DL-Myo-Inositol 1,4,5-Tris(dihydrogen Phosphate) HexaaMMoniuM Salt

Base Information

Chemical Name:DL-Myo-Inositol 1,4,5-Tris(dihydrogen Phosphate) HexaaMMoniuM Salt
CAS No.:112571-68-3
Molecular Formula:C₆H₉O₁₅P₃*6H₄N
Molecular Weight:522.28
Hs Code.:
Mol file:112571-68-3.mol

Synonyms:DL-Myo-Inositol 1,4,5-Tris(dihydrogen Phosphate) HexaaMMoniuM Salt;DL-Myo-Inositol 1,4,5-Trisphosphate HexaaMMoniuM Salt

Suppliers and Price of DL-Myo-Inositol 1,4,5-Tris(dihydrogen Phosphate) HexaaMMoniuM Salt

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Usbiological
DL-myo-Inositol 1,4,5-Trisphosphate Hexaammonium Salt
5mg
$ 460.00

TRC
DL-myo-Inositol1,4,5-TrisphosphateHexaammoniumSalt
1mg
$ 165.00

Medical Isotopes, Inc.
DL-myo-Inositol1,4,5-TrisphosphateHexaammoniumSalt
50 mg
$ 2200.00

Total 3 raw suppliers

Chemical Property of DL-Myo-Inositol 1,4,5-Tris(dihydrogen Phosphate) HexaaMMoniuM Salt

Chemical Property:

PSA：309.84000
LogP:-1.54020

Purity/Quality:

99% ^*data from raw suppliers

DL-myo-Inositol 1,4,5-Trisphosphate Hexaammonium Salt ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Uses Inositol 1,4,5-trisphosphate receptors (IP3R) are expressed in almost all animal cells. They control the release of Ca2+ ions useful in the regulation of Ca2+ signalling system, dysregulation of which has been linked to many diseases such as cardiac disease, schizophrenia, bipolar disorder and Alzheimer''s disease. DL-Myo-Inositol 1,4,5-Tris(dihydrogen Phosphate) Hexaammonium Salt is expressed in almost all animal cells. They control the release of Ca2+ ions useful in the regulation of Ca2+ signalling system, dysregulation of which has been linked to many diseases such as cardiac disease, schizophrenia, bipolar disorder and Alzheimer's disease.

Technology Process of DL-Myo-Inositol 1,4,5-Tris(dihydrogen Phosphate) HexaaMMoniuM Salt

There total 32 articles about DL-Myo-Inositol 1,4,5-Tris(dihydrogen Phosphate) HexaaMMoniuM Salt which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 100.0%

: Acetic acid (1S,2R,3R,4S,5R,6R)-3,4-dihydroxy-2,5,6-tris-phosphonooxy-cyclohexyl ester

: 112571-68-3,112571-69-4,116183-54-1,127910-79-6,127910-80-9,129704-99-0,129828-70-2,141611-09-8
D-myo-inositol 1,4,5-triphosphate ammonium salt

Guidance literature:: With ammonium hydroxide; Ambient temperature;
DOI:10.1016/0008-6215(94)84226-4

Reference yield:

: 87-89-8
D-myo-inositol

: 112571-68-3,112571-69-4,116183-54-1,127910-79-6,127910-80-9,129704-99-0,129828-70-2,141611-09-8,345958-55-6
D-myo-inositol 1,3,4-triphosphate

Guidance literature:: Multi-step reaction with 11 steps

1: p-toluenesulfonic acid

2: 94 percent / sodium hydride / dimethylformamide

3: 66 percent / I₂, / methanol

4: 86 percent / sodium hydride / dimethylformamide / 2 h / 60 °C

5: 0.1 M hydrogen chloride / methanol

6: 81 percent / dibutyltinoxide

7: 97 percent / sodium hydride / dimethylformamide / 2 h / 60 °C

8: 86 percent / DDQ

9: 80 percent / 0.1 M hydrogen chloride / methanol

10: 70 percent / butyllithium

11: hydrogen / 5 percent Pd/C / 24 h / Ambient temperature

With hydrogenchloride; n-butyllithium; hydrogen; iodine; sodium hydride; di(n-butyl)tin oxide; toluene-4-sulfonic acid; 2,3-dicyano-5,6-dichloro-p-benzoquinone; palladium on activated charcoal; In methanol; N,N-dimethyl-formamide;
DOI:10.1246/cl.1988.77

Reference yield:

: 6763-49-1,23393-19-3,33021-17-9,34361-61-0,34395-04-5,34711-26-7,40773-57-7,41545-19-1,54712-58-2,57089-24-4,57089-25-5,68738-25-0,81601-23-2,120710-65-8,141506-87-8
(+/-)-1,2:5,6-dicyclohexylidene-myo-inositol

: 112571-68-3,112571-69-4,116183-54-1,127910-79-6,127910-80-9,129704-99-0,129828-70-2,141611-09-8,345958-55-6
D-myo-inositol 1,3,4-triphosphate

Guidance literature:: Multi-step reaction with 10 steps

1: 94 percent / sodium hydride / dimethylformamide

2: 66 percent / I₂, / methanol

3: 86 percent / sodium hydride / dimethylformamide / 2 h / 60 °C

4: 0.1 M hydrogen chloride / methanol

5: 81 percent / dibutyltinoxide

6: 97 percent / sodium hydride / dimethylformamide / 2 h / 60 °C

7: 86 percent / DDQ

8: 80 percent / 0.1 M hydrogen chloride / methanol

9: 70 percent / butyllithium

10: hydrogen / 5 percent Pd/C / 24 h / Ambient temperature

With hydrogenchloride; n-butyllithium; hydrogen; iodine; sodium hydride; di(n-butyl)tin oxide; 2,3-dicyano-5,6-dichloro-p-benzoquinone; palladium on activated charcoal; In methanol; N,N-dimethyl-formamide;
DOI:10.1246/cl.1988.77