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LITHIUM LACTATE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

16891-53-5

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16891-53-5 Usage

Chemical Properties

White crystals

Check Digit Verification of cas no

The CAS Registry Mumber 16891-53-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,8,9 and 1 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 16891-53:
(7*1)+(6*6)+(5*8)+(4*9)+(3*1)+(2*5)+(1*3)=135
135 % 10 = 5
So 16891-53-5 is a valid CAS Registry Number.
InChI:InChI=1/C3H6O3.Na/c1-2(4)3(5)6;/h2,4H,1H3,(H,5,6);/q;+1/p-1/t2-;/m0./s1

16891-53-5SDS

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 LITHIUM LACTATE

1.2 Other means of identification

Product number -
Other names Monolithium phosphate

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:16891-53-5 SDS

16891-53-5Upstream product

16891-53-5Related news

LITHIUM LACTATE (cas 16891-53-5) as an ESR dosimeter08/02/2019

The feasibility of lithium lactate (Li-lactate: CH3CH(OH)COOLi) as an electron spin resonance (ESR) dosimeter material has been studied and compared with lactose and a conventional alanine dosimeter. The ESR spectra of Li-lactate and lactose with the spectroscopic splitting g-factors of 2.0029 ±...detailed

16891-53-5Relevant academic research and scientific papers

Complete conversion of l-lactate into d-lactate. A generic approach involving enzymatic catalysis, electrochemical oxidation of NADH, and electrochemical reduction of pyruvate

Biade, Azz-Eddine,Bourdillon, Christian,Laval, Jean-Marc,Mairesse, Gilles,Moiroux, Jacques

, p. 893 - 897 (2007/10/02)

L-Lactate was converted into D-lactate with a yield better than 97%, the system involving stereospecific catalysis of L-lactate oxidation by the rather cheap L-lactate dehydrogenase plus electrochemical regeneration of NAD+ at the anode and electrochemical reduction of pyruvate at the cathode. Such an approach can be extended to mere deracemization or complete inversion of all types of chiral α-alcohol-acids provided that the dehydrogenase related to the isomer to be inverted is available. Efficiency was not limited by enzyme or coenzyme deactivations.

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