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15421-51-9

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15421-51-9 Usage

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.]

Check Digit Verification of cas no

The CAS Registry Mumber 15421-51-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,4,2 and 1 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 15421-51:
(7*1)+(6*5)+(5*4)+(4*2)+(3*1)+(2*5)+(1*1)=79
79 % 10 = 9
So 15421-51-9 is a valid CAS Registry Number.
InChI:InChI=1/C6H13O9P/c7-1-2(8)4(10)6(5(11)3(1)9)15-16(12,13)14/h1-11H,(H2,12,13,14)/t1-,2-,3-,4+,5-,6-/m1/s1

15421-51-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 1D-myo-inositol 1-phosphate

1.2 Other means of identification

Product number -
Other names 1D-myo-Inositol 1-monophosphate

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:15421-51-9 SDS

15421-51-9Relevant articles and documents

Ballou

, p. 99 (1962)

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

Seo, Kyung-Chang,Yu, Seok-Ho,Chung, Sung-Kee

, p. 305 - 327 (2008/02/12)

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

Kinetic resolution of d,l-myo-inositol derivatives catalyzed by chiral Cu(II) complex

Matsumura, Yoshihiro,Maki, Toshihide,Tsurumaki, Kazuya,Onomura, Osamu

, p. 9131 - 9134 (2007/10/03)

Kinetic resolution of d,l-myo-inositol derivatives having a 1,2-diol functionality by monobenzoylation was achieved using (R,R)-Ph-BOX-Cu(II) as a catalyst. The monobenzoylation preferentially took place at the 1,2-diol functionality via a highly enantiod

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