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Documentos Principais

164976

Sigma-Aldrich

α-Hydroxyisobutyric acid

98%

Sinônimo(s):

alpha-Hydroxyisobutyric acid, 2-Hydroxy-2-methylpropionic acid, 2-Methyllactic acid

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About This Item

Fórmula linear:
(CH3)2C(OH)COOH
Número CAS:
Peso molecular:
104.10
Beilstein:
1744739
Número CE:
Número MDL:
Código UNSPSC:
12352100
ID de substância PubChem:
NACRES:
NA.22

Nível de qualidade

Ensaio

98%

forma

solid

pb

84 °C/1.5 mmHg (lit.)

pf

76-80 °C (lit.)

solubilidade

water: soluble 10%, clear to very slightly hazy, colorless

grupo funcional

carboxylic acid
hydroxyl

cadeia de caracteres SMILES

CC(C)(O)C(O)=O

InChI

1S/C4H8O3/c1-4(2,7)3(5)6/h7H,1-2H3,(H,5,6)

chave InChI

BWLBGMIXKSTLSX-UHFFFAOYSA-N

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Descrição geral

α-Hydroxyisobutyric acid (2-hydroxyisobutyric acid) is the building block for polymer synthesis. It forms complexes with Eu(III) and has been studied by time resolved fluorescence spectroscopy.

Aplicação

α-Hydroxyisobutyric acid was used as background electrolyte for separation and detection of the metal ions by on-line cyclic voltammetry.

Pictogramas

CorrosionExclamation mark

Palavra indicadora

Danger

Frases de perigo

Classificações de perigo

Eye Dam. 1 - Skin Irrit. 2 - STOT SE 3

Órgãos-alvo

Respiratory system

Código de classe de armazenamento

11 - Combustible Solids

Classe de risco de água (WGK)

WGK 3

Ponto de fulgor (°F)

Not applicable

Ponto de fulgor (°C)

Not applicable

Equipamento de proteção individual

dust mask type N95 (US), Eyeshields, Gloves


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Experimental factors in pulsed electrochemical detection in capillary electrophoresis.
Wen J, et al.
Journal of Chromatography A, 811(1), 181-192 (1998)
Nadya Yaneva et al.
The Journal of biological chemistry, 287(19), 15502-15511 (2012-03-22)
Coenzyme B(12)-dependent acyl-CoA mutases are radical enzymes catalyzing reversible carbon skeleton rearrangements in carboxylic acids. Here, we describe 2-hydroxyisobutyryl-CoA mutase (HCM) found in the bacterium Aquincola tertiaricarbonis as a novel member of the mutase family. HCM specifically catalyzes the interconversion
A Amberg et al.
Toxicological sciences : an official journal of the Society of Toxicology, 51(1), 1-8 (1999-09-25)
Methyl-tert-butyl ether (MTBE) is widely used as an additive to gasoline to increase oxygen content and reduce tail pipe emission of pollutants. Therefore, widespread human exposure may occur. To contribute to the characterization of potential adverse effects of MTBE, its
Ana Carolina O Costa et al.
Journal of chromatography. A, 1171(1-2), 140-143 (2007-10-09)
The aim of this work was to develop a fast method using capillary electrophoresis for the determination of creatinine in human urine samples. The pH and constituents of the background electrolyte were selected by inspection of effective mobility of creatinine
Thore Rohwerder et al.
Applied and environmental microbiology, 72(6), 4128-4135 (2006-06-06)
Fuel oxygenates such as methyl and ethyl tert-butyl ether (MTBE and ETBE, respectively) are degraded only by a limited number of bacterial strains. The aerobic pathway is generally thought to run via tert-butyl alcohol (TBA) and 2-hydroxyisobutyrate (2-HIBA), whereas further

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