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164976

Sigma-Aldrich

α-Hydroxyisobutyric acid

98%

Sinónimos:

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

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About This Item

Fórmula lineal:
(CH3)2C(OH)COOH
Número de CAS:
594-61-6
Peso molecular:
104.10
Beilstein/REAXYS Number:
1744739
EC Number:
209-848-8
MDL number:
MFCD00004459
UNSPSC Code:
12352100
PubChem Substance ID:
24850110
NACRES:
NA.22

Quality Level

100

assay

98%

form

solid

bp

84 °C/1.5 mmHg (lit.)

mp

76-80 °C (lit.)

solubility

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

functional group

carboxylic acid
hydroxyl

SMILES string

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

InChI

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

InChI key

BWLBGMIXKSTLSX-UHFFFAOYSA-N

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Categorías relacionadas

General description

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.

Application

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

pictograms

CorrosionExclamation mark
GHS05,GHS07

signalword

Danger

Hazard Classifications

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

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

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Certificados de análisis (COA)

Lot/Batch Number
MKBQ4931V
MKBP7730V
MKBP4403V
1446923
MKBK6109V

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Experimental factors in pulsed electrochemical detection in capillary electrophoresis.
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Journal of Chromatography A, 811(1), 181-192 (1998)
Thore Rohwerder et al.
Microbial cell factories, 9, 13-13 (2010-02-27)
Nowadays a growing demand for green chemicals and cleantech solutions is motivating the industry to strive for biobased building blocks. We have identified the tertiary carbon atom-containing 2-hydroxyisobutyric acid (2-HIBA) as an interesting building block for polymer synthesis. Starting from
Y Shigematsu et al.
Pediatric research, 16(9), 771-775 (1982-09-01)
Organic acids in plasma and urine of a patient with isovaleric acidemia were measured serially during a severe ketoacidotic attack. Urinary ketone bodies, lactic acid and 2-hydroxy-n-butyric acid changed in parallel with the plasma isovaleric acid concentration, which was correlated
A Jain et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 71(3), 1007-1010 (2008-04-15)
Complexation of Eu(III) with alpha-hydroxy isobutyric acid (HIBA), a model compound of humic acid, has been studied by time resolved fluorescence spectroscopy. The ratio of fluorescence intensity of the two peaks at 616 and 592 nm (I(616/592)) was found to
Susanta Lahiri et al.
Applied radiation and isotopes : including data, instrumentation and methods for use in agriculture, industry and medicine, 61(6), 1157-1161 (2004-09-25)
After irradiation with thermal neutrons 164Dy produces 166Ho through the nuclear reaction: 164Dy(n, gamma) 165Dy(n, gamma) 166Dy beta- --> 166Ho. 166Ho has been separated from the bulk dysprosium target with the help of HPLC using Aminex A7 ion exchanger resin
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