ChemicalBook >> CAS DataBase List >>Pivalolactone.

Pivalolactone.

CAS No.
1955-45-9
Chemical Name:
Pivalolactone.
Synonyms
NCI-C04126;NCI-C-04126;Pivalolactone.;PPIVALOLACTONE;Dimethyl propiolactone;3,3-DIMETHYL-2-OXETANONE;2-Oxetanone, 3,3-dimethyl-;Pivalolactone (in chloroform ~1.6% w/v);2,2-Dimethyl-3-hydroxypropanoic acid lactone
CBNumber:
CB31251899
Molecular Formula:
C5H8O2
Molecular Weight:
100.12
MDL Number:
MFCD01709494
MOL File:
1955-45-9.mol
Last updated:2023-05-25 18:01:05

Pivalolactone. Properties

Melting point -12.9°C
Boiling point 51°C@20mmHg.
Density 0.9971 (rough estimate)
refractive index 1.4043 (estimate)
solubility soluble in Chloroform, Methanol
form Colourless Solution
Stability Stable. Combustible. Incompatible with strong oxidizing agents.
LogP -0.243 (est)
FDA UNII 6813U5R1GP
EPA Substance Registry System Pivalolactone (1955-45-9)

Pivalolactone. price

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
American Custom Chemicals Corporation CHM0158265 PIVALOLACTONE 95.00% 1955-45-9 100MG $739.2 2021-12-16 Buy
American Custom Chemicals Corporation CHM0158265 PIVALOLACTONE 95.00% 1955-45-9 3.125ML $836 2021-12-16 Buy
American Custom Chemicals Corporation CHM0158265 PIVALOLACTONE 95.00% 1955-45-9 1G $1871.1 2021-12-16 Buy
American Custom Chemicals Corporation CHM0158265 PIVALOLACTONE 95.00% 1955-45-9 31.25ML $1958 2021-12-16 Buy
Product number Packaging Price Buy
CHM0158265 100MG $739.2 Buy
CHM0158265 3.125ML $836 Buy
CHM0158265 1G $1871.1 Buy
CHM0158265 31.25ML $1958 Buy

Pivalolactone. Chemical Properties,Uses,Production

Chemical Properties

colourless liquid

Uses

Carcinogenic agent. Shows mutagenicity

Synthesis Reference(s)

Tetrahedron Letters, 10, p. 1047, 1969 DOI: 10.1017/S0009838800024678

General Description

Clear colorless liquid.

Air & Water Reactions

Pivalolactone. is unstable in water. Slowly hydrolyzes

Reactivity Profile

Pivalolactone. is an ester. Esters react with acids to liberate heat along with alcohols and acids. Strong oxidizing acids may cause a vigorous reaction that is sufficiently exothermic to ignite the reaction products. Heat is also generated by the interaction of esters with caustic solutions. Flammable hydrogen is generated by mixing esters with alkali metals and hydrides. Pivalolactone. is incompatible with alkanes.

Fire Hazard

Flash point data for Pivalolactone. are not available; however, Pivalolactone. is probably combustible.

Safety Profile

Poison by ingestion. Questionable carcinogen with experimental carcinogenic and tumorigenic data. Mutation data reported. When heated to decomposition it emits acrid smoke and irritating fumes.

Pivalolactone. Preparation Products And Raw materials

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NCI-C04126 NCI-C-04126 Pivalolactone. 3,3-DIMETHYL-2-OXETANONE PPIVALOLACTONE 2,2-Dimethyl-3-hydroxypropanoic acid lactone Dimethyl propiolactone Pivalolactone (in chloroform ~1.6% w/v) 2-Oxetanone, 3,3-dimethyl- 1955-45-9 Heterocycles