Toluene diisocyanate manufacturer Knowledge m-nitrobenzenesulfonic acid sodium salt m-nitrobenzenesulfonic acid sodium salt

m-nitrobenzenesulfonic acid sodium salt m-nitrobenzenesulfonic acid sodium salt

Structural formula of m-nitrobenzene sulfonate sodium salt

Structural formula

Business number 03L3
Molecular formula C6H4NNaO5S
Molecular weight 225.16
label

3-Sodium nitrobenzene sulfonate,

Sodium m-nitrobenzene sulfonate,

M-Sodium nitrobenzene sulfonate,

3-Nitrobenzenesulfonic acid sodium salt,

Sodium 3-nitrobenzenesulfonate,

chemical additives,

anionic surfactant

Numbering system

CAS number:127-68-4

MDL number:MFCD00007490

EINECS number:204-857-3

RTECS number:DB7195000

BRN number:3639982

PubChem number:24853484

Physical property data

1. Properties: white to yellow crystals or uniform powder

2. Melting point (℃): 70

3. Water solubility: soluble in water, ethanol, ether and acetone , and gradually decompose in aqueous solution.

Toxicological data

1. Skin/eye irritation: Rabbit skin standard Drez eye dye test: 500mg/24H has a slight irritating effect on the skin.

Standard Drez eye dyeing test on rabbit eyes: 20mg/24H has a moderate irritating effect on the eyes.

2. Acute toxicity: Rat oral LD50: 11000mg/kg

Ecological data

None

Molecular structure data

None

Compute chemical data

1. Reference value for hydrophobic parameter calculation (XlogP): None

2. Number of hydrogen bond donors: 0

3. Number of hydrogen bond acceptors: 5

4. Number of rotatable chemical bonds: 0

5. Number of tautomers: none

6. Topological molecule polar surface area 111

7. Number of heavy atoms: 14

8. Surface charge: 0

9. Complexity: 274

10. Number of isotope atoms: 0

11. Determine the number of atomic stereocenters: 0

12. Uncertain number of atomic stereocenters: 0

13. Determine the number of chemical bond stereocenters: 0

14. Number of uncertain chemical bond stereocenters: 0

15. Number of covalent bond units: 2

Properties and stability

Acid, alkali and hard water resistant. It has oxidizing properties in neutral and alkaline media, which can offset the reducing power of insurance powder and carving powder.

Storage method

Production equipment should be sealed, and operators should wear protective equipment to prevent accidental ingestion.

Packaged in chemical fiber drums lined with plastic bags, stored in a cool, ventilated and dry place, with a storage period of two years. Store and transport according to drug regulations.

Synthesis method

1. Nitrobenzene sulfonation method: Industrial production can be obtained by nitrobenzene sulfonation and neutralization. Raw material consumption quota: benzene (98%) 400kg/t; sulfuric acid (98%) 550kg/t; nitric acid (98%) 390kg/t; liquid alkali (30%) 500kg/t; fuming sulfuric acid (containing SO320%) 410kg /t; lime milk 550kg/t; soda ash (95%) 30kg/t.

2. Benzene sulfonation method Benzene is sulfonated with sulfuric acid, and then nitrated with nitric acid to produce m-nitrobenzene sulfonic acid, which is then neutralized with milk of lime and replaced with sodium carbonate or sodium hydroxide to obtain the finished product.

Purpose

1. Used as vat dyes; anti-staining agent for sulfur dyes and color-forming protective agents for dyes, ship rust removers and electroplating nickel removers. It is also an intermediate between dyes and vanillin. It can also be used as a chemical reagent in chemical analysis.

2. This product is a mild oxidizing agent, used as a dyeing auxiliary. It can protect the color light when fabric printing or pad dyeing is steamed; it can prevent knife wires and cover sizing when fabrics are scouring and mercerizing; it can offset the effects of reducing substances during printing and dyeing. It can also be used as an oxidizing agent in dye synthesis. It is also an intermediate for synthetic dyes, a rust remover in the shipbuilding industry and a nickel remover in the electric power industry.

This article is from the Internet, does not represent the position of Toluene diisocyanate reproduced please specify the source.https://www.chemicalchem.com/archives/26794

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