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05091

Sigma-Aldrich

3,5-Dimethylpyrazole

produced by Wacker Chemie AG, Burghausen, Germany, ≥99.0% (GC)

Synonym(s):

3,5-Dimethyl-1H-pyrazole

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About This Item

Empirical Formula (Hill Notation):
C5H8N2
CAS Number:
67-51-6
Molecular Weight:
96.13
Beilstein:
106325
EC Number:
200-657-5
MDL number:
MFCD00005243
UNSPSC Code:
12352100
eCl@ss:
39160503
PubChem Substance ID:
329748042
NACRES:
NA.22

grade

produced by Wacker Chemie AG, Burghausen, Germany

Quality Level

100

Assay

≥99.0% (GC)

bp

218 °C (lit.)

mp

105-108 °C (lit.)

SMILES string

Cc1cc(C)[nH]n1

InChI

1S/C5H8N2/c1-4-3-5(2)7-6-4/h3H,1-2H3,(H,6,7)

InChI key

SDXAWLJRERMRKF-UHFFFAOYSA-N

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Pictograms

Health hazardExclamation mark
GHS08,GHS07

Signal Word

Warning

Hazard Statements

H302,H373

Hazard Classifications

Acute Tox. 4 Oral - STOT RE 2

Target Organs

Liver

Storage Class Code

13 - Non Combustible Solids

WGK

WGK 3

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
BCCM2282
BCBR1242V
BCCF3488

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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.
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.
Experimental and molecular pathology, 46(1), 114-122 (1987-02-01)
A dramatic increase in the plasma glucagon/insulin ratio can be induced by treating fasted rats with antilipolytic drugs (e.g., with 3,5-dimethylpyrazole, 12 mg/kg body wt). These hormone changes are the physiologically appropriate response to a rapid decrease in free fatty
Rupam Sarma et al.
Dalton transactions (Cambridge, England : 2003), (36)(36), 7428-7436 (2009-09-04)
The reactions of 3,5-dimethylpyrazole with zinc(II)acetate dihydrate and varieties of aromatic carboxylic acids led to formation of mono-nuclear zinc complexes of composition [Zn(HDMP)2(RCO2)2] (R = C6H5, p-CH3-C6H4, p-NO2-C6H4 etc. HDMP = 3,5-dimethylpyrazole) in methanol, whereas the same reactants in dimethylformamide
T Locci Cubeddu et al.
Biochimica et biophysica acta, 839(1), 96-104 (1985-03-29)
The mechanisms involved in the inhibitory effects of antilipolytic agents on rat liver peroxisomal fatty acid oxidative activity have been explored. Treatment of fasting rats with antilipolytic drugs (either 3,5-dimethylpyrazole (12 mg/kg body weight) or Acipimox (25 mg/kg body weight]
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