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Merck
CN

55380

α-羟基异丁酸

puriss., ≥99.0% (HPLC)

别名:

2-甲基乳酸, 2-羟基-2-甲基丙酸

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线性分子式:
(CH3)2C(OH)COOH
化学文摘社编号:
分子量:
104.10
EC Number:
209-848-8
UNSPSC Code:
12352100
MDL number:
Beilstein/REAXYS Number:
1744739
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grade

puriss.

assay

≥99.0% (HPLC)

bp

84 °C/1.5 mmHg (lit.)

mp

76-80 °C (lit.), 78-81 °C

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

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pictograms

CorrosionExclamation mark

signalword

Danger

Hazard Classifications

Eye Dam. 1 - Skin Irrit. 2 - STOT SE 3

存储类别

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

法规信息

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M Bandell et al.
The Journal of biological chemistry, 275(50), 39130-39136 (2000-09-20)
The citrate transporter of Leuconostoc mesenteroides (CitP) catalyzes exchange of divalent anionic citrate from the medium for monovalent anionic lactate, which is an end product of citrate degradation. The exchange generates a membrane potential and thus metabolic energy for the
E Dadachova et al.
Applied radiation and isotopes : including data, instrumentation and methods for use in agriculture, industry and medicine, 48(4), 477-481 (1997-04-01)
We report the preliminary results from radiolabeling of a chelate-conjugated antibody with 166Ho produced from the beta(-)-decay of 166Dy. Ho-166 was separated from mg quantities of Dy target by reverse phase ion-exchange chromatography employing a cation exchange HPLC column and
Jeeyoun Jung et al.
Toxicology letters, 200(1-2), 1-7 (2010-10-12)
The dose-dependent perturbations in urinary metabolite concentrations caused by naproxen toxicity were investigated using ¹H NMR spectroscopy coupled with multivariate statistical analysis. Histopathologic evaluation of naproxen-induced acute gastrointestinal damage in rats demonstrated a significant dose-dependent effect. Furthermore, principal component analysis
Thore Rohwerder et al.
Microbial cell factories, 9, 13-13 (2010-02-27)
Nowadays a growing demand for green chemicals and cleantech solutions is motivating the industry to strive for biobased building blocks. We have identified the tertiary carbon atom-containing 2-hydroxyisobutyric acid (2-HIBA) as an interesting building block for polymer synthesis. Starting from
J D Pleil et al.
Biomarkers : biochemical indicators of exposure, response, and susceptibility to chemicals, 12(4), 331-348 (2007-06-15)
Adverse health risks from environmental agents are generally related to average (long-term) exposures. Because a given individual's contact with a pollutant is highly variable and dependent on activity patterns, local sources and exposure pathways, simple 'snapshot' measurements of surrounding environmental

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