Traumatic acid

Traumatic acid[1]
Names
IUPAC name
Dodec-2-enedioic acid
Other names
trans-Traumatic acid
Identifiers
6402-36-4 YesY
3D model (Jmol) Interactive image
ChEMBL ChEMBL470062 N
ECHA InfoCard 100.026.382
PubChem 5283028
Properties
C12H20O4
Molar mass 228.28
Melting point 166 to 167 °C (331 to 333 °F; 439 to 440 K)
Boiling point 150 to 160 °C (302 to 320 °F; 423 to 433 K) at 0.001 mmHg
Sparingly soluble
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
N verify (what is YesYN ?)
Infobox references

Traumatic acid is a monounsaturated dicarboxylic acid naturally occurring in plants. The compound was first isolated from wounded bean plants by American chemists James English Jr. and James Frederick Bonner and Dutch scientist Arie Jan Haagen-Smit in 1939.[2] Traumatic acid is a potent wound healing agent in plants ("wound hormone") that stimulates cell division near a trauma site to form a protective callus and to heal the damaged tissue. It may also act as a growth hormone, especially in inferior plants (e.g. algae). Traumatic acid is biosynthesized in plants by non-enzymatic oxidation of traumatin (12-oxo-trans-10-dodecenoic acid), another wound hormone.

At normal conditions, traumatic acid is a solid, crystalline, water-insoluble substance. The salts and esters of traumatic acid are called traumatates.

Traumatic acid is used as an intermediate in prostaglandin synthesis. It is also a constituent of some pharmaceutical products, such as the odontostomatologic gel Restomyl, due to its mucosal re-epithelialization activity.

References

  1. Merck Index, 11th Edition, 9493
  2. English J Jr., Bonner J, Haagen-Smit AJ: Structure and synthesis of a plant wound hormone. Science 90:329. (1939)
This article is issued from Wikipedia - version of the 9/28/2015. The text is available under the Creative Commons Attribution/Share Alike but additional terms may apply for the media files.