H40009
2-羟基-2-甲基丁酸
98%
别名:
α-Hydroxy-α-methylbutyric acid, (±)-α-Hydroxy-α-methylbutyric acid, (±)-2-Hydroxy-2-methylbutanoic acid, (±)-2-Hydroxy-2-methylbutyric acid, 2-Hydroxy-2-methylbutanoic acid, 2-Methyl-2-hydroxybutyric acid
登录查看公司和协议定价
所有图片(1)
About This Item
线性分子式:
C2H5C(CH3)(OH)CO2H
CAS号:
分子量:
118.13
EC號碼:
MDL號碼:
分類程式碼代碼:
12352100
PubChem物質ID:
NACRES:
NA.22
推荐产品
品質等級
化驗
98%
mp
73-75 °C (lit.)
SMILES 字串
CCC(C)(O)C(O)=O
InChI
1S/C5H10O3/c1-3-5(2,8)4(6)7/h8H,3H2,1-2H3,(H,6,7)
InChI 密鑰
MBIQENSCDNJOIY-UHFFFAOYSA-N
應用
2-Hydroxy-2-methylbutyric acid can be used as:
- A complexing agent in a new electrolytic system, applicable in the isotachophoretic lanthanide separation.
- An aldehyde surrogate to prepare pyrrolo[1,2-a]quinoxaline derivatives by reacting with 2-(1H-pyrrol-1-yl)aniline.
- A starting material to synthesize Cr(V) reagent named sodium bis(2-hydroxy-2-methylbutyrato)oxochromate(V) (Aldrich cat. no. ALD00006) applicable in the total synthesis of (−)-taxuyunnanine D.
訊號詞
Warning
危險分類
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
標靶器官
Respiratory system
儲存類別代碼
11 - Combustible Solids
水污染物質分類（WGK）
WGK 3
閃點（°F）
Not applicable
閃點（°C）
Not applicable
個人防護裝備
dust mask type N95 (US), Eyeshields, Gloves
其他客户在看
Separation and analysis of lanthanides by isotachophoresis coupled with inductively coupled plasma mass spectrometry
Vio L, et al.
Talanta, 99, 586-593 (2012)
Two-phase synthesis of (−)-taxuyunnanine D
Wilde NC, et al.
Journal of the American Chemical Society, 136(13), 4909-4912 (2014)
Florence Guéguen et al.
Talanta, 162, 278-284 (2016-11-14)
The high-precision isotopic characterization of actinides and fission products in nuclear samples is fundamental for various applications such as the management of spent nuclear fuel or the validation of neutronic calculation codes. However multi-elemental isotope ratio measurements by mass spectrometric
W Dekant et al.
Research report (Health Effects Institute), (102)(102), 29-71 (2001-08-16)
The biotransformation of methyl tert-butyl ether (MTBE), ethyl tert-butyl ether (ETBE), and tert-amyl methyl ether (TAME) was studied in humans and in rats after inhalation of 4 and 40 ppm of MTBE, ETBE, and TAME, respectively, for 4 hours, and
α-Hydroxy acid as an aldehyde surrogate: metal-free synthesis of pyrrolo [1, 2-a] quinoxalines, quinazolinones, and other N-heterocycles via decarboxylative oxidative annulation reaction
Viji M, et al.
Royal Society of Chemistry Advances, 10(61), 37202-37208 (2020)
我们的科学家团队拥有各种研究领域经验，包括生命科学、材料科学、化学合成、色谱、分析及许多其他领域.
联系技术服务部门