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20487-40-5

20487-40-5 Structure

20487-40-5 Structure
IdentificationBack Directory
[Name]

TERT-BUTYL PROPIONATE
[CAS]

20487-40-5
[Synonyms]

Stain a
C2H5C(O)OC(CH3)3
t-Butyl propanoate
t-Butyl propionate
ert-butylpropanoate
tert-butyl propanoate
TERT-BUTYL PROPIONATE
tert-Butyl Propionate >
tert-Butyl propionate 99%
1,1-DIMETHYLETHYLPROPIONATE
1,1-Dimethylethylpropanoate
tert-Butyl Propionate
Propionic acid, tert-butyl ester
Propionic acid 1,1-dimethylethyl ester
Propanoic acid, 1,1-dimethylethyl ester
Propionic acid 2-methylpropan-2-yl ester
TERT-BUTYL PROPIONATE ISO 9001:2015 REACH
[EINECS(EC#)]

238-424-5
[Molecular Formula]

C7H14O2
[MDL Number]

MFCD00009304
[MOL File]

20487-40-5.mol
[Molecular Weight]

130.18
Chemical PropertiesBack Directory
[Melting point ]

-80.46°C (estimate)
[Boiling point ]

118-118.5 °C (lit.)
[density ]

0.865 g/mL at 25 °C (lit.)
[refractive index ]

n20/D 1.393(lit.)
[Fp ]

21 °C
[storage temp. ]

Store at room temperature
[form ]

clear liquid
[color ]

Colorless to Almost colorless
[BRN ]

1747857
[InChI]

1S/C7H14O2/c1-5-6(8)9-7(2,3)4/h5H2,1-4H3
[InChIKey]

JAELLLITIZHOGQ-UHFFFAOYSA-N
[SMILES]

CCC(=O)OC(C)(C)C
[LogP]

2.059 (est)
Questions And AnswerBack Directory
[Uses]

tert-butyl propionate can be used as a solvent for nitrocellulose, fragrances, and flavorings. It is a solvent for nitrocellulose, natural and synthetic resins, and can be used as a solvent for paints. It is also used in the manufacture of fragrances.
Safety DataBack Directory
[Hazard Codes ]

F,Xi
[Risk Statements ]

10-36/37/38-11
[Safety Statements ]

16-36/37/39-26
[RIDADR ]

UN 2394 3/PG 3
[WGK Germany ]

2
[RTECS ]

UF4930000
[HS Code ]

2915.50.5000
[HazardClass ]

3.1
[PackingGroup ]

II
[Storage Class]

3 - Flammable liquids
[Hazard Classifications]

Eye Irrit. 2
Flam. Liq. 2
Skin Irrit. 2
Spectrum DetailBack Directory
[Spectrum Detail]

TERT-BUTYL PROPIONATE(20487-40-5)1HNMR
TERT-BUTYL PROPIONATE(20487-40-5)FT-IR
TERT-BUTYL PROPIONATE(20487-40-5)Raman
TERT-BUTYL PROPIONATE(20487-40-5)IR
Hazard InformationBack Directory
[General Description]

Stereochemistry of kinetic Michael addition of the Z and E lithium enolates of tert-butyl propionate has been investigated.
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