- 2-Hydroxyisobutyric acid
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- $50.00
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2026-07-02
- CAS:594-61-6
- Min. Order: 1kg
- Purity: 99%,Electronic grade(Single metal impurity≤ 10ppb)
- Supply Ability: 100kg
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| | 2-Hydroxyisobutyric acid Basic information |
| | 2-Hydroxyisobutyric acid Chemical Properties |
| Melting point | 76-80 °C(lit.) | | Boiling point | 84 °C1.5 mm Hg(lit.) | | density | 11412 | | refractive index | 1.4761 (estimate) | | Fp | 114°C/12mm | | storage temp. | Sealed in dry,Room Temperature | | solubility | water: soluble10%, clear to very slightly hazy, colorless | | pka | pK1:3.717 (25°C,μ=0.1) | | form | Solid | | color | White to Off-White | | Water Solubility | Soluble in water, ether, alcohol, methanol and hot benzene. | | BRN | 1744739 | | Cosmetics Ingredients Functions | FRAGRANCE | | InChI | 1S/C4H8O3/c1-4(2,7)3(5)6/h7H,1-2H3,(H,5,6) | | InChIKey | BWLBGMIXKSTLSX-UHFFFAOYSA-N | | SMILES | CC(C)(O)C(O)=O | | LogP | -0.360 | | CAS DataBase Reference | 594-61-6(CAS DataBase Reference) | | NIST Chemistry Reference | Propanoic acid, 2-hydroxy-2-methyl-(594-61-6) | | EPA Substance Registry System | Propanoic acid, 2-hydroxy-2-methyl- (594-61-6) |
| Hazard Codes | Xi | | Risk Statements | 37/38-41-36/37/38 | | Safety Statements | 26-39-25-36 | | WGK Germany | 3 | | Hazard Note | Irritant | | TSCA | TSCA listed | | HS Code | 29181980 | | Storage Class | 11 - Combustible Solids | | Hazard Classifications | Eye Dam. 1 Skin Irrit. 2 STOT SE 3 |
| | 2-Hydroxyisobutyric acid Usage And Synthesis |
| Chemical Properties | white to off-white needle-like crystals or | | Uses | 2-Hydroxyisobutyric acid is used as background electrolyte for separation and detection of the metal ions by on-line cyclic voltammetry. | | Uses | 2-Hydroxyisobutyric acid is used as an electrolyte in the separation of the metal ions by on-line cyclic voltammetry. It is also used as a building block for the synthesis of polymers. Its conjugate base, 2-hydroxybutyrate is utilized to catabolize L-threonine as well as synthesize glutathione. Further, it is used as an indicator for the early detection insulin resistance in non-diabetic subjects. | | Uses | α-Hydroxyisobutyric acid was used as background electrolyte for separation and detection of the metal ions by on-line cyclic voltammetry. | | Definition | ChEBI: A 2-hydroxy monocarboxylic acid that is isobutyric acid bearing a hydroxy substituent at position 2. It is a metabolite of methyl tertiary-butyl ether. | | Synthesis Reference(s) | The Journal of Organic Chemistry, 23, p. 1488, 1958 DOI: 10.1021/jo01104a022 | | 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. |
| | 2-Hydroxyisobutyric acid Preparation Products And Raw materials |
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