Usual Name 2-Hydroxyisobutyric acidCAS Number594-61-6Molecular Weight104.104Density1.2±0.1 g/cm3Boiling Point212.0±0.0 °C at 760 mmHgMolecular FormulaC4H8O3Melting Point76-80 °C(lit.)MSDSChineseUSAFlash Point104.9±16.3 °CSymbolGHS05, GHS07Signal WordDanger



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DensityBoiling PointMelting PointMolecular FormulaMolecular WeightFlash PointExact MassPSALogPVapour PressureIndex of Refraction
1.2±0.1 g/cm3
212.0±0.0 °C at 760 mmHg
76-80 °C(lit.)
C4H8O3
104.104
104.9±16.3 °C
104.047340
57.53000
-0.35
0.0±0.9 mmHg at 25°C
1.457

SymbolSignal WordHazard StatementsPrecautionary StatementsPersonal Protective EquipmentHazard Codes Risk PhrasesSafety PhrasesRIDADRWGK GermanyHS Code
GHS05, GHS07
Danger
H315-H318-H335
P261-P280-P305 + P351 + P338
dust mask type N95 (US);Eyeshields;Gloves
Xi:Irritant;
R41
S26-S39-S25
NONH for all settings of transport
3
2918199090

HS CodeSummary
2918199090
2918199090 various other carboxylic acids with alcohol function yet without other oxygen function, their anhydrides, halides, peroxides, peroxyacids and their derivatives。Supervision conditions:None。VAT:17.0%。Tax rebate rate:9.0%。MFN tariff:6.5%。General tariff:30.0%



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Thermophilic Coenzyme B12-Dependent Acyl Coenzyme A (CoA) Mutase from Kyrpidia tusciae DSM 2912 Preferentially Catalyzes Isomerization of (R)-3-Hydroxybutyryl-CoA and 2-Hydroxyisobutyryl-CoA.

Appl. Environ. Microbiol. 81 , 4564-72, (2015)

The recent discovery of a coenzyme B12-dependent acyl-coenzyme A (acyl-CoA) mutase isomerizing 3-hydroxybutyryl- and 2-hydroxyisobutyryl-CoA in the mesophilic bacterium Aquincola tertiaricarbonis L108...

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Capillary electrophoresis of little ions making use of facility formation and instraight detection.

Electrophoresis 30 Suppl 1 , S34-9, (2009)

The journal Electrophoresis was introduced in about the very same time as contemporary CE. Today, Electrophoresis is one of the leading journals in the area of analytical separations. With over 23% of all papers ...

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Solid-state and also solution-state coordination chemistry of lanthanide(III) complexes through α-hydroxyisobutyric acid.

Inorg. Chem. 51(24) , 13254-63, (2012)

Regardless of the wide variety of applications of α-hydroxyisobutyric acid (HIBA) in biochemical procedures, pharmaceutical formulations, and also group and elemental separations of lanthanides and also actinides, the s...

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