13495-04-0

Basic information

• Product Name: HEPTALDEHYDE SODIUM BISULFITE
• Synonyms: HEPTALDEHYDE SODIUM BISULFITE;Heptanal Sodium Bisulfite
• CAS NO: 13495-04-0
• Molecular Formula: C₇H₁₅O₄S*Na
• Molecular Weight: 218.24637
• Mol File: 13495-04-0.mol
• Article Data: 3

Chemical Properties

• Appearance: /
• CAS DataBase Reference: HEPTALDEHYDE SODIUM BISULFITE(CAS DataBase Reference)
• NIST Chemistry Reference: HEPTALDEHYDE SODIUM BISULFITE(13495-04-0)
• EPA Substance Registry System: HEPTALDEHYDE SODIUM BISULFITE(13495-04-0)

Safety Data

• Hazardous Substances Data: 13495-04-0(Hazardous Substances Data)

Usage

Uses

In antifungal compositions.

InChI:InChI=1/C7H16O4S.Na/c1-2-3-4-5-6-7(8)12(9,10)11;/h7-8H,2-6H2,1H3,(H,9,10,11);/q;+1/p-1

Upstream product

• 111-70-6 n-heptan1ol 
• 111-71-7 heptanal 

Downstream Products

• 7664-93-9 sulfuric acid 
• 95513-28-3 (2S)-cis-1-(phenylsulfonyl)-2-(1-<(phenylsulfonyl)oxy>butyl)-5-heptylpyrrolidine 
• 95513-21-6 (2S)-cis-1-benzyl-5-heptylproline tert-butyl ester 
• 95513-23-8 (2S)-trans-1-benzyl-5-heptylproline tert-butyl ester 
• 95513-29-4 (2S)-cis-5-butyl-2-heptyl-1-(phenylsulfonyl)pyrrolidine 
• 95513-54-5 1-((2S,5S)-1-Benzyl-5-heptyl-pyrrolidin-2-yl)-butan-1-one 
• 95513-24-9 (2S)-cis-1-benzyl-5-heptylproline 
• 95513-25-0 (2S)-cis-1-benzyl-2-(1-hydroxybutyl)-5-heptylpyrrolidine 
• 95587-06-7 (2R,5S)-1-Benzyl-5-heptyl-pyrrolidine-2-carbonitrile 
• 95513-33-0 (2S,5S)-1-Benzyl-5-heptyl-pyrrolidine-2-carbonitrile 
• 95513-16-9 (2S)-1-benzyl-5-(1-<(benzyloxy)carbonyl>heptylidene)proline tert-butyl ester 
• 95513-14-7 benzyl 2-(<(trifluoromethyl)sulfonyl>oxy)octanoate 
• 95513-39-6 (5S)-1-benzyl-2-butyl-5-heptylproline tert-butyl ester 
• 95513-27-2 (2S)-cis-1-(phenylsulfonyl)-2-(1-hydroxybutyl)-5-heptylpyrrolidine 

Relevant articles and documents

A TEMPO-like nitroxide combined with an alkyl-substituted pyridine: An efficient catalytic system for the selective oxidation of alcohols with iodine

An efficient method for the oxidation of alcohols to aldehydes or ketones in a two-phase CH2Cl2/NaHCO3 (aq.) system, using iodine and catalytic amounts of 4-acetylamino-2,2,6,6-tetramethylpiperidine-1-oxyl and 2,4,6-trimethylpyridine, was developed. The performance of the method was demonstrated by the selective oxidation of 37 variously substituted alcohols in ≥90% yield, including the gram-scale synthesis of the important chemical 2,5-diformylfuran from biomass-derived 5-hydroxylmethylfurfural.

A NOVEL AND VERSATILE SEPARATION METHOD FOR ALDEHYDES

An aqueous solution of sodium ε-amino-n-caproate can be used for efficient and simple separation of aldehydes, overcoming the difficulties associated with the NaHSO3 method.Keywords - separation of aldehydes; Schiff base of amino acid; ω-amino acid; sodium ε-amino-n-caproate; sodium bisulfite adduct of aldehydes