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经验公式(希尔记法):
C5H8N2
化学文摘社编号:
分子量:
96.13
NACRES:
NA.22
PubChem Substance ID:
eCl@ss:
39160503
UNSPSC Code:
12352100
EC Number:
200-657-5
MDL number:
Beilstein/REAXYS Number:
106325
Assay:
≥99.0% (GC)
产品名称
3,5-二甲基吡唑, Wacker Chemie AG, ≥99.0% (GC)
InChI
1S/C5H8N2/c1-4-3-5(2)7-6-4/h3H,1-2H3,(H,6,7)
InChI key
SDXAWLJRERMRKF-UHFFFAOYSA-N
SMILES string
Cc1cc(C)[nH]n1
assay
≥99.0% (GC)
manufacturer/tradename
Wacker Chemie AG
bp
218 °C (lit.)
mp
105-108 °C (lit.)
Quality Level
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signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral - STOT RE 2
target_organs
Liver
存储类别
13 - Non Combustible Solids
wgk
WGK 3
ppe
dust mask type N95 (US), Eyeshields, Gloves
Gabriella Cavallini et al.
Autophagy, 3(1), 26-27 (2006-09-12)
Autophagy is a major intracellular degradation/recycling system ubiquitous in eukaryotic cells. It contributes to the turnover of cellular components by delivering portions of the cytoplasm and organelles to lysosomes, where they are digested. Starvation-induced autophagy is required for maintaining an
Alessandra Del Roso et al.
Experimental gerontology, 38(5), 519-527 (2003-05-14)
Autophagy is a universal, highly regulated mechanism responsible for the degradation of long-lived proteins, cytomembranes and organelles during fasting and may be the cell repair mechanism that mediates the anti-ageing effects of calorie restriction (Bergamini and Gori, 1995). The function
E Bergamini et al.
The American journal of physiology, 266(1 Pt 1), G118-G122 (1994-01-01)
Regulation of liver macroautophagy and protein degradation by hormones and direct regulatory amino acids were studied in male 2-mo-old Sprague-Dawley albino rats with the use of the antilipolytic agent 3,5'-dimethylpyrazole (DMP; 12 mg/kg body wt ip) as a stimulatory agent.
C Redekopp et al.
Journal of endocrinological investigation, 7(4), 277-281 (1984-08-01)
The inhibitory and stimulatory effects of somatostatin analogues on growth hormone secretion have been studied in the sheep. Plasma immunoreactive growth hormone (GH) was stimulated by the iv administration of the antilipolytic compound 3,5-dimethylpyrazole and was followed by infusion of
J M Orza et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 56A(8), 1469-1498 (2000-07-25)
The infrared (IR) and Raman spectra of 3,5-dimethylpyrazole have been recorded in the vapor, liquid (melt and solution) and solid states. Two deuterated derivatives, C5H7N-ND and C5D7N-NH, were also studied in solid state and in solutions. Instrumental resolution was relatively
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