Paraldehyde

• Catalog No.: 76260
• CAS Number: 123-63-7
• M. F.: C6H12O3
• M. W.: 132.15768
• Purity: ≥97.0% (GC)

SYNONYMS

• Title: 三聚乙醛
• IUPAC name: 2,4,6-trimethyl-1,3,5-trioxane
• IUPAC Traditional name: paral
• Synonyms: 三聚醋醛; Paracetaldehyde; 2,4,6-Trimethyl-1,3,5-trioxacyclohexane; Acetaldehyde trimer; s-Trimethyltrioxymethylene; NSC 9799; 仲醛

DATABASE IDS

• CAS Number: 123-63-7
• Beilstein Number: 80142
• PubChem SID: 24886966
• MDL Number: MFCD00036208
• EC Number: 204-639-8

PROPERTIES

• Empirical Formula (Hill Notation): C6H12O3
• Purity: ≥97.0% (GC)
• Boiling Point: 123-124 °C
• Density: 0.994 g/mL at 20 °C(lit.)
• Flash Point: 24 °C
• Flash Point: 75.2 °F
• Refractive Index: n20/D 1.405
• Drug Control: USDEA Schedule IV
• GHS Signal Word: Warning
• GHS Hazard statements: H226
• Personal Protective Equipment: Eyeshields, Faceshields, full-face respirator (US), Gloves, multi-purpose combination respirator cartridge (US), type ABEK (EN14387) respirator filter
• RID/ADR: UN 1264 3/PG 3
• Risk Statements: 10
• RTECS: YK0525000
• Safety Statements: 29
• Hazard Class: 3
• UN Number: 1264
• Packing Group: 3
• German water hazard class: 1

DETAILS

Description (English)

Other Notes
Sales restrictions may apply
Application
Reactant involved in:
• Modified Sanford reaction1
• Synthesis of N-arylbenzoquinaldinium derivatives with antimicrobial activity2
• Hydroformylation of alkenylamines3
• Studies of molecules with inhibitory activity against HIV-1 integrase4
• Irregular Wittig reactions for the formation of α-hydroxyketones5

Description (简体中文)

Other Notes
可能实行销售限制
Application
Reactant involved in:
• Modified Sanford reaction1
• Synthesis of N-arylbenzoquinaldinium derivatives with antimicrobial activity2
• Hydroformylation of alkenylamines3
• Studies of molecules with inhibitory activity against HIV-1 integrase4
• Irregular Wittig reactions for the formation of α-hydroxyketones5