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CAS RN: 108-22-5 | Product Number: A0035

Isopropenyl Acetate


Purity: >98.0%(GC)
Synonyms:
  • Acetic Acid Isopropenyl Ester
Product Documents:
25ML
€16.00
3   ≥100 
500ML
€34.00
9   ≥40 

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Product Number A0035
Purity / Analysis Method >98.0%(GC)
Molecular Formula / Molecular Weight C__5H__8O__2 = 100.12 
Physical State (20 deg.C) Liquid
Storage Temperature Room Temperature (Recommended in a cool and dark place, <15°C)
CAS RN 108-22-5
Reaxys Registry Number 1280347
PubChem Substance ID 87561738
SDBS (AIST Spectral DB) 1423
Merck Index (14) 5203
MDL Number

MFCD00008709

Specifications
Appearance Colorless to Almost colorless clear liquid
Purity(GC) min. 98.0 %
Properties (reference)
Melting Point -93 °C
Boiling Point 97 °C
Flash point 16 °C
Specific Gravity (20/20) 0.92
Refractive Index 1.40
Solubility (miscible with) Benzene, Ether
GHS
Pictogram Pictogram Pictogram
Signal Word Danger
Hazard Statements H319 : Causes serious eye irritation.
H225 : Highly flammable liquid and vapour.
Precautionary Statements P210 : Keep away from heat, hot surfaces, sparks, open flames and other ignition sources. No smoking.
P233 : Keep container tightly closed.
P280 : Wear protective gloves/ protective clothing/ eye protection/ face protection.
P370 + P378 : In case of fire: Use dry sand, dry chemical or alcohol-resistant foam to extinguish.
P337 + P313 : If eye irritation persists: Get medical advice/ attention.
P303 + P361 + P353 : IF ON SKIN (or hair): Take off immediately all contaminated clothing. Rinse skin with water.
Related Laws:
EC Number 203-562-7
RTECS# UD4200000
Transport Information:
UN Number UN2403
Class 3
Packing Group II
HS Number 2915390090
Application
Acetylcholine Chloride: A Neurotransmitter in the Central and Peripheral Nervous Systems

A0035

References


Application
Synthesis of 4-Hydroxyquinazolines Using Gold’s Reagent

References

  • 1)Total Synthesis of the Proposed Structure of Briarellin J
  • 2)Protection for the Hydroxyl Group, Including 1,2- and 1,3-Diols
    • P. G. M. Wuts, in Greene’s Protective Groups in Organic Synthesis, 5th ed., ed. by P. G. M. Wuts, John Wiley & Sons, Inc., Hoboken, New Jersey, 2014, Chap. 2, 17.


PubMed Literature


Product Documents (Note: Some products will not have analytical charts available.)
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