ChemicalBook >> CAS DataBase List >>[(2S,3R,5S,6S)-2,3,4,5,6-pentahydroxycyclohexyl]oxyphosphonic acid

[(2S,3R,5S,6S)-2,3,4,5,6-pentahydroxycyclohexyl]oxyphosphonic acid

CAS No.
15421-51-9
Chemical Name:
[(2S,3R,5S,6S)-2,3,4,5,6-pentahydroxycyclohexyl]oxyphosphonic acid
Synonyms
Inositol phosphate;inositol 1-phosphate;Inositol 1-monophosphate;1D-myo-inositol 1-phosphate;D-Myo-inositol, 1-(dihydrogen phosphate);[(2S,3R,5S,6S)-2,3,4,5,6-pentahydroxycyclohexyl]oxyphosphonic acid
CBNumber:
CB21236028
Molecular Formula:
C6H13O9P
Molecular Weight:
260.14
MDL Number:
MOL File:
15421-51-9.mol
Last updated:2023-05-04 17:34:34

[(2S,3R,5S,6S)-2,3,4,5,6-pentahydroxycyclohexyl]oxyphosphonic acid Properties

Boiling point 517.4±60.0 °C(Predicted)
Density 2.02±0.1 g/cm3(Predicted)
pka 1.91±0.10(Predicted)

[(2S,3R,5S,6S)-2,3,4,5,6-pentahydroxycyclohexyl]oxyphosphonic acid Chemical Properties,Uses,Production

Definition

ChEBI: 1D-myo-inositol 1-phosphate is an inositol having myo- configuration substituted at position 1 by a phosphate group. It has a role as a human metabolite, an Escherichia coli metabolite and a mouse metabolite. It is functionally related to a myo-inositol. It is a conjugate acid of a 1D-myo-inositol 1-phosphate(2-).

Agricultural Uses

Inositol, a cyclic molecule with six hydroxyl groups, forms the hydrophobic head group of membrane inositol phospholipids. Inositol phosphates are intracellular second messengers in eukaryotic cells. The most studied of them is inositol1,4,5 triphosphate (IP3) which is said to play an important role in releasing calcium ions from intracellulars tores in endoplasmic reticulum.
Inositol phosphate is considered to be of microbial origin and its various forms are characterized in soil. It can exist in several stereoisomeric forms (a isomeric forms) such as myo, scyllo, neo and chrio.
Inositol hexaphosphoric acid, known as phytic acid, occurs in nature in the seeds of many cereal grains as insoluble calcium or magnesium salts. It inhibits the absorption of calcium in the intestine.

Purification Methods

Crystallise the phosphate from water, and EtOH. Recrystallise 1g by dissolving it in 3mL of H2O and adding slowly 15mL of commercial EtOH, filter the crystals, wash with a little EtOH then Et2O and dry it in a vacuum. [McCormick & Carter Biochemical Preparations 2 65 1952.]

[(2S,3R,5S,6S)-2,3,4,5,6-pentahydroxycyclohexyl]oxyphosphonic acid Preparation Products And Raw materials

Raw materials

Preparation Products

Global( 7)Suppliers
Supplier Tel Email Country ProdList Advantage
Hubei Jusheng Technology Co.,Ltd.
18871490254 linda@hubeijusheng.com CHINA 28180 58
ShenZhen Trendseen Biological Technology Co.,Ltd.
13417589054 trendseenbio@gmail.com China 11681 58
Amadis Chemical Company Limited
571-89925085 sales@amadischem.com China 131981 58
BOC Sciences 1-631-485-4226; 16314854226 info@bocsci.com United States 14059 65
BOC Sciences 16314854226 info@bocsci.com United States 9926 65
Shanghai Yiyan Biotechnology Co. , Ltd. 021-69985186 13611928337 3427709316@qq.com China 7984 58
ShenZhen Trendseen Biological Technology Co.,Ltd. 13417589054 13417589054 trendseenbio@gmail.com China 8941 58
[(2S,3R,5S,6S)-2,3,4,5,6-pentahydroxycyclohexyl]oxyphosphonic acid Inositol phosphate inositol 1-phosphate D-Myo-inositol, 1-(dihydrogen phosphate) Inositol 1-monophosphate 1D-myo-inositol 1-phosphate 15421-51-9 Elisa Kit-Mouse Elisa Kit