Reciprocal Net Site sponsor
   Site Info    |    Search
Common molecules sample 50904 - Reciprocal Net Log in
You will need to download and install a Java plug-in in order to view this applet. Download Sun's Java plug-in from here.

Switch to another visualization applet:

> miniJaMM open in new window...
- JaMM1
- JaMM2
Empirical formula: C1H2O2
a: 10.230 Å
b: 3.640 Å
c: 5.340 Å
α (alpha): 90.00 °
β (beta): 90.00 °
γ (gamma): 90.00 °
Volume: 198.85 Å3
Space group: Pna21
Calculated density: 1.537 g/cm3
Z: 4
Temperature: -175.0 °C
Formula weight: 46.026 g/mole
R(F): 0.0980
Structural formula: C1H2O2
Common name: Formic acid
Keyword: fumigant
Keyword: organic acid
Short description: Formic acid is a colorless liquid with a pungent and penetrating odor with a sour taste.
CSD refcode: FORMAC
Citation of a publication: F. Holtzberg, B. Post, I. Fankuchen; Acta Crystallogr., 6, (1953), 127.
Layman's explanation: Formic Acid, also known as methanoic acid and hydrogencarboxylic acid, is the simplest organic acid. It is a colorless, toxic, corrosive liquid with a pungent, penetrating odor. In nature, it is found in the stings and bites of many insects of the order hymenoptera, including bees and ants. The principal use of formic acid is as a preservative and antibacterial agent in livestock feed. The largest single use of formic acid is as a silage additive in Europe, but this market hardly exists in the United States. When sprayed on fresh hay or other silage, it arrests certain decay processes and causes the feed to retain its nutritive value longer. In the poultry industry, it is sometimes added to silage to kill salmonella bacteria. It is also used in textile dyeing, leather tanning, as a solvent, in electroplating processes, in the manufacturing of lacquers, glass, vinyl resin plasticizers, and formate esters (for flavor and fragrance) and in the manufacture of fumigants. Formic acid is a strong reducing agent, and may act both as an acid and as an aldehyde because the carboxyl is bound to a hydrogen rather than an alkyl group.
Lab name: Common molecules
Sample provider: Obtained courtesy of the Cambridge Structural Database
Status: Complete, visible to public
Repository Files:
50904.cif 50904.crt 50904.GIF 50904.ort 50904.pdb
50904.sdt

Reciprocal Net site software 0.9.1-50, copyright (c) 2002-2009, The Trustees of Indiana University
Files and data presented via this software are property of their respective owners.
Reciprocal Net is funded by the U.S. National Science Foundation as part of the National Science Digital Library project. NSDL