22007-56-3

Basic information

• Product Name: 1,2-octanediyl diacetate
• Synonyms: 1,2-octanediyl diacetate;1,2-Octanediol diacetate;Ai3-13061;Einecs 244-715-8
• CAS NO: 22007-56-3
• Molecular Formula: C₁₂H₂₂O₄
• Molecular Weight: 230.30068
• EINECS: 244-715-8
• Mol File: 22007-56-3.mol
• Article Data: 22

Chemical Properties

• Boiling Point: 286.1°Cat760mmHg
• Flash Point: 130.7°C
• Appearance: /
• Density: 0.984g/cm³
• Vapor Pressure: 0.0027mmHg at 25°C
• Refractive Index: 1.435
• CAS DataBase Reference: 1,2-octanediyl diacetate(CAS DataBase Reference)
• NIST Chemistry Reference: 1,2-octanediyl diacetate(22007-56-3)
• EPA Substance Registry System: 1,2-octanediyl diacetate(22007-56-3)

Safety Data

• Hazardous Substances Data: 22007-56-3(Hazardous Substances Data)

Usage

Physical state

Clear, colorless liquid

Odor

Mild, sweet

Solubility

Soluble in most organic solvents

Uses

1. Solvent in various consumer products
2. Fragrance ingredient in perfumes, colognes, and personal care products
3. Plasticizer in the production of polyvinyl chloride (PVC) and other polymers

Toxicity

Low toxicity, generally regarded as safe for use in applications

Potential health effects

May cause irritation to the skin, eyes, and respiratory system in high concentrations or with prolonged exposure

Industrial and commercial applications

Wide range of uses in various industries and commercial products

InChI:InChI=1/C12H22O4/c1-4-5-6-7-8-12(16-11(3)14)9-15-10(2)13/h12H,4-9H2,1-3H3

Upstream product

• 111-66-0 oct-1-ene 
• 546-67-8 lead(IV) tetraacetate 
• 1117-86-8 1,2-octandiol 
• 108-24-7 acetic anhydride 
• 64-19-7 acetic acid 
• 629-05-0 n-octyne 
• 136918-14-4 phthalimide 
• 3240-34-4 [bis(acetoxy)iodo]benzene 
• 2984-50-1 1,2-Epoxyoctane 
• 79-21-0 peracetic acid 

Relevant articles and documents

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Vicinal Difunctionalization of Alkenes under Iodine(III) Catalysis involving Lewis Base Adducts

The influence of a 2-pyridinyl substituent on the catalytic performance of aryl iodides as catalyst in iodine(III) chemistry was explored. An efficient Lewis base adduct between the pyridine nitrogen and the electrophilic iodine(III) center was identified and confirmed by X-ray analysis. This arrangement was shown to generate a kinetically competent superior catalyst structure for the catalytic dioxygenation of alkenes. It introduces the concept of Lewis base adduct formation as a kinetic factor in iodine(I/III) catalysis. (Figure presented.).

Aerobic Acetoxyhydroxylation of Alkenes Co-catalyzed by Organic Nitrite and Palladium

An aerobic acetoxyhydroxylation of alkenes cooperatively catalyzed by organic nitrite and palladium at room temperature using clean and cheap air as the sole oxidant has been developed. Various vicinal diols, diacetoxyalkanes, and dihalogenoalkanes have been synthesized. The gram-scale synthesis has also been approached. Vicinal difluorination and dichlorolation products have also been achieved via this reaction.