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CAS

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868-16-6

Lithium bitartrate, a chemical compound and a salt of lithium and tartaric acid, is widely recognized for its mood-stabilizing properties. It functions by influencing neurotransmitter levels in the brain, which aids in mood stabilization and the mitigation of mood swings' severity and frequency.

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  • 868-16-6 Structure

  • Basic information

    1. Product Name: LITHIUM BITARTRATE
    2. Synonyms: LITHIUM HYDROGEN TARTRATE;LITHIUM BITARTRATE;(2R,3R)-2,3-Dihydroxybutanedioic acid hydrogen 1-lithium salt
    3. CAS NO:868-16-6
    4. Molecular Formula: C4H4O6*2Li
    5. Molecular Weight: 161.95
    6. EINECS: 212-771-2
    7. Product Categories: N/A
    8. Mol File: 868-16-6.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 399.3°C at 760 mmHg
    3. Flash Point: 209.4°C
    4. Appearance: /
    5. Density: N/A
    6. Vapor Pressure: 4.93E-08mmHg at 25°C
    7. Refractive Index: N/A
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: LITHIUM BITARTRATE(CAS DataBase Reference)
    11. NIST Chemistry Reference: LITHIUM BITARTRATE(868-16-6)
    12. EPA Substance Registry System: LITHIUM BITARTRATE(868-16-6)

  • 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: 868-16-6(Hazardous Substances Data)

868-16-6 Usage

Uses

Used in Pharmaceutical Industry:
Lithium bitartrate is utilized as a mood-stabilizing medication for the treatment of bipolar disorder. It is instrumental in managing the symptoms and preventing the recurrence of manic and depressive episodes.
Used in Food and Beverage Industry:
Lithium bitartrate serves as a stabilizer and buffering agent in certain food and beverage products. It contributes to maintaining the quality and consistency of these products, ensuring a stable shelf life and consumer experience.

Check Digit Verification of cas no

The CAS Registry Mumber 868-16-6 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 6 respectively.
Calculate Digit Verification of CAS Registry Number 868-16:
(5*8)+(4*6)+(3*8)+(2*1)+(1*6)=96
96 % 10 = 6
So 868-16-6 is a valid CAS Registry Number.
InChI:InChI=1/C4H6O6.Li/c5-1(3(7)8)2(6)4(9)10;/h1-2,5-6H,(H,7,8)(H,9,10);/q;+1/p-1/t1-,2-;/m1./s1

868-16-6SDS

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 lithium,2,3,4-trihydroxy-4-oxobutanoate

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:868-16-6 SDS

868-16-6Upstream product

868-16-6Downstream Products

868-16-6Relevant 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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