69256-52-6

Basic information

• Product Name: D-myo-Inositol 4-monophosphate ammonium salt
• Synonyms: D-MYO-INOSITOL 4-MONOPHOSPHATE AMMONIUM SALT
• CAS NO: 69256-52-6
• Molecular Formula: C₆H₁₃O₉P
• Molecular Weight: 294.2
• Mol File: 69256-52-6.mol
• Article Data: 16

Chemical Properties

• Appearance: /
• Storage Temp.: ?20°C
• CAS DataBase Reference: D-myo-Inositol 4-monophosphate ammonium salt(CAS DataBase Reference)
• NIST Chemistry Reference: D-myo-Inositol 4-monophosphate ammonium salt(69256-52-6)
• EPA Substance Registry System: D-myo-Inositol 4-monophosphate ammonium salt(69256-52-6)

Safety Data

• Hazardous Substances Data: 69256-52-6(Hazardous Substances Data)

Upstream product

• 441311-55-3 2-O-phosphono-1,3,4,5,6-penta-O-acetyl-myo-inositol 
• 87-89-8 D-myo-inositol 
• 75194-94-4 3,3,7,7-tetramethyl-2,8-dioxa-5-aza-1λ³-phosphabicyclo(3,3,0)octane 
• 125288-06-4 4,6-di-O-benzyl-myo-inositol 2-dibenzylphosphate 
• 26326-85-2 Ins(1,2,3,4,6)P5 
• 26326-86-3 Ins(1,2,3,4,5)P₅ 
• 114418-96-1 Ins(1,2,4,5,6)P₅ 
• 864372-89-4 1,4,5-tri-O-acetyl-3,6-di-O-benzyl-2-O-(3-oxo-1,5-dihydro-3λ⁵-2,4,3-benzodioxaphosphepin-3-yl)-D-myo-inositol 
• 864372-74-7 (1S,2R,3R,4S)-2,3-di-O-acetyl-1,4-di-O-benzylconduritol B 
• 864372-76-9 4,5-di-O-acetyl-3,6-di-O-benzyl-D-myo-inositol 
• 864372-88-3 1,4,5-tri-O-acetyl-3,6-di-O-benzyl-D-myo-inositol 
• 864372-83-8 2,4,5-tri-O-acetyl-3,6-di-O-benzyl-D-myo-inositol 
• 98510-20-4 myo-Inositol orthoformate 
• 120268-33-9 4/6-O-benzyl-myo-inositol 1,3,5-monoorthoformate 

Downstream Products

• 33608-52-5 DL-O¹,O²-hydroxyphosphoryl-myo-inositol 
• 551-72-4 inositol 
• 86119-84-8 phosphoric acid 

Relevant articles and documents

Divergent synthesis of all possible optically active regioisomers of myo-inositol mono- and bisphosphates

All possible optically active regioisomers of myo-inositol mono- and bisphosphates were synthesized using inositol derivatives suitably protected with various protecting groups (IRns) as key intermediates. A series of procedures including Novozym 435 cata

Flexible stereo- and regioselective synthesis of myo-inositol phosphates (part 1): Via symmetrical conduritol B derivatives

A practical route is described for the preparation of myo-inositol polyphosphates. Optically pure myo-inositol derivatives can be prepared from p-benzoquinone in both forms by enzymatic resolution of a C2- symmetric diacetoxyconduritol B key in

Pathway of dephosphorylation of myo-inositol hexakisphosphate by phytases of legume seeds

Using a combination of high-performance ion chromatography analysis and kinetic studies, the pathway of dephosphorylation of myo-inositol hexakisphosphate by the phytases purified from faba bean and lupine seeds, respectively, was established. The data demonstrate that the legume seed phytases under investigation dephosphorylate myo-inositol hexakisphosphate in a stereospecific way. The phytase from faba bean seeds and the phytase LP2 from lupine seeds degrade phytate by sequential removal of phosphate groups via D-Ins(1,2,3,5,6)P5, D-Ins(1,2,5,6)P4, D-Ins(1,2,6)P3, and D-Ins(1,2)P2 to finally Ins(2)P, whereas the phytases LP11 and LP12 from lupine seeds generate the final degradation product Ins(2)P via D-Ins(1,2,4,5,6)P5, D-Ins(1,2,5,6)P4, D-Ins(1,2,6)P3, and D-Ins(1,2)P2.