1-Bromo-3-Chloropropane: A Practical Perspective

Historical Development

Chemists learned to prepare halogenated hydrocarbons long before many of us started thinking about organic chemistry. 1-Bromo-3-chloropropane falls into the category of these early discoveries, sliding its way into lab manuals by the middle of the 20th century. These compounds popped up frequently in synthetic routes, especially during the rush to understand substitution mechanisms and the behavior of multiple halogen atoms on a simple alkane backbone. Around this time, industrial chemists were looking for manageable intermediates for more complex products—the sort that keep factories humming. The adoption of 1-Bromo-3-chloropropane gained speed as researchers realized that it could serve as a reliable building block, somewhere between commodity chemical and targeted reagent. By the 1970s, catalogs featured the compound as a go-to for exploring the chemistry of alkyl halides and their role in everything from pharmaceuticals to materials research.

Product Overview

1-Bromo-3-chloropropane sits among those halogenated propanes that offer enough reactivity for organic synthesis yet show enough stability to handle, store, and ship across borders. The structure includes a three-carbon chain—one end capped with bromine, the other with chlorine. This specific arrangement sets it apart from its cousins like 1,3-dibromopropane or 1-chloropropane. Its unique electron distribution grants it roles in nucleophilic substitution reactions, which has kept it in steady demand for researchers who need a dual-activated propyl group. Among the many chemicals with similar uses, this one stands out thanks to its dual halogen pattern, which offers some unconventional reactivity compared to single-halide analogs.

Physical & Chemical Properties

1-Bromo-3-chloropropane has a clear, colorless, oily liquid form when sitting at room temperature. The molecular formula, C3H6BrCl, weighs in with a molar mass of about 157.44 g/mol. Its boiling point stays close to 142°C, and its melting point usually lands around -60°C. The density hovers around 1.6 g/cm³, so it settles at the bottom if mixed with water—which isn’t much of a risk because it barely dissolves. In terms of polarity, the molecule invites nucleophilic attack, as bromine’s electron-withdrawing punch sits opposite to the slightly less electronegative chlorine. The pairings on the three-carbon skeleton give the molecule a slightly higher dipole moment, which gets attention in chemical transformations. This chemical won’t ignite unless heated above 100°C, but proper ventilation helps avoid buildup of vapors that can irritate the nose and throat.

Technical Specifications & Labeling

Manufacturers bottle 1-Bromo-3-chloropropane under various grades, aiming for 98% or higher purity for research labs, and a slightly less stringent grade for industrial usage. Labels require the UN number (2708), proper hazard pictograms for corrosivity and inhalation risk, and clear mention of its halogen content. Good technical sheets list boiling point, density, purity, and recommended storage conditions—typically cool, dry, well-ventilated spaces with secure, chemical-resistant bottle seals. Labels follow both GHS and regional rules for shipping, especially for companies working across countries. Shipment often requires documentation on toxicity and flammability, as carriers ask pointed questions about halogenated solvents.

Preparation Method

Production usually involves a free-radical halogenation sequence, using 1,3-dichloropropane or 1,3-dibromopropane as starting points. Chemists often treat 1,3-dichloropropane with sodium bromide and a phase transfer catalyst, bumping chloride with bromide via a classic Finkelstein reaction. The process depends heavily on temperature control, as too much heat leads to overbromination and unwanted byproducts, wasting both reagents and time. Washing, drying, and fractional distillation finish the preparation, isolating the product from excess salts, unreacted starting material, and side-products. Every step demands attention to personal protection and fume control, as escaping vapors can quickly cause headaches—or worse—if left unchecked. Industrial facilities rely on closed systems to prevent operator exposure and limit environmental emissions.

Chemical Reactions & Modifications

1-Bromo-3-chloropropane finds regular use in organic synthetic labs, catalyzing discussions around the SN2 mechanism. Both halogen ends activate the molecule for various substitutions—a nucleophile can swap out the bromine or the chlorine with relative ease. Students often start by reacting it with sodium azide to make azido derivatives, which are then reduced into amines for use in pharmaceutical intermediates. Alkoxide ions convert it into ethers, and common thiols make thioether linkages. Grignard and organolithium reagents interact with the bromine, providing an entry point for carbon–carbon bond formation. Its ability to carry two different leaving groups means one can perform stepwise reactions; swap chlorine for a new nucleophile, then repeat at the bromine end. These features drive custom synthesis in drug discovery and advanced materials engineering, where tailored molecular skeletons matter.

Synonyms & Product Names

Chemists know this compound under several names, with 1-bromo-3-chloropropane the formal IUPAC designation. Catalogs sometimes call it 3-chloropropyl bromide, or add prefixes like α-chloro-γ-bromopropane. CAS numbers offer another search anchor: 109-70-6. In some circles, the shorthand BCP or BC-propane appears, especially in process notes or bulk ordering. These names pop up in online databases, so researchers scan for them all when reviewing data or ordering supplies. R&D teams learn these variants—as a single misread in inventory sheets means delays or miscalculations.

Safety & Operational Standards

Handling 1-Bromo-3-chloropropane calls for careful safety measures. Vapors irritate the respiratory tract, so chemical fume hoods become standard equipment any time bottles leave the stockroom. The liquid stings skin and eyes, with enough evidence pointing to sensitizing effects after repeated exposure. Nitrile gloves, splash goggles, and long sleeves provide real-world protection, and written protocols include rapid decontamination steps for accidental spills. Storage requires away-from-flame placement, using chemical-resistant, labeled bottles. Clean, organized shelves and routine inspections reduce accident risk, as bottles degrade over time. Disposal routes take the halogen content into account: municipal drains get ruled out, and licensed hazardous waste contractors haul away the spent material. Regular safety audits and emergency drills ensure that a single cracked bottle doesn’t spiral out of control in an educational or industrial setting.

Application Area

1-Bromo-3-chloropropane attracts most attention in organic synthesis, where it acts as a versatile intermediate for building more complicated molecules. Pharmaceutical research benefits from its dual reactivity—new drug scaffolds often rely on introducing or modifying functional groups at both ends of a molecule, which this compound facilitates. Specialty polymer manufacturers sometimes use it to link monomers in chain-transfer reactions, taking advantage of both halogens’ leaving group abilities. Certain agrochemical discoveries lean on halogenated intermediates for tweaking bioactivity, solubility, or persistence in the field. Material scientists looking for new coatings or adhesives sometimes trial the compound as a linker between functional surfaces, especially for applications that need robust connections in hostile environments. Its role as a solvent is rare, but appears in density gradient centrifugation, where its unique physical properties help separate biological molecules without deactivating them.

Research & Development

Laboratories across research universities and the private sector keep 1-Bromo-3-chloropropane on hand. Its dual halogen pattern sparks plenty of curiosity about site-selective substitution. Graduate students synthesize derivatives to probe molecular mechanism or help model enzyme-substrate interactions. Combinatorial chemistry teams exploit its use in building small libraries of analogs for biological screening. Companies seeking new process routes for fine chemicals sometimes start with this molecule, running trials to determine if it gives better yields or cleaner products than other halogenated propanes. Patents referencing this compound show up in areas like antiviral agents, ambulance of new crosslinkers in high-performance polymers, and exploratory catalysts. As interest grows in green chemistry, some labs run lifecycle analyses to compare its environmental load against simpler or more readily available alkyl halides.

Toxicity Research

Long-term studies on halogenated propanes highlight several safety themes for 1-Bromo-3-chloropropane. Researchers measuring acute toxicity in rodents found moderate toxicity by inhalation or ingestion, triggering symptoms like labored breathing or sluggishness at elevated doses. Data indicate repeated exposure leads to liver and kidney stress, and the compound displays a moderate tendency to bioaccumulate in fatty tissue. Eye or skin exposure causes inflammation, with periodic findings of dermatitis after accidental splashes. In vitro tests show mutagenic activity at high doses, which puts pressure on industry and academia to reinforce personal protection and limit waste discharge. Regulatory agencies in the United States and Europe classify the chemical as hazardous, with recommended exposure limits in lab settings. Routine air sampling and medical monitoring for frequent handlers play a role in occupational safety, especially for groups at the front lines of chemical research or large-scale manufacturing.

Future Prospects

Looking ahead, the story of 1-Bromo-3-chloropropane will likely shift with new priorities in chemical safety, sustainability, and targeted synthesis. Cleaner preparation methods—perhaps involving less hazardous reagents or step reductions—carry strong appeal, especially as environmental regulations tighten worldwide. Digital labs and in silico design techniques may help predict new uses or suggest novel derivatives tailored for pharmaceutical or electronic applications, spurring fresh research papers and patent filings. Calls for greener alternatives may one day push for biobased starting materials or substitute halogenated intermediates that offer lower toxicity without sacrificing usefulness. Realistically, as chemists keep pushing the boundaries of drug development, materials science, and agrochemical engineering, 1-Bromo-3-chloropropane remains a sturdy choice in the toolkit, ready to shape the next generation of custom molecules for industries that want to stay ahead in a competitive landscape.



What is 1-Bromo-3-Chloropropane used for?

Chemists in the Trenches

Years ago, during my first stint in a college chemistry lab, I watched as a bottle labeled “1-Bromo-3-Chloropropane” found its way across the workbench. Nobody paid it much attention—it looked like any ordinary clear liquid you might find in hundreds of labs. Even then, I saw how the little things moved big experiments forward. Later, I learned how this chemical means a great deal to scientists chasing accurate results in molecular biology and analytical chemistry.

Why This Compound Matters in DNA and RNA Work

Molecular biology isn’t all pipettes and petri dishes. Separating out DNA or RNA from a mash of proteins and fats takes tools that get the job done without extra baggage. Here, 1-Bromo-3-Chloropropane comes in as a phase separation reagent. Researchers spotted its knack for making extractions cleaner, particularly when traditional phenol and chloroform mixtures left lingering residues and brought along too much water in the wrong phase. The compound brings higher efficiency to isolating nucleic acids because it helps separate genetic material from contaminants better than other solvents in many protocols, like the famous Chomczynski-Sacchi method.

I’ve seen how stubborn some of these extractions can be. Inconsistent purity messes up everything down the line—PCR, sequencing, gene expression analysis. Data turns unreliable, experiments stall, and research budgets suffer. So when a chemical like 1-Bromo-3-Chloropropane improves that process, it frees up resources and time. Reports show this reagent often produces higher yields and cleaner separation, especially when handling high-fat or complex biological samples.

The Analytical Chemistry Edge

Lab work doesn’t stop at DNA. Analytical chemists use 1-Bromo-3-Chloropropane in sample preparation for gas chromatography—a go-to technique when mapping out volatile and semi-volatile compounds. Because of its properties, the compound works well as a solvent and helps isolate target compounds with less overlap and noise, translating to cleaner chromatograms and better quantitative results.

Safety Isn’t Just Talk

Anyone who’s uncapped a bottle of 1-Bromo-3-Chloropropane catches a whiff that demands respect. There’s a dark side to its usefulness—potential toxicity and environmental impact. This isn’t just a textbook concern. Exposure beyond recommended limits can irritate the skin, eyes, and respiratory tract. Extended handling needs proper gloves, goggles, and working hoods. The compound can linger in the environment, so disposal takes extra steps. Any decent lab safety officer will drill these things into your head.

I learned fast: treat every chemical as a potential hazard. Early in my lab days, a small spill led to a strong reprimand. Safety protocols exist for a reason, and 1-Bromo-3-Chloropropane is no exception. Laboratories using it need to train everyone thoroughly, enforce the use of ventilation, and work with local authorities to follow hazardous waste guidelines.

Room for Better Practices

Scientists keep searching for greener, safer methods, but right now, this compound occupies a necessary space in both molecular biology and analytical labs. The scientific community can work toward new extraction reagents or more sustainable alternatives that pose fewer risks. Sharing best practices, properly storing and disposing of chemicals, and investing in protective equipment lowers health and environmental impacts.

It’s easy to overlook these clear liquids tucked away on a shelf. Every vial matters, especially when it comes to precision, reproducibility, and safety. 1-Bromo-3-Chloropropane reminds us all that the backbone of modern research rests on careful choices in the lab, not just bold theories.

What are the safety precautions for handling 1-Bromo-3-Chloropropane?

Understanding the Hazards

1-Bromo-3-chloropropane looks like a simple clear liquid, but it packs more risk than most people think. This chemical does not carry a sharp smell to warn you of exposure, and the skin does not always tingle or burn after a small splash. That’s why too many lab workers drop their guard. Direct contact can cause skin irritation, and breathing in its vapor leaves you with headaches, coughing, or even dizziness. There are deeper risks here. 1-Bromo-3-chloropropane belongs to a group of alkyl halides, which many toxicologists flag as carcinogenic, mutagenic, or harmful to reproductive health. The fact is, careful handling is not just recommended—it’s necessary.

Gloves, Goggles, and Lab Coats Matter

Standing at a bench with an open vial of 1-Bromo-3-chloropropane, gloves often feel like a formality. I learned fast that nitrile gloves block out most accidental splashes, while latex or vinyl will break down too quickly with this kind of chemical. Splash goggles protect better than simple safety glasses, especially if you use a pipette or work with open containers. I’ve worked side-by-side with people who skip goggles. One tiny splash changed their view. A lab coat with closed cuffs keeps sleeves and skin covered. Handling this chemical in street clothes sets you up for trouble.

Respecting Ventilation

Working around volatile solvents always left me with one rule: call for good airflow. Fume hoods are your best tool in any room housing volatile or hazardous liquids. A basic bench near a window or with a small fan does not cut it. Vapors from 1-Bromo-3-chloropropane do not just drift away. Respiratory irritation creeps up if you let vapor linger. Routine work outside a certified hood means invisible risks to everyone in the room, not just the one handling the chemical.

Preventing Contamination and Spills

Leaving bottles or beakers uncapped, using old, cracked containers, or working near paper or cardboard spreads chemical droplets everywhere. Cross-contamination can show up days later. In the places where I’ve worked, lock-tight caps and double containment saved everyone plenty of headaches. For spills, absorbent pads, not paper towels, work best. I’ve seen small mistakes become big ones, especially when someone tries to clean a puddle with bare hands or tosses contaminated materials in regular trash.

Storage and Waste Disposal

1-Bromo-3-chloropropane asks for a cool, dry, and well-ventilated cabinet, away from acids or oxidizers. Riding out high temperatures or mixing it up with the wrong chemicals raises pressure or triggers violent reactions. Labeling every bottle sharply and keeping a spill kit nearby gives peace of mind. Waste collection containers need tight lids and clear hazard labels. Nothing cramps the flow of a busy lab like an accidental mix-up in chemical waste bins.

In Case of Exposure

Immediate washing with water, lots of it, makes all the difference for skin or eye contact. If someone breathes in vapor and feels faint, fresh air—and medical attention—come next. I never saw a story end well for someone who tried to “tough out” an exposure.

Building Safe Habits

Each time I see a lab safety checklist, I remember real stories of mishandled chemicals, close calls, and long-term effects from short-term slips. Treating 1-Bromo-3-chloropropane with respect means following every step, every time. Good habits protect not just the handler, but the whole workplace.

What is the molecular formula and structure of 1-Bromo-3-Chloropropane?

Knowing Your Chemical: Structure and Formula

I’ve spent years working in labs where every drop and every gram matter. Chemists, both in research and industry, handle all sorts of molecules—each one with unique traits. Give me a name, and I first see its structure in my mind. For 1-Bromo-3-Chloropropane, its molecular formula is C3H6BrCl. That spells out three carbons connected in a chain, with one end holding a bromine atom and the other end a chlorine atom.

Here’s how it looks in a simple sketch: Br–CH2–CH2–CH2–Cl. The bromine attaches to carbon number one; chlorine sits on carbon three. It doesn’t take a PhD to picture a straight, three-carbon backbone, with each terminal carbon claiming a different halogen. This sort of arrangement gives the molecule a direct, linear look.

Why Formula and Structure Matter

Anyone who’s spilled or mixed a reactive halogen compound understands their importance. Each slight change in positioning or element swap can shift a chemical’s entire character. In the world of organic chemistry, structure often trumps formula alone. Sure, the formula helps with calculations and inventory, but the true impact comes from the layout—the shape controlling reactivity, boiling point, and interactions with other compounds.

If you ask me why so many chemists keep meticulous notes, it’s the memory of reactions gone sideways. Even a simple swap, say, moving the chlorine from carbon three to carbon two, leads to a completely different set of possible reactions. These changes alter not just physical properties, but also what the molecule can build downstream.

Making Sense of Halogenated Compounds

Halogenated hydrocarbons look so innocent on paper, but handling them safely in a real workspace never gets old. I once worked on a project where the wrong isomer got mixed in; it looked right in the procurement form, but the difference showed up fast in the yield and purity checks. What’s been drilled into my head for years is that chemical identity starts with the details: which carbon connects to which group.

Working at the bench, you learn that the specific placement of bromine and chlorine anchors this molecule’s reactivity. That placement shapes what sorts of alkylations you can pull off, or what new pharmaceuticals or polymers these intermediates might help you assemble. These tools build the bigger molecules—no boring trivia there, just the foundation of chemistry as it works in labs and manufacturing plants worldwide.

Practices That Build Trust and Safety

On the job, no shortcut beats knowing exactly what’s in your bottle. Every responsible chemist double-checks structures rather than leaning on labels or outdated printouts. Misidentification isn’t just a nuisance; it breaks trust, wastes resources, and sometimes puts people at risk. The accurate molecular formula and structure stand as non-negotiable facts, not just for regulatory filings, but for safe and successful lab work. If you’re tracking your inventory or analyzing results, it all circles back to these basics.

The simple structure of 1-Bromo-3-Chloropropane reminds us that in chemistry, as in life, precision underpins real progress. From my own experience, taking care with each detail saves time, money, and even reputations.

How should 1-Bromo-3-Chloropropane be stored?

Getting Serious About Chemical Safety

Chemical storage sometimes feels like a routine job, but it can get personal fast if things go wrong. 1-Bromo-3-Chloropropane doesn't look threatening in its clear liquid form. Flip the bottle just once without care or miss a leak, and it reminds you that not all bottles in the lab play nice. This one sits firmly in the “handle with respect” camp thanks to its toxicity and volatility.

Understanding the Nature of the Chemical

Storing 1-Bromo-3-Chloropropane feels risky because it gives off harmful vapors and can irritate skin and eyes. Its boiling point hangs just above room temperature, which means it evaporates easily and its vapor could collect in low-lying places. A careless spill or cracked cap brings health hazards to everyone working nearby. Safe storage isn't about ticking boxes — it’s about walking into work tomorrow, knowing you protected yourself, your peers, and the environment.

Key Storage Practices That Actually Matter

Every lab worker hears “cool and dry” so often it sounds like white noise, but ignoring these words with this compound runs real risks. Shelving it anywhere near sources of ignition invites disaster. It’s flammable, and the simplest spark in the wrong place turns a forgettable afternoon into an actual emergency. That’s not a lesson anyone enjoys learning.

Keep it in a tightly sealed container made of a material that resists halogenated solvents — glass works well, but make sure the seal holds up, and that pressure doesn’t build inside. This isn’t just nitpicking: authorities like OSHA have reported workplace injuries caused by neglecting basic bottle checks. No one wants to open the storage, sniff something acrid, and realize protective gear should have been a priority.

Dedicated Storage Spaces: Not Optional

Throwing a hazardous compound on the regular chemical shelf breeds accidents. 1-Bromo-3-Chloropropane belongs in ventilated chemical storage cabinets, ideally ones rated for flammable materials. Don’t mix it with acids or bases — the reactions that follow don’t respect regular hours, and corrosion or fires almost always follow.

Separate from incompatible chemicals such as strong oxidizers. Ventilated cabinets with secondary containment trays catch drips, so a careless set-down or a fatigued end-of-day puts less at risk. Everyday habits make the biggest difference. Stash it below eye level if possible: one slip, and nobody wants a face full of toxic vapor.

Keeping Records Saves More Than Time

Anyone who’s lost track of an old solvent bottle knows the dread of finding it degraded, pressurized, or hanging open. Keep accurate logs and inspect every few weeks for signs of leaks or container breakdown. Date every bottle on arrival and disposal, then update the stock list. Quick access to current inventory matters a lot in emergencies or disposal audits.

Training: The Cornerstone of Safety

No storage trick replaces teaching people what this stuff does. Even a seasoned chemist learns something new every year about safe handling. Safety data sheets explain emergency steps, and practicing spill drills lowers panic levels the day a bottle slips. Every facility gains when newcomers absorb those lessons early and old hands refresh their memory often.

The Path Forward

Labs get busier, bottles fill shelves, and shortcuts tempt even careful people. 1-Bromo-3-Chloropropane brings out the need for discipline. Locking it up properly, checking containers, and training every hand that handles it lets science keep moving forward without unnecessary setbacks. Safe storage shapes lasting trust between teams — not just today, but for the long haul.

What are the physical and chemical properties of 1-Bromo-3-Chloropropane?

What You See and Smell

Looking at a bottle of 1-Bromo-3-Chloropropane gives a clear, colorless liquid—easy to mix with organic solvents but sinks below water’s surface. Its density, 1.53 grams per cubic centimeter at room temperature, means it feels heavier in the hand than most everyday liquids. I’ve handled it in a laboratory setting, and that sharp, sweet, almost ether-like odor leaves a mark in your memory. Gently swirling it in a vial brings out how easily it flows, with a viscosity that doesn’t slow down your work like more sluggish chemicals do.

Melting and Boiling—Points That Matter

1-Bromo-3-Chloropropane boils at about 142°C, which puts it far above water and many other solvents. This matters for anyone distilling or separating substances in a chemistry lab. The melting point sits around -72°C. Freezing it solid isn’t happening in any regular freezer, which opens useful windows for storage and mixing in colder spaces.

Chemical Personality: Stability, Reactivity, Safety

With halogens—bromine and chlorine—hanging off a propane backbone, this compound stands out as both a tool and a challenge for chemists. One thing that stands out: it's pretty stable under normal conditions. Yet, put it near strong bases or nucleophiles and it reacts, swapping out those halogen atoms in processes like nucleophilic substitution. That’s why it makes a handy intermediate for building bigger, more complex molecules. It also soaks up sunlight with a UV absorption below 250nm, giving labs another way to analyze or track what happens during reactions.

Now, safety calls for respect here. The same halogens that make it useful can irritate eyes, skin, and lungs. Nobody in a chemistry lab skips gloves and goggles around this compound. Spills need careful cleanup—the liquid can spread and the fumes can get into the air fast. Even the EPA takes this chemical seriously, tracking it because it won’t break down quickly in water or soil. People working near it know ventilation is a must.

Where Knowledge Meets Action

I’ve seen 1-Bromo-3-Chloropropane in action during extraction of nucleic acids—a task that depends on its ability to separate phases cleanly and efficiently. That density and immiscibility with water delivers results you can trust, whether you’re pulling DNA from tissues or prepping samples for sequencing in clinical labs.

Chemical production and industrial labs face real challenges with storage and disposal. Since the compound persists in the environment, it raises questions about sustainability and long-term safety. Setting up closed systems and recycling solvents can cut down on waste. For researchers, small-batch preparation and sourcing from trusted suppliers helps ensure purity and safety without stockpiling what you won’t use.

Better education about chemical handling makes a difference. I’ve taken part in training sessions that taught me the right way to store halogenated solvents and the best ways to contain spills. Sharing case studies, practicing emergency drills, and developing practical guides for safe chemical recycling could go a long way in supporting scientific progress while protecting people and the environment.

1-Bromo-3-Chloropropane
1-Bromo-3-Chloropropane
1-Bromo-3-Chloropropane
Names
Preferred IUPAC name 1-bromo-3-chloropropane
Other names 3-Bromopropyl chloride
Trimethylene bromochloride
1-Bromo-3-chloropropane
n-Propyl bromochloride
3-Chloropropyl bromide
Pronunciation /waɪˈbrəʊmoʊ θriː ˈklɔːroʊ prəˈpeɪn/
Identifiers
CAS Number 109-70-6
Beilstein Reference 657873
ChEBI CHEBI:41276
ChEMBL CHEMBL15440
ChemSpider 16706
DrugBank DB14241
ECHA InfoCard 03c54897-68fc-48ea-9ee6-9b061bfa963d
EC Number 208-059-9
Gmelin Reference 8092
KEGG C19589
MeSH D017718
PubChem CID 7916
RTECS number EK8575000
UNII 88HU93I5WP
UN number UN2688
Properties
Chemical formula C3H6BrCl
Molar mass 157.44 g/mol
Appearance Colorless to light yellow liquid
Odor sweet odor
Density 1.421 g/mL at 25 °C
Solubility in water slightly soluble
log P 1.98
Vapor pressure 2.1 mmHg (20°C)
Acidity (pKa) 14.6
Magnetic susceptibility (χ) -73.5×10⁻⁶ cm³/mol
Refractive index (nD) 1.464
Viscosity 1.613 cP (20°C)
Dipole moment 2.16 D
Thermochemistry
Std molar entropy (S⦵298) 353.7 J·mol⁻¹·K⁻¹
Std enthalpy of formation (ΔfH⦵298) -65.7 kJ·mol⁻¹
Std enthalpy of combustion (ΔcH⦵298) -545.1 kJ/mol
Pharmacology
ATC code Not assigned
Hazards
Main hazards Harmful if swallowed, causes skin and eye irritation, may cause respiratory irritation, suspected of causing cancer.
GHS labelling GHS02, GHS07
Pictograms GHS02,GHS07
Signal word Warning
Hazard statements H225, H302, H315, H319, H335
Precautionary statements P210, P280, P302+P352, P305+P351+P338, P403+P233
NFPA 704 (fire diamond) 1-2-0
Flash point 76 °F (24 °C)
Autoignition temperature 383 °C
Explosive limits Lower: 2.8% Upper: 16.8%
Lethal dose or concentration LD50 Oral Rat 2500 mg/kg
LD50 (median dose) LD50 (median dose): Oral rat LD50: 2800 mg/kg
NIOSH TX8575000
PEL (Permissible) Not established
REL (Recommended) 0.1 ppm
IDLH (Immediate danger) 200 ppm
Related compounds
Related compounds 1,3-Dibromopropane
1,3-Dichloropropane
1-Bromopropane
3-Chloropropan-1-ol
3-Bromopropan-1-ol
1-Chloropropane