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All About 3-Bromophenol: Properties, Safety, and Why Chemists Love It (with a Few Caveats)

3-Bromophenol

3-Bromophenol Recommended Products

If you’re into chemistry, you’ve probably come across 3-Bromophenol. This little powerhouse is a go-to in industries like pharmaceuticals, agrochemicals, and research labs. But before you dive in, make sure you’re getting the good stuff. High-purity 3-Bromophenol is what you’re after. When shopping for it, look for suppliers that offer lab-grade or pharmaceutical-grade versions—no cutting corners here. Trust me, you’ll want that Certificate of Analysis (CoA) and Material Safety Data Sheets (MSDS) to confirm you’re dealing with the right product. It’s all about quality, people.

3-Bromophenol Properties

  • Molecular Formula: C6H4BrOH
  • CAS Number: 591-20-8
  • Molecular Weight: 173.00 g/mol
  • Melting Point: ~33°C (melty, but not too melty)
  • Boiling Point: ~235-236°C (pretty hot, right?)
  • Appearance: Colorless to pale yellow crystalline solid (kind of pretty, but don’t touch it).
  • Solubility: Sparingly soluble in water, but loves organic solvents like ethanol, chloroform, and ether.
  • Density: 1.63 g/cm³

This little molecule shines when you need to get into halogenation—perfect for reactions involving phenolic compounds. In short, it’s a must-have in synthetic chemistry.

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Here’s where it gets nerdy. Ever wonder how 3-Bromophenol stacks up against its cousins, 2-Bromophenol or 4-Bromophenol? It’s all about that bromine atom’s position on the ring. In 3-Bromophenol, the bromine hangs out at the meta-position. This positioning impacts how it reacts in the lab. Whether you need meta, ortho, or para positioning depends on what kind of magic you’re trying to work in your synthesis. Choose wisely.

3-Bromophenol Description

Let’s keep it simple: 3-Bromophenol is a 3- brominated phenol. With a bromine atom at the meta-position relative to the hydroxyl group, this compound is the definition of “small but mighty.” It’s your go-to intermediate for making everything from drugs to agrochemicals to dyes. Plus, it’s a favorite in research because of its role in exploring new substitution reactions and helping chemists cook up fresh compounds.

3-Bromophenol General Description

In the lab, 3-Bromophenol is all about electrophilic substitution. Its bromine atom increases reactivity, making it perfect for creating brominated aromatic compounds. It’s a chemical jack-of-all-trades—used in everything from drug development to making dyes and pesticides. If you’re in the research game, 3-Bromophenol helps you get to the bottom of how halogenated phenols behave. Spoiler: They’re pretty fascinating.

Safety Information

Heads up! This isn’t the kind of compound you want to mess around with. 3-Bromophenol can be harmful to your health and the environment. Your best bet is to always read the Material Safety Data Sheet (MSDS) that comes with it. Trust me, it’s not light reading, but it’s important.

Pictograms

  • Irritant: Yep, it can irritate your skin, eyes, and respiratory system. Fun times.
  • Environmental Hazard: Not to be dramatic, but it’s toxic to aquatic life. Keep it far, far away from the fish.

Signal Word

The label here is “Warning”. Translation? Handle with care, or things could get uncomfortable.

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Hazard Statements

  • H315: Skin irritation alert!
  • H319: Your eyes won’t like it either.
  • H335: Breathing it in? Not a great idea.
  • H411: Remember the fish? Yeah, still not good for them.

Precautionary Statements

  • P261: Don’t go inhaling this stuff. Seriously.
  • P280: Gloves, goggles, and a lab coat—your new best friends.
  • P273: Let’s keep this chemical away from rivers, lakes, and oceans, okay?
  • P305+P351+P338: If it gets in your eyes, rinse. Rinse. Rinse. And maybe ditch the contacts for a bit.

Take these warnings seriously to avoid an accidental chemistry horror story.

Hazard Classifications

In a nutshell, 3-Bromo phenol isn’t something to play with. It’s classified as:

  • Acute Toxicity (Category 4): Not fatal, but you definitely don’t want to test that.
  • Skin Irritation (Category 2): Expect some redness if it gets on you.
  • Serious Eye Damage/Eye Irritation (Category 2A): Your eyes will not thank you.
  • Aquatic Chronic Toxicity (Category 2): Again with the fish—not a fan.

Peer-Reviewed Papers

If you want to geek out a bit more, 3 Bromophenol has made the rounds in academic circles. Researchers have used it in a ton of synthesis studies, figuring out how to make even more complex compounds. It’s also been studied for its pharmaceutical potential—think anti-cancer and anti-inflammatory agents. And don’t forget the environmental impact papers: scientists are looking into just how toxic brominated phenols are to our ecosystems. (Spoiler: Pretty toxic.)

Conclusion

All in all, 3-Bromophenol is like the Swiss army knife of the chemistry world. Whether you’re making drugs, dyes, or pesticides, it’s a compound that delivers. But—and this is a big but—make sure you know what you’re doing and protect yourself. This stuff might be powerful, but it comes with a few strings attached. Handle with care, and you’ll be able to take full advantage of its capabilities without any unexpected lab mishaps

FAQ

What is the density of 3 bromophenol?

The density of 3-Bromophenol is 1.49 g/cm³.

What is an alternative name for 3-bromophenol?

An alternative name for 3-Bromophenol is m-Bromophenol. The “m” stands for “meta,” indicating the position of the bromine atom relative to the hydroxyl group on the benzene ring.

What is the formula for 3-bromophenol?

The formula for 3-Bromophenol is C6H5BrO.

What is the charge of bromophenol?

Bromophenol blue has a slight negative charge and will migrate the same direction as DNA, allowing the user to monitor the progress of molecules moving through the gel. The rate of migration varies with gel composition.

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