Seed Media Group

Search this blog

Profile

Molecules: You'd better learn to live with them.

Recent Posts

Recent Comments

Archives

Blogroll

Other Information


The author is not a physician. The content on this website does not, and is not intended to constitute medical advice. It should not be relied upon when making medical decisions. It is not intended as a substitute for advice from your physician or other healthcare provider.

« Diethyl pyrocarbonate/DEPC (Making the world safe for RNA everywhere) | Main | Havidol Redux »

Ammonium carbonate (Stinky leavening)

Category: Stinky
Posted on: February 23, 2007 9:08 PM, by Molecule of the Day

Ammonium carbonate is analogous to the other bicarbonate and carbonate salts you see - baking soda. In the presence of acid; or just sufficient heat, it will offgas ammonia and carbon dioxide, hopefully leaving pleasing bubbles in whatever you're making.

InChI=1/CH2O3.2H3N/c2-1(3)4;;/h(H2,2,3,4);2*1H3

Whatever you're making better not have much moisture, though. Ammonia loves water, and any residual water will hold onto enough to give whatever food you're making a profound stench. This pretty much limits you to crackers; ammonium carbonate-leavened banana bread will not be pleasant.

The salt has been around for a long time but has been supplanted almost entirely by baking soda (sodium bicarbonate, NaHCO3), which adds a little sodium to the recipe but has the distinct advantage of not imparting the taste of kitchen cleaner to your cupcakes.

TrackBacks

TrackBack URL for this entry:

Comments

The strange thing about the smell of ammonia is that on its own it is quite pleasant in small doses (at least in my opinion) but when it is combined with anything else it smells foul.
For instance if you are precipitating protein from fish guts with ammonium sulfate it smells horribly rancid even though the fish is fresh and not bad smelling when you begin.

Posted by: oskar | February 25, 2007 8:13 AM

I maintain that thiols smell worse...

but that's a whole different stinky issue...

Posted by: Mark C R UK | February 26, 2007 10:58 AM

I thought "ammonium carbonate" was actually ammonium carbamate, NH2COO- NH4+. When a strong primary amine, such as ethyl 3-aminopropionate reacts with air it forms RNHCOO-NH4-R and not (RNH3)2 CO3. The nmr spectrum clearly shows that the salt is a carbamate salt and not a carbonate.

Posted by: Howard McPherson | March 6, 2007 5:31 PM

Post a Comment

(Email is required for authentication purposes only. Comments are moderated for spam, your comment may not appear immediately. Thanks for waiting.)





Having problems commenting?

Search All Blogs

Blogs in the Network

Top Five: Most German

Top Science Stories

powered by SEED - seedmagazine.com