Phytic Acid (~50percent in water)

For research use only. Not for therapeutic Use.

  • CAT Number: R053189
  • CAS Number: 83-86-3
  • Molecular Formula: C6H18O24P6
  • Molecular Weight: 660.04
  • Purity: ≥95%
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Phytic acid (~50% in water)(Cat No.:R053189)is a naturally occurring organic acid with six phosphate groups, commonly found in plant seeds as the principal storage form of phosphorus. In its aqueous solution form, it appears as a clear to slightly yellow liquid. This highly charged molecule chelates essential minerals such as calcium, iron, and zinc, making it both a potent antioxidant and an anti-nutrient in food science. It is widely used in cosmetics, pharmaceuticals, and agriculture for its chelating, preservative, and antioxidant properties. Proper storage is essential due to its hygroscopic and acidic nature.


CAS Number 83-86-3
Synonyms

myo-Inositol 1,2,3,4,5,6-Hexakis(dihydrogen phosphate); Alkalovert; Dermofeel PA 3; Exfoderm; Exfoderm Forte; Fytic Acid; IP6; Inositol 1,2,3,4,5,6-Hexakisphosphate; Inositol Hexakis(phosphate); Inositol hexaphosphate; InsP6; Phyliance; RP 3000; WHL;

Molecular Formula C6H18O24P6
Purity ≥95%
Target Xanthine Oxidase
IUPAC Name (2,3,4,5,6-pentaphosphonooxycyclohexyl) dihydrogen phosphate
InChI InChI=1S/C6H18O24P6/c7-31(8,9)25-1-2(26-32(10,11)12)4(28-34(16,17)18)6(30-36(22,23)24)5(29-35(19,20)21)3(1)27-33(13,14)15/h1-6H,(H2,7,8,9)(H2,10,11,12)(H2,13,14,15)(H2,16,17,18)(H2,19,20,21)(H2,22,23,24)
InChIKey IMQLKJBTEOYOSI-UHFFFAOYSA-N
SMILES C1(C(C(C(C(C1OP(=O)(O)O)OP(=O)(O)O)OP(=O)(O)O)OP(=O)(O)O)OP(=O)(O)O)OP(=O)(O)O
Reference

<p>
<span style=”color:#000000;”><span style=”font-family:arial,helvetica,sans-serif;”><span style=”font-size:12px;”>1.<span style=”font-variant-ligatures: normal; orphans: 2; widows: 2;”>Cheryan, Munir, and Joseph J. Rackis. &quot;Phytic acid interactions in food systems.&quot;&nbsp;</span><i style=”font-family: Arial, sans-serif; font-size: 13px; font-variant-ligatures: normal; orphans: 2; widows: 2;”>Critical Reviews in Food Science &amp; Nutrition</i><span style=”font-variant-ligatures: normal; orphans: 2; widows: 2;”>&nbsp;13.4 (1980): 297-335.<br />
2.</span><span style=”font-variant-ligatures: normal; orphans: 2; widows: 2;”>Oatway, Lori, Thava Vasanthan, and James H. Helm. &quot;Phytic acid.&quot;&nbsp;</span><i style=”font-family: Arial, sans-serif; font-size: 13px; font-variant-ligatures: normal; orphans: 2; widows: 2;”>Food Reviews International</i><span style=”font-variant-ligatures: normal; orphans: 2; widows: 2;”>&nbsp;17.4 (2001): 419-431.<br />
3.</span><span style=”font-variant-ligatures: normal; orphans: 2; widows: 2;”>Graf, Ernst, Katherine L. Empson, and Jone W. Eaton. &quot;Phytic acid. A natural antioxidant.&quot;&nbsp;</span><i style=”font-family: Arial, sans-serif; font-size: 13px; font-variant-ligatures: normal; orphans: 2; widows: 2;”>Journal of Biological Chemistry</i><span style=”font-variant-ligatures: normal; orphans: 2; widows: 2;”>&nbsp;262.24 (1987): 11647-11650.<br />
4.</span><span style=”font-variant-ligatures: normal; orphans: 2; widows: 2;”>Graf, Ernst. &quot;Applications of phytic acid.&quot;&nbsp;</span><i style=”font-family: Arial, sans-serif; font-size: 13px; font-variant-ligatures: normal; orphans: 2; widows: 2;”>Journal of the American Oil Chemists&rsquo; Society</i><span style=”font-variant-ligatures: normal; orphans: 2; widows: 2;”>&nbsp;60.11 (1983): 1861-1867.</span></span></span></span></p>

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