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16333-96-3

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16333-96-3 Usage

Uses

Acetyl phosphate is used in the study of pyruvate cleavage and formation in bacterium.

Check Digit Verification of cas no

The CAS Registry Mumber 16333-96-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,3,3 and 3 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 16333-96:
(7*1)+(6*6)+(5*3)+(4*3)+(3*3)+(2*9)+(1*6)=103
103 % 10 = 3
So 16333-96-3 is a valid CAS Registry Number.

16333-96-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name dilithium acetyl phosphate

1.2 Other means of identification

Product number -
Other names Dilithium acetylphosphate

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:16333-96-3 SDS

16333-96-3Downstream Products

16333-96-3Relevant articles and documents

Investigation of Lithium Acetyl Phosphate Synthesis Using Process Analytical Technology

Smith, Joseph P.,Obligacion, Jennifer V.,Dance, Zachary E. X.,Lomont, Justin P.,Ralbovsky, Nicole M.,Bu, Xiaodong,Mann, Benjamin F.

, p. 1402 - 1413 (2021/07/01)

Acetyl phosphate salts are common phosphate donors for enzymatic phosphorylation with kinases and are used in a variety of industrial biocatalytic processes. Due to their ever-increasing demand, synthesis of high-quality acetyl phosphate salts is critical for pharmaceutical process development, especially given that common impurities such as acetic acid and phosphate can inhibit the intended reaction. Current offline analytical methodologies for investigating the acetyl phosphate reagent quality are limited due to the hydrolytically unstable nature of the chemical species, resulting in its potential degradation before complete analysis may occur. It is therefore advantageous to synthesize high-purity acetyl phosphate using process analytical technology (PAT) tools to monitor reaction progress in real time. In this work, several PAT tools were employed specifically for the investigation of lithium acetyl phosphate synthesis, including in situ Fourier transform infrared spectroscopy, pH and temperature sensing, online optical microscopy, and focused beam reflectance measurements. These PAT tools offer a significant benefit by providing insights into reaction optimization, through observing the timing of temperature and pH changes, realizing a particle size target, and directly monitoring the consumption of reagents and formation of products. Results indicate that these online in situ methods are successful in detailed reaction monitoring and process characterization for the production of quality lithium acetyl phosphate, allowing for real-time reaction understanding.

Association Phenomena. 7. Mixed Chelate and Comicellar Catalysis of Acetyl Phosphate ''Olysis'' Reactions

Gutsche, C. David,Mei, George C.

, p. 7964 - 7967 (2007/10/02)

The decomposition of acetyl phosphate has been studied under conditions designed to catalyze the process via a combination of mixed chelate and comicelle formation.In the presence of n-dodecylamine under micelle-forming conditions, the rate of decomposition is increased by a factor of 275, the optimum pH for the catalysis being 8.5.In the presence of the polyamide 1-undecyl-N,N'-bisethylenediamine (7) and the metal ions Zn2+, Cu2+, and Ni2+, the rate of decomposition is increased by factors of 60-140 at pH 11.5 where compound 7 exists in the hydroxamate form.The kinetics of the latter process have been measured and found to be first-order throughout the reaction, indicating that compound 7 acts as a catalyst for the overall process of hydrolysis.The inclusion of n-hexanol or n-octylamine in the system, in the hope that comicellization would induce transfer of the acetyl group from the phosphate to the alcohol or amine, failed to yield positive results.

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