3-Methyl-3-oxetanemethanol

Names

[ Name ]:
3-Methyl-3-oxetanemethanol

[Synonym ]:
3-Methyl-3-oxethanemethanol
MFCD00010273
(3-Methyl-oxetan-3-yl)-methanol
3-methyl-3-(hydroxy-methyl)-oxetane
3-Hydroxymethyl-3-Methyloxetane
3-Methyl-3-oxetanemethanol
3-methyl-3-oxetanyl-methyl alcohol
2-(Hydroxymethyl)-2-methyl-1,3-epoxypropane
(3-Methyl-3-oxetanyl)methanol
3-Oxetanemethanol, 3-methyl-
(3-methyloxetan-3-yl)methan-1-ol
(3-methyloxetan-3-yl)methanol
3-(Hydroxymethyl)-3-methyloxetane

Chemical & Physical Properties

[ Density]:
1.0±0.1 g/cm3

[ Boiling Point ]:
152.2±0.0 °C at 760 mmHg

[ Molecular Formula ]:
C₅H₁₀O₂

[ Molecular Weight ]:
102.132

[ Flash Point ]:
98.9±0.0 °C

[ Exact Mass ]:
102.068077

[ PSA ]:
29.46000

[ LogP ]:
-0.61

[ Vapour Pressure ]:
1.3±0.6 mmHg at 25°C

[ Index of Refraction ]:
1.444

[ Storage condition ]:
2-8°C

MSDS

Click to get detail MSDS

Safety Information

[ Symbol ]:

GHS07

[ Signal Word ]:
Warning

[ Hazard Statements ]:
H302-H317

[ Precautionary Statements ]:
P280

[ Personal Protective Equipment ]:
Eyeshields;Faceshields;full-face respirator (US);Gloves;multi-purpose combination respirator cartridge (US);type ABEK (EN14387) respirator filter

[ Hazard Codes ]:
Xi: Irritant;

[ Risk Phrases ]:
R43

[ Safety Phrases ]:
S23-S24/25-S36/37

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3

[ HS Code ]:
2932999099

Customs

[ HS Code ]: 2932999099

[ Summary ]:
2932999099. other heterocyclic compounds with oxygen hetero-atom(s) only. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%

Articles

Short stereoselective synthesis of alpha-substituted gamma-lactams.

J. Org. Chem. 71 , 2151, (2006)

A concise, stereoselective synthesis of alpha-substituted gamma-lactams is reported. gamma-Lactam scaffolds 2 and 3, possessing an Evans' chiral auxiliary and two types of N substituents, were success...

Synthesis of a Star-Shaped Copolymer with a Hyperbranched Poly (3-methyl-3-oxetanemethanol) Core and Tetrahydrofuran Arms by One-Pot Copolymerization. Hou J and Yan D.

Macromol. Rapid Commun. 23(8) , 456-59, (2002)

Functional poly (e-caprolactone) s via copolymerization of e-caprolactone and pyridyl disulfide-containing cyclic carbonate: controlled synthesis and facile access to reduction-sensitive biodegradable graft copolymer micelles. Chen W, et al.

Macromolecules 46(3) , 699-707, (2013)