SODIUM BITARTRATE

Base Information

• Chemical Name: SODIUM BITARTRATE
• CAS No.: 526-94-3
• Molecular Formula: C4H6 O6 . Na
• Molecular Weight: 172.07
• Hs Code.: 29181990
• Mol file: 526-94-3.mol

Synonyms:Butanedioicacid, 2,3-dihydroxy- (2R,3R)-, monosodium salt (9CI);Butanedioic acid,2,3-dihydroxy-[R-(R*,R*)]-, monosodium salt;Tartaric acid, monosodium salt(8CI);Monobasic sodium tartrate;Monosodium L-(+)-tartrate;Monosodiumtartrate;Sodium acid tartrate;Sodium bitartrate;Sodium hydrogen tartrate;

Chemical Property of SODIUM BITARTRATE

Chemical Property:

• Appearance/Colour: white crystalline powder
• Melting Point: 253 °C (dec.)(lit.)
• Boiling Point: 399.3°Cat760mmHg
• Flash Point: 209.4°C
• PSA: 117.89000
• Density: g/cm³
• LogP: -3.45730
• Solubility.: H2O: 0.1 M at 20 °C, clear, colorless
• Water Solubility.: Soluble in water.

Purity/Quality:

98%,99%, ^*data from raw suppliers

Sodium hydrogen tartrate ^*data from reagent suppliers

Safty Information:

• Safety Statements: 22-24/25

MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:

• Description: Mono sodium tartrate or sodium bitartrate is a sodium salt of tartaric acid. As a food additive it is used as an acidity regulator and is known by the E number E335.
• Uses: Analysis (testing for potassium), effervescing mixture, nutrient media. Sodium hydrogen L-tartrate is used for detecting potassium and in nutrient media. It also used as a food additive and an acidity regulator. Sodium hydrogentartrate may also be used in the preparation of sodium citrate-sodium tartrate reagent, which can complex with interfering metals during the colorimetric estimation of ammonium ions in soil samples. The modification of supported nickel catalysts with sodium hydrogentartrate leads to enhanced enantiomeric excess (ee) during the hydrogenation of methyl acetoacetate.

Technology Process of SODIUM BITARTRATE

There total 28 articles about SODIUM BITARTRATE 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: 90.0%

L-Tartaric acid (87-69-4,138508-61-9) → sodium L-tartrate (526-94-3,868-18-8,4504-50-1,14475-11-7,21106-15-0,21348-52-7,21595-79-9,22476-77-3,25817-08-7,51307-92-7,60131-40-0,64183-71-7,109175-69-1)

Guidance literature:

With sodium hydroxide; In methanol; water;

DOI:10.1016/j.ica.2017.10.037

Reference yield:

C34H50O10 + diethyl (2R,3R)-tartrate (87-91-2) + 3,7,12-trioxo-5β-cholan-24-oic acid ethyl ester (52718-49-7) → C28H35O10(3-)*3Na(1+) + Biliton (145-41-5) + sodium L-tartrate (526-94-3,868-18-8,4504-50-1,14475-11-7,21106-15-0,21348-52-7,21595-79-9,22476-77-3,25817-08-7,51307-92-7,60131-40-0,64183-71-7,109175-69-1)

Guidance literature:

With methanol; sodium hydroxide; water;

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) + sodium L-tartrate (526-94-3,868-18-8,4504-50-1,14475-11-7,21106-15-0,21348-52-7,21595-79-9,22476-77-3,25817-08-7,51307-92-7,60131-40-0,64183-71-7,109175-69-1)

Guidance literature:

With sodium hydroxide; In water; toluene; Product distribution / selectivity;

upstream raw materials:

D-glucose

DL-tartaric acid

sodium hydroxide

sodium oxalate

Downstream raw materials:

sodium potassium racemate*4H₂O

potassium bitartrate

rochelle salt

sodium potassium racemate*3H₂O

Refernces

• 1、 Berijani, Kayhaneh,Hosseini-Monfared, Hassan. "Collaborative effect of Mn-porphyrin and mesoporous SBA-15 in the enantioselective epoxidation of olefins with oxygen". . p. 113 - 120. Retrieved 2017/11/10.
• 2、 Butch, Christopher,Cope, Elizabeth D.,Pollet, Pamela,Gelbaum, Leslie,Krishnamurthy, Ramanarayanan,Liotta, Charles L.. "Production of tartrates by cyanide-mediated dimerization of glyoxylate: A potential abiotic pathway to the citric acid cycle". supporting information. p. 13440 - 13445. Retrieved 2013/09/24.