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Acetal
[CAS# 105-57-7]

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Identification
Classification Organic raw materials >> Aldehyde
Name Acetal
Synonyms 1,1-Diethoxyacetal; 1,1-Diethoxyethane; Acetaldehyde diethyl acetal
Molecular Structure CAS # 105-57-7, Acetal, 1,1-Diethoxyacetal, 1,1-Diethoxyethane, Acetaldehyde diethyl acetal
Molecular Formula C6H14O2
Molecular Weight 118.17
CAS Registry Number 105-57-7
EC Number 203-310-6
FEMA 2002
SMILES CCOC(C)OCC
Properties
Density 0.825
Melting point -100 ºC
Boiling point 103 ºC
Refractive index 1.379-1.385
Flash point -21 ºC
Water solubility 46 g/L (25 ºC)
Safety Data
Hazard Symbols symbol symbol   GHS02;GHS07 Danger    Details
Hazard Statements H225-H315-H319    Details
Precautionary Statements P210-P233-P240-P241-P242-P243-P264-P264+P265-P280-P302+P352-P303+P361+P353-P305+P351+P338-P321-P332+P317-P337+P317-P362+P364-P370+P378-P403+P235-P501    Details
Hazard Classification
up    Details
HazardClassCategory CodeHazard Statement
Skin irritationSkin Irrit.2H315
Flammable liquidsFlam. Liq.2H225
Eye irritationEye Irrit.2H319
Skin sensitizationSkin Sens.1H317
Flammable liquidsFlam. Liq.1H224
Skin corrosionSkin Corr.1H314
Serious eye damageEye Dam.1H318
Transport Information UN 1088
SDS Available
up Discovory and Applicatios
Acetal, an organic compound type characterized by the general formula R₂C(OR')₂, is central in organic chemistry and industrial applications. Acetals were first studied in the 19th century as chemists began investigating compounds capable of protecting functional groups in complex synthesis processes. The term "acetal" commonly refers to any compound where two alkoxy groups are bonded to a single carbon atom, stemming from initial studies on acetaldehyde derivatives. The reactivity and stability of acetal linkages in both synthetic and biological systems have established acetals as valuable compounds in multiple fields.

Structurally, acetals contain a carbon atom connected to two ether (–OR) groups and one or two alkyl (R) or aryl (Ar) groups. This configuration makes acetals highly stable under neutral or basic conditions, although they readily decompose in acidic environments. Acetals can be synthesized through the acid-catalyzed reaction of an aldehyde or ketone with an alcohol, forming a hemiacetal intermediate, which subsequently reacts with another alcohol molecule to yield the final acetal structure. This reactivity has made acetals valuable as protective groups in organic synthesis, shielding sensitive carbonyl groups during multi-step reactions.

In industrial and commercial contexts, acetals play critical roles in materials and manufacturing. Polyoxymethylene (POM), also known as acetal resin, is a widely used thermoplastic derived from formaldehyde, with applications spanning automotive components, consumer electronics, and precision parts. Due to its high strength, low friction, and excellent chemical resistance, acetal resin is used in manufacturing gears, fasteners, and bearing surfaces. In food packaging and medical devices, acetals are valued for their stability and low moisture absorption, which ensure the longevity and safety of end products.

Beyond manufacturing, acetals also serve in perfumery and pharmaceuticals, where they are synthesized to encapsulate and release fragrances and medicinal compounds gradually. Acetals derived from natural or synthetic aldehydes and alcohols are also used as flavoring agents due to their stability and pleasant aromas, contributing to the sensory qualities of food and beverages. Their stability and relatively low toxicity make them suitable for various consumer products, though regulatory standards govern their use, particularly in consumables.

The discovery and utilization of acetals have made a lasting impact across chemistry and industry. Their protective qualities in synthetic chemistry, resilience in materials, and contribution to consumer products reflect the versatility and ongoing relevance of acetal compounds in modern applications.
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