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3-tert-Butoxy-3-oxopropanoic acid

Names

[ CAS No. ]:
40052-13-9

[ Name ]:
3-tert-Butoxy-3-oxopropanoic acid

[Synonym ]:
3-[(2-Methyl-2-propanyl)oxy]-3-oxopropanoic acid
mono-tert-Butyl malonate
3-[(2-methylpropan-2-yl)oxy]-3-oxopropanoic acid
Propanedioic acid, mono(1,1-dimethylethyl) ester
tert-Butyl Hydrogen Malonate
Malonic Acid Mono-tert-butyl Ester
MFCD00191886
3-tert-Butoxy-3-oxopropanoic acid
3-(tert-Butoxy)-3-oxopropanoic acid

Chemical & Physical Properties

[ Density]:
1.1±0.1 g/cm3

[ Boiling Point ]:
250.5±23.0 °C at 760 mmHg

[ Melting Point ]:
19-20 °C(lit.)

[ Molecular Formula ]:
C7H12O4

[ Molecular Weight ]:
160.168

[ Flash Point ]:
97.7±16.1 °C

[ Exact Mass ]:
160.073563

[ PSA ]:
63.60000

[ LogP ]:
1.04

[ Vapour Pressure ]:
0.0±1.1 mmHg at 25°C

[ Index of Refraction ]:
1.444

MSDS

Safety Information

[ Symbol ]:

GHS05, GHS06

[ Signal Word ]:
Danger

[ Hazard Statements ]:
H314-H330

[ Precautionary Statements ]:
P260-P280-P284-P305 + P351 + P338-P310

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

[ Hazard Codes ]:
T

[ Risk Phrases ]:
R26

[ Safety Phrases ]:
S26-S27-S36/37/39-S45

[ RIDADR ]:
UN 2922 8/PG 3

[ WGK Germany ]:
3

[ Hazard Class ]:
8.0, 6.1

[ HS Code ]:
2918990090

Precursor & DownStream

Customs

[ HS Code ]: 2918990090

[ Summary ]:
2918990090. other carboxylic acids with additional oxygen function and their anhydrides, halides, peroxides and peroxyacids; their halogenated, sulphonated, nitrated or nitrosated derivatives. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0%

Articles

Development of an enzyme-linked immunosorbent assay for the detection of the organophosphorus insecticide acephate.

J. Agric. Food Chem. 51(13) , 3695-703, (2003)

A competitive indirect enzyme-linked immunosorbent assay (ciELISA) for the organophosphorus insecticide acephate, O,S-dimethyl acetylphosphoramidothioate, was developed using a polyclonal antibody. Fi...

A thermostable L-aminoacylase from Thermococcus litoralis: cloning, overexpression, characterization, and applications in biotransformations.

Extremophiles 6(2) , 111-22, (2002)

A thermostable L-aminoacylase from Thermococcus litoralis was cloned, sequenced, and overexpressed in Escherichia coli. The enzyme is a homotetramer of 43 kDa monomers and has an 82% sequence identity...

Formation of high-aspect-ratio helical nanorods via chiral self-assembly of fullerodendrimers. Hilmer AJ, et al.

J. Phys. Chem. Lett. 5(5) , 929-34, (2014)


More Articles


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