5299-61-6

Basic information

• Product Name: 6-Hydroxycaproic acid sodium salt
• Synonyms: 6-Hydroxycaproic acid sodium salt;6-Hydroxyhexanoic acid sodium salt
• CAS NO: 5299-61-6
• Molecular Formula: C₆H₁₁O₃*Na
• Molecular Weight: 0
• Mol File: 5299-61-6.mol
• Article Data: 10

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 6-Hydroxycaproic acid sodium salt(CAS DataBase Reference)
• NIST Chemistry Reference: 6-Hydroxycaproic acid sodium salt(5299-61-6)
• EPA Substance Registry System: 6-Hydroxycaproic acid sodium salt(5299-61-6)

Safety Data

• Hazardous Substances Data: 5299-61-6(Hazardous Substances Data)

Usage

Uses

Sodium 6-Hydroxycaproate is an intermediate in the synthesis of Mono-5-carboxy-n-pentyl-phthalate (M525495), which is a metabolite of Dibutyl phthalate (DBP) (D429495), which is widely used in consumer products.

Upstream product

• 502-44-3 hexahydro-2H-oxepin-2-one 

Downstream Products

• 99590-03-1 Acetic acid 6-(4,5-dimethoxy-2-methyl-3,6-dioxo-cyclohexa-1,4-dienyl)-hexyl ester 
• 77712-34-6 2,3-dimethoxy-5-methyl-6-(6-hydroxyhexyl)-1,4-benzoquinone 
• 104966-91-8 Acetic acid 6-(2-hydroxy-3,4-dimethoxy-6-methyl-phenyl)-6-oxo-hexyl ester 
• 104966-99-6 Acetic acid 6-(2-hydroxy-3,4-dimethoxy-6-methyl-phenyl)-hexyl ester 
• 104966-95-2 6-Hydroxy-1-(2-hydroxy-3,4-dimethoxy-6-methyl-phenyl)-hexan-1-one 
• 77712-33-5 2-(6-Hydroxy-hexyl)-5,6-dimethoxy-3-methyl-phenol 
• 174280-85-4 6-(diphenoxyphosphoryloxy)hexanoic acid 
• 219752-73-5 (R)-2-tert-Butoxycarbonylamino-6-[((R)-3-{(S)-2-[6-(diphenoxy-phosphoryloxy)-hexanoylamino]-propionylamino}-3-methoxycarbonyl-propyl)-methoxy-phosphinoylmethyl]-heptanedioic acid dimethyl ester 
• 219752-77-9 2-[6-(diphenoxy-phosphoryloxy)-hexanoylamino]-propionic acid tert-butyl ester 
• 219752-72-4 N-(2-S-propanoic acid)-6-<(diphenoxyphosphinyl)oxy>hexanamide 

Relevant articles and documents

Mild and chemoselective lactone ring-opening with (TMS)ONa. Mechanistic studies and application to sweroside derivatives

Mild and chemoselective opening of lactones with sodium trimethylsilanolate in high yields and aprotic solvents is described. Kinetic studies demonstrate that the BAc2 mechanistic pathway is followed. Nucleophilic attack of silanolate onto the carbonyl of the lactone moiety is the rate-determining step. NaOH present as an impurity accelerates the reaction. The method was further applied to the base-sensitive and stable lactones derived from highly functionalized iridoid derivatives.

CARBOXYLATED PHOSPHATIDIC ACID ESTERS

Novel compounds of formula in which R1 and R2 are phospholipid fatty acid residues and A is an aliphatic and/or cycloaliphatic hydrocarbon chain optionally substituted by hydroxy and/or further carboxylic functions. The novel compounds are useful for making liposomes of enhanced stability and entrapping capacity.

Development and Evaluation of Antisera for Detection of the O,O-Diethyl Phosphorothionate and Phosphorothionothiolate Organophosphorus Pesticides by Immunoassay

An immunochemical approach for class detection of organophosphorus pesticides was investigated. Synthesis of O,O-diethyl phosphorothionate haptens and their use in the generation of polyclonal antisera are described. An indirect inhibition format ELISA co