Ammonium L-tartrate

Base Information

• Chemical Name: Ammonium L-tartrate
• CAS No.: 3164-29-2
• Molecular Formula: C4H12O6N2
• Molecular Weight: 184.149
• Hs Code.: 29181300
• Mol file: 3164-29-2.mol

Synonyms:Ammoniumtartrate ((NH4)2O6C4H4) (6CI,7CI);Butanedioic acid, 2,3-dihydroxy- (2R,3R)-,diammonium salt (9CI);Butanedioic acid, 2,3-dihydroxy- [R-(R*,R*)]-,diammonium salt;Tartaric acid, diammonium salt (8CI);Ammonium d-tartrate;Ammonium tartrate;Diammonium L-(+)-tartrate;Diammonium d-tartrate;Diammoniumtartrate;L-Tartaric acid ammonium salt;

Chemical Property of Ammonium L-tartrate

Chemical Property:

• Appearance/Colour: white crystalline powder
• Vapor Pressure: 1.26E-11mmHg at 25°C
• Melting Point: decomposes [CRC10]
• Refractive Index: 1.4800 (estimate)
• Boiling Point: 399.3 °C at 760 mmHg
• Flash Point: 209.4 °C
• PSA: 120.72000
• Density: 1.601 g/mL at 25 °C(lit.)
• LogP: -4.03960
• Storage Temp.: room temp
• Sensitive.: Hygroscopic
• Solubility.: H2O: 1 M at 20 °C, clear, colorless
• Water Solubility.: 63 g/L (15 ºC)

Purity/Quality:

99.9% ^*data from raw suppliers

Ammonium tartrate dibasic ^*data from reagent suppliers

Safty Information:

• Pictogram(s): Xn
• Hazard Codes: Xn
• Statements: 20/21/22-36/37/38
• Safety Statements: 24/25-36-26

MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:

• Uses: Textile industry, medicine. Ammonium L-(+)-tartrate finds application in the textile and pharmaceutical industries. It is also used to study protein structural analysis, biochemicals and reagents, biological buffers, chelators and proteomics. It acts as a nitrogen source in biological applications and cell culture media. Further, it is used in the study of crystal optimization research and preliminary diffraction data analysis of the Smad1 MH1 domain bonded to a palindromic SBE DNA element.

Technology Process of Ammonium L-tartrate

There total 2 articles about Ammonium L-tartrate which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

(1R,2R)-2-hydroxy-1-(methylamino)-1,2,3,4-tetrahydronaphthalene L-(+)-tartrate salt → (+)-(1R,2R)-trans-1,2,3,4-tetrahydro-1-(methylamino)2-naphthalenol (169106-10-9) + diammonium tartate (3164-29-2)

Guidance literature:

With ammonium hydroxide; sodium chloride; In tert-butyl methyl ether; water; pH=> 8;

Reference yield:

(1S,4R)-4-aminocyclopent-2-ene-1-carboxylic acid methyl ester tartrate (419563-22-7) → (1S,4R)-(-)-methyl-4-aminocyclopent-2-en-1-carboxylate hydrochloride (138923-03-2,152279-17-9,352226-74-5,773006-65-8) + diammonium tartate (3164-29-2)

Guidance literature:

With ammonia; In methanol; water; at 20 ℃; for 1h; Product distribution / selectivity;

upstream raw materials:

(1S,4R)-4-aminocyclopent-2-ene-1-carboxylic acid methyl ester tartrate

Refernces

• 1、 -. "Process for synthesis of D1 receptor antagonists". Page/Page column 8. . Retrieved 2010/01/31.