95387-98-7

Basic information

• Product Name: ACRYLIC ACID (1-13C)
• Synonyms: ACRYLIC ACID (1-13C);ACRYLIC-1-13C ACID, 99 ATOM % 13C
• CAS NO: 95387-98-7
• Molecular Formula: C₃H₄O₂
• Molecular Weight: 73.07
• Product Categories: A;Alphabetical Listings;Stable Isotopes
• Mol File: 95387-98-7.mol
• Article Data: 3

Chemical Properties

• Melting Point: 13 °C(lit.)
• Boiling Point: 139 °C(lit.)
• Flash Point: 130 °F
• Appearance: /
• Density: 1.065 g/mL at 25 °C
• Refractive Index: n20/D 1.4202(lit.)
• CAS DataBase Reference: ACRYLIC ACID (1-13C)(CAS DataBase Reference)
• NIST Chemistry Reference: ACRYLIC ACID (1-13C)(95387-98-7)
• EPA Substance Registry System: ACRYLIC ACID (1-13C)(95387-98-7)

Safety Data

• Hazard Codes: C,N
• Statements: 10-34-50-35-20/21/22
• Safety Statements: 26-36-45-61-36/37/39
• RIDADR: UN 2218 8/PG 2
• WGK Germany: 3
• Hazardous Substances Data: 95387-98-7(Hazardous Substances Data)

Usage

InChI:InChI=1/C3H4O2/c1-2-3(4)5/h2H,1H2,(H,4,5)/i3+1

Upstream product

• 1111-72-4 carbon dioxide 
• 1826-67-1 vinyl magnesium bromide 
• 51956-33-3 [13C]barium carbonate 
• 1641-69-6 [13C]Carbon monoxide 

Relevant articles and documents

The Structure of Propadienone

A reanalysis of the vibrational ground-state microwave spectra of various isotopic versions of propadienone including lines assigned to the new 1-13C isotope, and taking into account the molecular nonrigidity, has been undertaken in order to determine more precisely the molecular structure.The nonlinear heavy-atom chain is found to have a zigzag conformation with angles C1C2C3=144.5 deg and OC1C2=169.4 deg.The vibrational potential function corresponding to this unusual structure has aspects that can be linked with structural features of a number of related molecules.

A MECHANISTIC STUDY OF PYRROLE FORMATION IN THE HBF4-CATALYZED THERMOLYSIS OF CYCLOPROPYL KETIMINES.

A study of the HBF4-catalyzed rearrangement of 1-(1-piperidino)cyclopropyl ketimines to 2-substituted pyrroles has been conducted using carbon-13 labeled starting material.The results support the formation of a bicyclic aziridine-containing intermediate.