signalword
Danger
flash_point_f
Not applicable
flash_point_c
Not applicable
target_organs
Central nervous system, thymus,Liver
hcodes
Hazard Classifications
Acute Tox. 4 Dermal - Eye Dam. 1 - Met. Corr. 1 - Skin Corr. 1B - STOT RE 1 Dermal - STOT SE 1
存储类别
6.1D - Non-combustible acute toxic Cat.3 / toxic hazardous materials or hazardous materials causing chronic effects
法规信息
新产品
此项目有
Ngoc-Duc Doan et al.
Biopolymers, 104(5), 629-635 (2015-03-20)
The conformation of the N-amino-imidazolidin-2-one (Aid) peptidomimetic was investigated using NMR spectroscopy and X-ray crystallography. In solution, the tetrapeptide model p-bromobenzoyl-Aid-l-Phe-N'-iso-propylamide (1) exhibited shielded and solvent exposed amide protons indicative of a turn conformation. In the crystal lattice of 1
T Michael De Silva et al.
Hypertension (Dallas, Tex. : 1979), 65(2), 345-351 (2014-11-12)
Myogenic responses by resistance vessels are a key component of autoregulation in brain, thus playing a crucial role in regulating cerebral blood flow and protecting the blood-brain barrier against potentially detrimental elevations in blood pressure. Although cerebrovascular disease is often
Sebastiaan Bijttebier et al.
Food chemistry, 163, 147-153 (2014-06-11)
Alkaline saponification is often used to remove interfering chlorophylls and lipids during carotenoids analysis. However, saponification also hydrolyses esterified carotenoids and is known to induce artifacts. To avoid carotenoid artifact formation during saponification, Larsen and Christensen (2005) developed a gentler
Jiannan Sun et al.
Journal of chromatography. A, 1379, 112-117 (2015-01-13)
This study achieved resolution improvement for iodine speciation in the presence of an ion-pairing reagent by a pressure-driven capillary electrophoresis (CE) system. Addition of 0.01mM tetrabutyl ammonium hydroxide (TBAH) as the ion-pairing reagent into the electrophoretic buffer resulted in the
Xueyan Zheng et al.
Carbohydrate polymers, 111, 25-32 (2014-07-20)
Tetraalkylammonium hydroxides have been found to mediate regioselective deacylation of cellulose esters. This deacylation surprisingly shows substantial selectivity for the removal of the acyl groups at O-2/3, affording cellulose-6-O-esters by a simple, efficient one-step process. The mechanism for this deacylation
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