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About This Item
Linear Formula:
(CH3)2C(OH)COOH
CAS Number:
Molecular Weight:
104.10
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
209-848-8
Beilstein/REAXYS Number:
1744739
MDL number:
Product Name
α-Hydroxyisobutyric acid, 99%
InChI key
BWLBGMIXKSTLSX-UHFFFAOYSA-N
InChI
1S/C4H8O3/c1-4(2,7)3(5)6/h7H,1-2H3,(H,5,6)
SMILES string
CC(C)(O)C(O)=O
assay
99%
form
solid
bp
84 °C/1.5 mmHg (lit.)
mp
76-80 °C (lit.)
functional group
carboxylic acid
hydroxyl
Quality Level
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Application
α-Hydroxyisobutyric acid (HIBA) can be used as:
- A chelating agent to improve the separation of lanthanides and actinides by liquid chromatography.
- In the synthesis of room temperature–stabilized, pure, nanocrystalline β-NiMoO4.
General description
α-Hydroxyisobutyric acid is a versatile building block in organic synthesis. It serves as a precursor in the synthesis of compounds like isobutylene glycol and methacrylic acid
signalword
Danger
hcodes
Hazard Classifications
Eye Dam. 1 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
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Bimetallic single-source precursor for the synthesis of pure nanocrystalline room temperature-stabilized β-NiMoO4
Moneeb AM, et al.
Ceramics International, 42(1), 1366-1372 (2016)
Electrospray ionization mass spectrometric studies on uranyl complex with α-hydroxyisobutyric acid in water-methanol medium
Jaison PG, et al.
Rapid Communications in Mass Spectrometry, 27(10), 1105-1118 (2013)
From rotational resolved spectra to an extended increment system of planar moments allowing ad-hoc conformational identification ? Exemplification by the broadband microwave spectrum of ??- hydroxyisobutyric acid
P Buschmann, et al.
Journal of Molecular Structure, 1250, 131805-131805 (2022)
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
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