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868-17-7

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868-17-7 Usage

Description

Lithium tartrate is a lithium salt compound that is formed from the combination of lithium and tartaric acid. It is recognized for its role in pharmaceuticals and research, where it serves as a source of lithium for medication and as a reagent in chemical synthesis and analysis. Its potential effects on mood stabilization in bipolar disorder have been studied, and it has been utilized in the treatment of certain psychiatric and neurological conditions. Furthermore, lithium tartrate has been investigated for its possible applications in treating specific types of cancer and neurodegenerative disorders. However, it is crucial to handle lithium tartrate with care due to its significant toxic effects if not used properly and under medical supervision.

Uses

Used in Pharmaceutical Industry:
Lithium tartrate is used as a mood stabilizer for the treatment of bipolar disorder, helping to manage the extreme mood swings associated with the condition.
Used in Research and Chemical Synthesis:
Lithium tartrate is used as a reagent in chemical synthesis and analysis, contributing to the development of new compounds and understanding of chemical reactions.
Used in Treatment of Psychiatric and Neurological Conditions:
Lithium tartrate is used as a therapeutic agent in the management of certain psychiatric and neurological conditions, leveraging its mood-stabilizing properties.
Used in Cancer and Neurodegenerative Disorder Research:
Lithium tartrate is used in research for its potential applications in the treatment of specific types of cancer and neurodegenerative disorders, exploring its effects on disease progression and management.

Check Digit Verification of cas no

The CAS Registry Mumber 868-17-7 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 8,6 and 8 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 868-17:
(5*8)+(4*6)+(3*8)+(2*1)+(1*7)=97
97 % 10 = 7
So 868-17-7 is a valid CAS Registry Number.
InChI:InChI=1/C4H6O6.2Li/c5-1(3(7)8)2(6)4(9)10;;/h1-2,5-6H,(H,7,8)(H,9,10);;/q;2*+1/p-2

868-17-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name Dilithium tartarate

1.2 Other means of identification

Product number -
Other names Butanedioic acid,2,3-dihydroxy-(2R,3R)-,lithium salt (1:1)

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:868-17-7 SDS

868-17-7Upstream product

868-17-7Downstream Products

868-17-7Relevant articles and documents

Phase selection during the crystallization of metal-organic frameworks; Thermodynamic and kinetic factors in the lithium tartrate system

Yeung, Hamish Hei-Man,Cheetham, Anthony Kevin

supporting information, p. 95 - 102 (2014/01/06)

We report the phase behaviour of chiral, racemic and meso-lithium tartrate frameworks, which was examined as a function of solvent system, temperature and ligand isomer. Through our comprehensive investigation of this system of 14 diverse phases, we have gained detailed insight into the effect of synthesis conditions on product structure, and elucidated the thermodynamic and kinetic factors involved in phase selection. Reactions in ethanol between lithium acetate and chiral, racemic and meso-tartaric acids give rise to anhydrous kinetic products; polymorphs with higher entropy tend to appear at high temperatures. Reactions at room temperature in water-ethanol mixtures give rise to hydrated kinetic products, including two new crystal structures, [Li 2(d,l-tartrate)(H2O)2]n in P1 and [Li2(meso-tartrate)(H2O)0.5]n in C2221, whose structures are contrasted with known anhydrous products. Reactions at elevated temperatures in water-ethanol mixtures result in the formation of low enthalpy, anhydrous products and, furthermore, the global minimum energy structure appears at high temperatures in all cases owing to in situ ligand isomerization.

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