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Merck

323594

α-Hydroxyisobutyric acid

99%

Synonym(s):

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

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About This Item

Linear Formula:
(CH3)2C(OH)COOH
CAS Number:
594-61-6
Molecular Weight:
104.10
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
24859404
EC Number:
209-848-8
Beilstein/REAXYS Number:
1744739
MDL number:
MFCD00004459

Key Documents

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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

200

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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

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

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
MKCZ9029
MKCZ4201
MKCZ3321
MKCV6236
WXBF0205V

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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)
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
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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