323594
α-Hydroxyisobutyric acid
99%
Synonyme(s) :
alpha-Hydroxyisobutyric acid, 2-Hydroxy-2-methylpropionic acid, 2-Methyllactic acid
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A propos de cet article
Formule linéaire :
(CH3)2C(OH)COOH
Numéro CAS:
Poids moléculaire :
104.10
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
209-848-8
Beilstein/REAXYS Number:
1744739
MDL number:
Assay:
99%
Form:
solid
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assay
99%
form
solid
bp
84 °C/1.5 mmHg (lit.)
mp
76-80 °C (lit.)
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
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
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.
signalword
Danger
hcodes
Hazard Classifications
Eye Dam. 1 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Classe de stockage
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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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)
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)
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)