Home > Compound List > Product Information
Paraldehyde_Molecular_structure_CAS_123-63-7)
Click picture or here to close

Paraldehyde

Catalog No. 76260 Name Sigma Aldrich
CAS Number 123-63-7 Website http://www.sigmaaldrich.com
M. F. C6H12O3 Telephone 1-800-521-8956
M. W. 132.15768 Fax
Purity ≥97.0% (GC) Email
Storage Chembase ID: 123396

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 Pictograms GHS02
GHS Signal Word Warning
GHS Hazard statements H226
MSDS Link Download
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

REFERENCES