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Zinc pivalate, also known as zinc 2,2-dimethylpropanoate, is a chemical compound with the formula Zn(C5H9O2)2. It is a white powder that is primarily used in the pharmaceutical industry as an intermediate for the synthesis of various drugs.

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  • 15827-10-8 Structure
  • Basic information

    1. Product Name: zinc pivalate
    2. Synonyms: zinc pivalate;zinc:2,2-dimethylpropanoate
    3. CAS NO:15827-10-8
    4. Molecular Formula: C10H18O4Zn
    5. Molecular Weight: 267.63752
    6. EINECS: 239-929-3
    7. Product Categories: N/A
    8. Mol File: 15827-10-8.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 166.2°Cat760mmHg
    3. Flash Point: 68.3°C
    4. Appearance: /
    5. Density: g/cm3
    6. Vapor Pressure: 0.907mmHg at 25°C
    7. Refractive Index: N/A
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: zinc pivalate(CAS DataBase Reference)
    11. NIST Chemistry Reference: zinc pivalate(15827-10-8)
    12. EPA Substance Registry System: zinc pivalate(15827-10-8)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 15827-10-8(Hazardous Substances Data)

15827-10-8 Usage

Uses

Used in Pharmaceutical Industry:
Zinc pivalate is used as a pharmaceutical intermediate for the synthesis of various drugs. Its application in this industry is due to its ability to serve as a building block for the development of new medications, contributing to the advancement of pharmaceutical research and drug discovery.
As a white powder, zinc pivalate's physical properties make it suitable for use in the pharmaceutical industry, where it can be easily incorporated into various formulations and processes. Its role as an intermediate allows for the creation of a wide range of pharmaceutical products, ultimately benefiting the healthcare sector and patients in need of effective treatments.

Check Digit Verification of cas no

The CAS Registry Mumber 15827-10-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,8,2 and 7 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 15827-10:
(7*1)+(6*5)+(5*8)+(4*2)+(3*7)+(2*1)+(1*0)=108
108 % 10 = 8
So 15827-10-8 is a valid CAS Registry Number.
InChI:InChI=1/C5H10O2.Zn/c1-5(2,3)4(6)7;/h1-3H3,(H,6,7);/q;+2/p-1

15827-10-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name zinc,2,2-dimethylpropanoate

1.2 Other means of identification

Product number -
Other names Propanoic acid,2,2-dimethyl-,zinc salt (2:1)

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:15827-10-8 SDS

15827-10-8Downstream Products

15827-10-8Relevant articles and documents

Synthesis of bis- and tris-organophosphorus substituted amines and amino acids with PCH2N Fragments

Prishchenko, Andrey A.,Livantsov, Mikhail V.,Novikova, Olga P.,Livantsova, Ludmila I.,Petrosyan, Valery S.

experimental part, p. 430 - 440 (2011/07/29)

The aminomethylation of the derivatives of trivalent organophosphorus acids, containing PH and POSiMe3 fragments with various bis- and tris(alkoxymethyl)amines and bis(alkoxymethyl)amino acids, is proposed as a convenient method for the synthesis of new bis- and trisphosphorylated amines and amino acids as well as their derivatives with four and five coordinated phosphorus. Also the three-components systems of phosphorous acid, paraformaldehyde, and amines are thoroughly investigated via the treatment of reaction mixtures with bis(trimethylsilyl)amine.

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