Psyllic acid

From Infogalactic: the planetary knowledge core
Jump to: navigation, search
Psyllic acid
250px
Names
IUPAC name
Tritriacontanoic acid
Identifiers
38232-03-0 YesY
ChemSpider 157945 N
Jmol 3D model Interactive image
PubChem 181572
  • InChI=1S/C33H66O2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20-21-22-23-24-25-26-27-28-29-30-31-32-33(34)35/h2-32H2,1H3,(H,34,35) N
    Key: HQRWEDFDJHDPJC-UHFFFAOYSA-N N
  • InChI=1/C33H66O2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20-21-22-23-24-25-26-27-28-29-30-31-32-33(34)35/h2-32H2,1H3,(H,34,35)
    Key: HQRWEDFDJHDPJC-UHFFFAOYAH
  • O=C(O)CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC
Properties
C33H66O2
Molar mass 494.89 g·mol−1
Vapor pressure {{{value}}}
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

Psyllic acid (also pysslostearic acid, tritriacontanoic acid or ceromelissic acid) is a saturated fatty acid.

Alkali salts

The alkali salts of psyllic acid are precipitated when alcoholic solutions of the acid and an alkali hydroxide are mixed. The silver and barium salts can be obtained by adding aqueous alcoholic solutions of silver nitrate and barium chloride to alcoholic solutions of the acid. The following salts have been analyzed: C38H65O2Na, C66H130O4Ba, and C33H65O2Ag. Psylla wax is hydrolyzed by alcoholic potassium hydroxide as well as by hydrobromic acid.[1][2]

Nutritional sources

Psyllic acid is present in Chinese wolfberries.[3][4]

See also

References

  1. Lua error in package.lua at line 80: module 'strict' not found.
  2. Psylla Wax. IV. Psyllic Acid and its Salts. Ernst E. Sundvik (Zeitsch. physiol. Chem., 1908, 54, 255-257. Compare Abstr., 1898, i, 617; 1901, i, 358; 190, i, 887)
  3. Lua error in package.lua at line 80: module 'strict' not found.
  4. Lua error in package.lua at line 80: module 'strict' not found.

External links