Sodium bisulfate monohydrate

Base Information

• Chemical Name: Sodium bisulfate monohydrate
• CAS No.: 10034-88-5
• Molecular Formula: NaHSO4^.H2O
• Molecular Weight: 138.077
• Hs Code.: 28331900
• Mol file: 10034-88-5.mol

Synonyms:Sulfuricacid, monosodium salt, monohydrate (8CI,9CI);Sodium bisulfate hydrate;Sodium sulfate monohydrate;Sodium hydrogen sulfate hydrate (1:1:1);

Chemical Property of Sodium bisulfate monohydrate

Chemical Property:

• Appearance/Colour: white adhering crystals
• Vapor Pressure: 3.35E-05mmHg at 25°C
• Melting Point: 58 °C
• Boiling Point: 330 °C at 760 mmHg
• PSA: 95.04000
• Density: 2.103
• LogP: 0.02110
• Storage Temp.: 5-15°C
• Sensitive.: Moisture Sensitive
• Solubility.: 1080g/l
• Water Solubility.: 670 g/L

Purity/Quality:

99% ^*data from raw suppliers

Sodium bisulfate monohydrate ^*data from reagent suppliers

Safty Information:

• Pictogram(s): Xi
• Hazard Codes: Xi,C
• Statements: 41-34
• Safety Statements: 24-26-45-36/37/39-27-22

MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:

• Description: Sodium bisulfate monohydrate is an organic compound with chemical formula H3NaO5S. The compound has a characteristic odor and is moderately soluble in water.
• Uses: Sodium bisulfate monohydrate is acid soluble and is used as a source of sodium for uses compatible with sulfates. Sulfate compounds are esters or salts of sulfuric acid that are formed by replacing one or both hydrogens with metal. Since most metal sulfate compounds are soluble in water, they are normally used in water treatment. Sodium bisulfate monohydrate (Sodium hydrogen sulfate monohydrate) may be employed as a catalyst in the following studies:Synthesis of n-butyl acetate.Esterification reaction of primary and secondary alcohols with aliphatic carboxylic acids.Synthesis of iso-amyl acetate.Synthesis of herbicide, 2,4-D butylate(butyl 2,4-dichlorophenoxyacetate).

Technology Process of Sodium bisulfate monohydrate

There total 5 articles about Sodium bisulfate monohydrate 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:

sulfuric acid (7664-93-9) + water (7732-18-5) + sodium chloride (7647-14-5) → hydrogenchloride (7647-01-0,15364-23-5) + sodium hydrogensulfate monohydrate (10034-88-5)

Guidance literature:

In water; exposure of powdered NaCl to H2SO4 soln. with compn. of NaCl:H2O:H2SO4 of 2:20:1 at 85% rel. humidities; not isolated, detn. by Raman spectroscopy; Kinetics;

DOI:10.1021/ja001469x

Reference yield:

sulfuric acid (7664-93-9) + water (7732-18-5) + sodium chloride (7647-14-5) → sodium hydrogensulfate monohydrate (10034-88-5) + Na hydrogensulfate (7681-38-1)

Guidance literature:

In water; exposure of powdered NaCl to H2SO4 soln. with compn. of NaCl:H2O:H2SO4 of 2:8:1 for 24 h at 85% rel. humidities; not isolated, detn. by Raman spectroscopy; Kinetics;

DOI:10.1021/ja001469x

Reference yield:

sulfuric acid (7664-93-9) + water (7732-18-5) + sodium chloride (7647-14-5) → sodium hydrogensulfate monohydrate (10034-88-5)

Guidance literature:

In sulfuric acid; exposure of NaCl with 96 wt% H2SO4 (0.5:1 H2SO4:NaCl) in dry bag; storage in desiccator for several days; exposure to environment of 100% rel. humidities for 40 min; not isolated, detn. by Raman spectroscopy; Kinetics;

DOI:10.1021/ja001469x

upstream raw materials:

sulfuric acid

water

sodium chloride

sodium sulfate

Downstream raw materials:

1-acetyl-4-aminomethylpiperidine

2-isopropyl-5,5-bis(carboethoxy)-1,3-dioxane

(+/-)-ethyl 4-methyl-3-phenylpentanoate

[Pd(SO₄)(1,3-bis(diphenylphosphino)propane)]

Refernces