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L-INS(1,4,5)P3, 6K is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 129828-71-3 Structure
  • Basic information

    1. Product Name: L-INS(1,4,5)P3, 6K
    2. Synonyms: L-MYO-INOSITOL 1,4,5-TRIPHOSPHATE HEXAPOTASSIUM SALT;L-MYO-INOSITOL 1,4,5-TRISPHOSPHATE 6K;L-MYO-INOSITOL 1,4,5-TRISPHOSPHATE, HEXAPOTASSIUM SALT;L-MYO-INOSITOL 1,4,5-TRIS-PHOSPHATE POTASSIUM SALT;L-MYO-INS(1,4,5)P3 6K;L-INS(1,4,5)P3, 6K;L-myo-inositol 1,4,5-tris-*phosphate potassium
    3. CAS NO:129828-71-3
    4. Molecular Formula: C6H9O15P3*6K
    5. Molecular Weight: 648.64
    6. EINECS: N/A
    7. Product Categories: Carbohydrates;Carbohydrates A to;Carbohydrates H-LBiochemicals and Reagents;Monosaccharide
    8. Mol File: 129828-71-3.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: −20°C
    8. Solubility: N/A
    9. CAS DataBase Reference: L-INS(1,4,5)P3, 6K(CAS DataBase Reference)
    10. NIST Chemistry Reference: L-INS(1,4,5)P3, 6K(129828-71-3)
    11. EPA Substance Registry System: L-INS(1,4,5)P3, 6K(129828-71-3)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany: 3
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 129828-71-3(Hazardous Substances Data)

129828-71-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 129828-71-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,9,8,2 and 8 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 129828-71:
(8*1)+(7*2)+(6*9)+(5*8)+(4*2)+(3*8)+(2*7)+(1*1)=163
163 % 10 = 3
So 129828-71-3 is a valid CAS Registry Number.
InChI:InChI=1/C6H15O15P3.6K/c7-1-2(8)5(20-23(13,14)15)6(21-24(16,17)18)3(9)4(1)19-22(10,11)12;;;;;;/h1-9H,(H2,10,11,12)(H2,13,14,15)(H2,16,17,18);;;;;;/q;6*+1/p-6/t1-,2+,3+,4-,5-,6-;;;;;;/m0....../s1

129828-71-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1D-myo-inositol 1,3,4-triphosphate hexapotassium salt

1.2 Other means of identification

Product number -
Other names L-INS(1,4,5)P3, 6K

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:129828-71-3 SDS

129828-71-3Downstream Products

129828-71-3Relevant articles and documents

An efficient chemoenzymic access to optically active myo-inositol polyphosphates

Gou,Liu,Chen

, p. 51 - 64 (2007/10/02)

The 1,4,5-tris-, 1,3,4-tris-, and 1,3,4,5-tetrakis-phosphates of 1D-myo-inositol have been prepared in their enantiomerically pure forms from the two enantiomers of 1,2:5,6-di-O-cyclohexylidene-myo-inositol. A facile enzymic preparation is also described

Synthesis and Some Properties of D-myo-Inositol 1,4,5-Tris(dihydrogen phosphate)

Ozaki, Shoichiro,Kondo, Yoshihisa,Shiotani, Naokazu,Ogasawara, Tomio,Watanabe, Yutaka

, p. 729 - 738 (2007/10/02)

Optically active myo-inositol 1,4,5-tris(dihydrogen phosphate) 1, which has now been recognized as a second messenger in a new intracellular signal transduction system, has been prepared starting from myo-inositol.The key step, phosphorylation of an adequately protected polyhydroxy derivative, was accomplished by three methods, among which a phosphoramidite method using a new phosphitylating agent, o-xylylene N,N-diethylphosphoramidite, gave the triphosphoric ester in quantitative yield.Optical resolution was effectively realized by derivatization into diastereoisomeric l-menthoxyacetic esters.NMR spectra and optical rotation are shown to depend on the pH of an aqueous solution of compound 1.

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