise buildouts of antibiotic and anticancer products. Dye chemists use PNBC to build vibrant azo pigments and colorants, trading on the special reactivity of the nitro and acyl groups. Polymers and plastics manufacturers design monomers and curing agents around this molecule, exploiting its reactivity for tailored end-use properties. Research labs find fresh value in attaching the nitrobenzoyl group to amino acid residues, sequencing proteins and mapping enzyme function by the unique signatures of the tag. The scent and handling challenges don’t deter anyone who sees just how much flexibility PNBC offers for ambitious synthetic goals.

Research & Development

Lab-based R&D groups focus hard on pushing PNBC’s frontiers: crafting new analogs, exploring regioselective acylation, and controlling energy usage and waste output. One area gaining traction focuses on green synthesis—industrial teams push to replace classic reagents like thionyl chloride with milder, safer alternatives. I’ve seen solvent system research help reduce hydrolysis, cut down on purification steps, and increase yield, answering the call for reduced cost and waste. Collaborators from both the pharmaceutical and fine chemistry worlds track down improved protocols for purification, less hazardous waste, and new catalytic systems. These efforts aim to keep PNBC relevant, competitive, and safe while tightening regulatory compliance.

Toxicity Research

The nitro group raised eyebrows for years due to its reactivity and potential to form mutagenic intermediates. Toxicity studies on PNBC document skin, eye, and respiratory tract hazards using both rodent and cell-culture models. Acute exposure highlights corrosive injury and inflammatory responses. Long-term data builds a more complex picture: animal tests demonstrate that chronic inhalation can drive tissue changes or exacerbate asthma-like symptoms. Environmental review articles document the potential of PNBC to harm aquatic life, especially when improperly disposed. Responsible manufacturers and users press for full adherence to safety protocols, investing in exhaust filtration, spill prevention, and toxicological screening. Here’s where oversight meets everyday practice: regular safety drills, clear labeling, and sustained investment in engineering controls cut workplace injuries and accidental releases.

Future Prospects

PNBC’s outlook stretches beyond today’s standard applications. Researchers eye the molecule as a launch point for green acylation techniques, asking how to trim risk while protecting product quality. Ongoing innovations in automation and continuous-flow chemistry unlock faster, safer, and more reliable processes for PNBC and its cousins. Start-ups and academic groups tinker with enzyme-based modifications, seeking to reduce environmental burden and dodge harsh reagents. The growing influence of green chemistry principles keeps pushing PNBC synthesis and application to cleaner, smarter, and more responsible horizons. With demand strong across sectors, the molecule stands set for a future where transparency, control, and sustainability define every new use.



What is the chemical formula and molecular weight of P-Nitrobenzoyl chloride (PNBC)?

What’s P-Nitrobenzoyl Chloride, Anyway?

P-Nitrobenzoyl chloride, often called PNBC among chemists, comes up in labs and factories all over the world. I first ran into it in a college synthesis class, hands shaking, goggles pressed to my face, trying to measure exactly the right amount. Its chemical formula is C7H4ClNO3, and it has a molecular weight of 185.57 grams per mole. That’s about the size you expect from a benzoic acid derivative with a nitro group and a chloride tacked on for reactivity.

Why the Details Matter

Getting the formula and molecular weight right isn’t just trivia for a pop quiz. If you work in organic synthesis, a mistake here means hours lost and budgets busted. PNBC is used to bring a benzoyl group onto molecules, especially in pharmaceutical or dye intermediate synthesis. A miscalculation in molecular weight throws off the reactant ratios, which can mean incomplete reactions or nasty byproducts.

I remember an early boss hammering into us the importance of double-checking weights and formulas. Look up a chemical with the wrong formula, and you might order a powder that doesn’t just ruin your experiment but could react the wrong way with your equipment, or worse, endanger someone’s health.

Real Dangers and Real Rewards

PNBC’s no joke when it comes to safety. The compound can easily irritate the eyes, skin, and lungs. The nitro group makes the molecule more reactive and hazardous if handled carelessly. Industrial accident reports keep showing injuries linked to improper storage or quick-and-dirty handling. Gloves, fume hoods, and vented storage aren’t optional in a lab or factory using this stuff. A few minutes without protection and PNBC will remind you it’s not just another bottle on the shelf.

But on the flip side, it’s a workhorse. Chemists lean on PNBC when building a new drug scaffold or creating custom dyes for electronics. The chloride bond snaps off with the right reagents, letting you bolt the benzoyl group onto pretty much any organic backbone. The nitro group’s electron-withdrawing nature makes the whole process more predictable. That’s reliability you can count on when a multimillion-dollar batch of material hangs in the balance.

Getting Procurement and Sourcing Right

Reliable sources matter. Fake chemicals or mislabeled products sometimes flood the market, especially with cost pressures. Labs and plants getting their PNBC need to check supplier credentials and chemical test results. I’ve seen researchers stuck with useless or dangerous material because the sample turned out impure—extra acid or missing nitro group. That’s not a small hiccup. Pharmacists and chemists should work only with well-vetted, certified suppliers and always verify what comes in through independent checks. This does more than save money; it protects the whole project and the people handling the chemical.

Aim for Better Practices

As the chemical industry shifts, more companies look toward greener alternatives and safer practices. PNBC’s hazards make it a candidate for improvement, whether through better protective systems or exploring less aggressive reagents where possible. Ongoing research into process efficiency, waste reduction, and alternative synthesis routes benefits both workers and the environment. Those changes help companies keep up with rising expectations for health and sustainability, which shape not just profits but long-term trust with end users and regulators.

What are the main applications and uses of P-Nitrobenzoyl chloride?

What Stands Out in Research and Industry

P-Nitrobenzoyl chloride hasn’t crossed paths with most people outside a lab, but its story rolls quietly through many corners of chemistry. It’s a highly reactive compound, known for a sharp odor and ability to spark transformation in other molecules. If you’ve watched graduate students bustle in a synthetic organic chemistry lab, you’ve probably caught a whiff of it lingering in reagent cupboards. It shows up because it’s genuinely useful—not just a curiosity sitting in a bottle.

Core Role in Pharmaceutical Development

Labs working to build new drugs turn to p-nitrobenzoyl chloride for its knack in forming intermediate compounds. Medicinal chemists often need to attach the p-nitrobenzoyl group onto amines or alcohols. This helps them mask, or “protect,” a particular part of a molecule during tricky reactions. I remember projects where our team struggled with sensitive amines, and this chemical cut through roadblocks. It played a part in shaping building blocks for anti-cancer agents, antibiotics, and painkillers. After the dust settled in the synthesis, it was easy to peel the protective group off. These kinds of protective strategies help companies cut development time and avoid wasteful detours.

Diagnostics and Peptide Chemistry

Diagnostic and biotech groups also use p-nitrobenzoyl chloride to tag biological molecules, especially amino acids and small peptides. During amino acid sequencing, attaching the p-nitrobenzoyl group makes certain molecules easier to spot downstream, whether on a chromatogram or through spectroscopy. Spotting one bright yellow peak can mean the difference between a clear result and a messy one. This has carried over into automated peptide synthesizers, where precision really counts. For researchers chasing disease-signature proteins or allergens, these little details spell the difference between trusted results and wasted weeks.

Industrial Dyes and Material Science

Move past the pharmacy shelf, and p-nitrobenzoyl chloride steps into the world of industrial dyes and polymers. The chemical’s role as an acylating agent lets it tweak the colors, durability, or solubility of synthetic dyes. Companies want their fabrics to keep their greens and blues after endless cycles in washing machines. I’ve watched dye chemists blend small amounts of this reagent into their recipes, knowing it can bump up a product’s resistance to fading or bleeding. Even outside the textile world, polymer specialists use it for engineering specialty plastics or coatings that defend against heat or chemicals.

Safety Concerns and Responsible Handling

Anyone handling p-nitrobenzoyl chloride knows how quickly the compound can react, especially with water. Its fumes attack the nose and eyes, and it can burn skin instantly. Labs spend extra time on training because even a single accident with this stuff can put a project on hold. Production lines and academic departments need steady protocols—think chemical hoods, gloves, and rescue showers—not just for compliance, but for real peace of mind. Some manufacturers push for closed systems or swap in milder alternatives where possible, but for certain syntheses, nothing else achieves the same precision. A future with stronger focus on safety, worker education, and green chemistry could protect both people and progress in this field.

What are the proper storage conditions and shelf life for PNBC?

Why Storage Matters for PNBC

People working with chemicals like PNBC know that mishandling can turn an asset into a hazard. PNBC, short for para-nitrobenzyl chloride, sees use in a range of processes, from lab work to industrial manufacturing. Poor storage might not just spoil the product—it can bring financial loss, lower output quality, and even place health at risk. My lab days taught me: skipping a few steps in storing a chemical can turn the simplest experiment into a headache.

Recommended Storage Conditions

Proper storage starts with a cool, dry place away from anything that can spark a fire. PNBC should not sit near windows or direct sunlight because heat speeds up chemical breakdown. Direct heat makes the compound unstable, and you don’t want to open a container just to find degraded or altered material.

A consistent temperature between 2°C to 8°C works best. Everyday lab refrigerators usually keep within this range. At home, think about why you don’t store all food at room temperature—same applies here. Temperature swings (one day cold, next day warm) allow condensation to form inside, which might start unwanted reactions. I recall a time a batch spoiled because staff ignored this basic rule; months of planning went straight in the trash.

Humidity creeps up as another culprit. When PNBC meets water vapor, it can break down or react in unpredictable ways. Keep the cap shut tight and use containers built to lock out air and moisture. Some teams go a step further by dropping in desiccant packs. The idea is simple: moisture damages value.

Avoiding Common Storage Hazards

Many forget about labeling or mix up similar-looking chemicals. Reusing old containers, skipping expiration checks, or crowding the shelf builds trouble. I once watched a colleague dust off a bottle, read a smudged label, and nearly grabbed the wrong reagent—an easy way to invite mistakes or cross-contamination. Good records on purchase date and storage log keep confusion away.

There’s also the risk of storing PNBC near acids, bases, or oxidizing agents. These materials can react dangerously, leading to fumes, fires, or even explosions. So, keep incompatible chemicals on separate shelves, apart from PNBC. I saw a near miss in an industrial plant from this exact oversight—a reminder that organization beats luck every time.

How Long Does PNBC Last?

Most chemical suppliers set shelf life for PNBC at about two years under recommended storage. This count starts from the bottling date, so opening the container won’t reset the clock. Regular checks help spot crystals, clumping, or color changes. These signs often mean trouble brewing inside the bottle. In my own experience, old or clumpy material ruined an entire synthetic batch, costing both money and weeks of work.

Expired PNBC doesn’t just weaken results; it brings the risk of toxic byproducts or unreliable outcomes. Outdated stock demands safe disposal—never send it straight down the drain. Strict disposal routines do more than keep rules—protecting coworkers and the environment.

Building a Safer, More Reliable Lab

There’s more to good storage than following a checklist. Training staff on chemical handling, updating safety protocols, and running regular stock audits keep labs safe. Simple tools like clear labels and inventory logs make a difference. My habit: set calendar reminders for quality checks, track dates, and stay consistent with discipline. Practicing good storage and timely disposal ensures every chemical in the cabinet remains safe and effective.

Getting storage right with PNBC builds trust between product, user, and business. Quality always starts with care at every step—from the moment the bottle arrives until it leaves the lab.

What are the safety precautions and hazards associated with PNBC handling?

Why PNBC Handling Matters for Safety

PNBC stands out as a chemical that demands respect from anyone working with it. My years in manufacturing environments taught me that overconfidence around hazardous chemicals often invites disaster. PNBC’s reactions can be swift and unforgiving: its fumes, dust, and accidental spills have sent plenty of people to the emergency room. Too many folks underestimated the risks, thinking gloves and a mask would cover every base. That’s not the case here. Relying on shortcuts or ignoring protocols with PNBC handling risks injury, long-term health problems, and unintended environmental impact.

Understanding the Main Hazards

Ask anyone who’s handled PNBC, and you’ll hear about the pungent smell and irritation it causes. The skin doesn’t forget a splash. PNBC’s dust and vapors irritate the eyes, respiratory system, and can trigger allergic reactions even in low doses. Once, a coworker forgot his safety goggles and rinsed his eyes for almost an hour. Even after following the recommended rinsing protocol, he struggled with eye pain for days.

Long-term exposure brings up another concern. Studies from workplaces using PNBC consistently link unprotected, chronic contact to problems such as dermatitis, asthma, or even liver issues. Ignoring ventilation or skipping respirators causes inhalation of dust or vapor that the lungs can’t shrug off.

Precautions That Protect Real People

My approach involves real steps anyone can take seriously. Always suit up with splash-proof goggles, gloves resistant to solvents, and full-coverage clothing. A good fit makes a difference—loose sleeves don’t protect wrists, and half-hearted eye gear won’t keep out a sudden splash.

Work areas using PNBC should go heavy on ventilation. I’ve seen shops install local exhaust systems right above benches and fume hoods that run constantly while PNBC gets handled. These setups cut airborne concentrations and prevent buildup.

Training and refreshers deserve more attention than they usually receive. Sitting through hands-on hazard communication training can feel repetitive, but I remember people catching mistakes during these sessions that would’ve caused trouble. Regular drills and scenario discussions keep everyone sharp, not just new hires.

Storage and Emergency Planning

Locking up PNBC in tightly sealed containers and labeling them clearly avoids accidental mix-ups. I store these containers far from heat sources or anything reactive. Checking compatibility charts seems like a chore, but it spares everyone messy surprises. If a spill does happen, spill kits with absorbent pads and neutralizing agents need to sit right where the chemical gets used.

One time an emergency shower saved a guy’s skin. He moved without thinking, but the team kept the shower and eyewash stations within a few steps of every workstation. Every second counts. That combination of good design and practice makes a stressful emergency much less dangerous.

Solutions for a Safer Workplace

Looking at the bigger picture, leadership that sets high standards for chemical safety makes the biggest difference. Investing in ventilation upgrades, setting up airflow checks, or keeping PPE in good shape pays off in fewer accidents. Transparent policies, clear signage, and strong accountability prevent “shortcut culture” from creeping in. Nobody should have to learn about PNBC hazards through trial and error. Real commitment and practical precautions protect lives and keep work moving forward.

What is the standard packaging size and availability for P-Nitrobenzoyl chloride?

Understanding Typical Packaging Choices

In most labs and manufacturing sites I’ve come across, P-Nitrobenzoyl chloride lands on the shelf in sturdy containers designed for both safety and efficiency. The most common sizes I see range between small amber glass bottles of about 25 grams to bulkier metal or HDPE drums that can carry up to 25 kilograms. Smaller bottles work for research or analytical work, where you only need a pinch to run a few tests. Once a project ramps up or a plant moves into scale-up, those busy labs order much larger drums—sometimes even in fiberboard cartons with double polyethylene liners, just to keep moisture out and cut down on contamination.

Companies in the chemicals market rarely settle for fancy packaging unless there’s a safety or stability benefit. Here, P-Nitrobenzoyl chloride earns its tough packaging because it reacts easily with water in the air, putting lab staff and stock at risk if someone forgets to close a lid. You’ll often find extra tape over jar lids or security seals intact. From my experience, if the room smells even a bit harsh when you open a new drum, the container design did its job: keeping the product protected on its journey.

Who Sells It, and in What Quantities?

Most global chemical suppliers keep P-Nitrobenzoyl chloride in their catalog year-round. I’ve noticed the leading scientific supply houses offer it online, sometimes with next-day shipping. Research labs usually stick with 5, 25, or 100 gram options, but some academic institutions or pilot plants buy in half-kilo or one kilo lots to keep workflow smooth. Scale-up users or pharmaceutical companies can get as much as 25 kilograms at once—usually after passing a few compliance hoops because of handling rules.

For buyers in countries with strict import controls, local distributors or resellers provide smaller packs: their shelves often hold 100 gram plastic jars with tamper-evident closures, and sometimes re-bottle the chemical in batches suited to frequent turnover. I’ve worked with labs where, to minimize waste and exposure, one team buys the drums and divides them up into brown glass vials so no one’s tempted to keep a large drum open for too long.

Why Size Matters for Safety and Cost

Choosing the right container size isn’t just about convenience. P-Nitrobenzoyl chloride degrades fast if moisture sneaks in, wrecking purity and causing headaches in synthesis steps. From my own research days, storing large quantities without proper airtight seals led to unusable batches—triggering both expensive waste disposal and delays. On top of that, smaller packaging means fewer spills when measuring out doses, reducing chances of skin burns or accidental inhalation.

Cost also comes into play. Bulk buying usually trims the price per gram, but labs need good inventory systems or they risk writing off overexposed allotments. For organizations with slower usage, it’s smarter to spend a bit extra on small packs and keep the rest safely stored in a chemical storehouse.

Strategies for Sustainable and Compliant Sourcing

Smart procurement rests on finding the packaging size that matches your actual consumption and local storage laws. If I’ve learned anything, it’s to check supplier reviews for shipment quality and ask about their packaging methods. Buyers aiming for green chemistry also look out for recyclable packaging and vendors committed to safe, sealed transit. Up-to-date safety data sheets and clear hazard labeling ensure not just compliance, but peace of mind for everyone handling the material—be it in academia, biotech startups, or the chemical industry’s giant plants.

P-Nitrobenzoyl chloride PNBC
Names
Preferred IUPAC name 4-nitrobenzoyl chloride
Other names 4-Nitrobenzoyl chloride
p-Nitrobenzoyl chloride
Para-Nitrobenzoyl chloride
Pronunciation /ˈpiː ˈnaɪ.trəʊ.bɛnˌzɔɪl ˈklɔː.raɪd/
Identifiers
CAS Number 122-04-3
3D model (JSmol) `JSmol` 3D model **string** for **P-Nitrobenzoyl chloride (PNBC)**: ``` CC1=CC=C(C=C1C(=O)Cl)[N+](=O)[O-] ``` This is the **SMILES string** suitable for JSmol and other molecular viewers.
Beilstein Reference 331876
ChEBI CHEBI:51512
ChEMBL CHEMBL139707
ChemSpider 167791
DrugBank DB14015
ECHA InfoCard 03d3b73a-847e-43e5-a4b7-099059a51ed3
EC Number 202-714-7
Gmelin Reference 6082
KEGG C14326
MeSH D010787
PubChem CID 7094
RTECS number CU5950000
UNII F9T46386R1
UN number UN1664
CompTox Dashboard (EPA) DTXSID0024685
Properties
Chemical formula C7H4ClNO3
Molar mass 169.55 g/mol
Appearance White to pale yellow crystalline powder
Odor Pungent
Density 1.53 g/cm³
Solubility in water Reacts with water
log P 1.91
Vapor pressure 0.02 hPa (20 °C)
Acidity (pKa) 1.0
Basicity (pKb) 11.08
Magnetic susceptibility (χ) -38.6·10⁻⁶ cm³/mol
Refractive index (nD) 1.6090
Viscosity Viscosity: 1.576 mPa.s (20°C)
Dipole moment 3.13 D
Thermochemistry
Std molar entropy (S⦵298) 309.7 J·mol⁻¹·K⁻¹
Std enthalpy of formation (ΔfH⦵298) -252.7 kJ/mol
Std enthalpy of combustion (ΔcH⦵298) -653.5 kJ·mol⁻¹
Pharmacology
ATC code R01AX
Hazards
GHS labelling GHS02, GHS05, GHS06, GHS07
Pictograms GHS05,GHS06,GHS08
Signal word Danger
Hazard statements H302, H314, H317, H319, H331, H335
Precautionary statements Precautionary statements: P261, P280, P305+P351+P338, P337+P313, P405, P501
NFPA 704 (fire diamond) 3-3-2-OX
Flash point 80°C
Autoignition temperature Unknown
Lethal dose or concentration LD50 oral rat 1000 mg/kg
LD50 (median dose) LD50 (median dose): Oral rat LD50: 640 mg/kg
NIOSH SN 1225000
PEL (Permissible) PEL (Permissible Exposure Limit) for P-Nitrobenzoyl chloride (PNBC) is not specifically established by OSHA.
REL (Recommended) 0.1 mg/m3
IDLH (Immediate danger) IDLH: 5 mg/m3
Related compounds
Related compounds Benzoyl chloride
m-Nitrobenzoyl chloride
p-Nitrobenzoic acid
p-Nitroaniline
p-Nitrobenzaldehyde