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05091

3,5-Dimethylpyrazole

Name: 3,5-Dimethylpyrazole
Brand: SIAL

Wacker Chemie AG, ≥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

NACRES:

NA.22

PubChem Substance ID:

329748042

eCl@ss:

39160503

UNSPSC Code:

12352100

EC Number:

200-657-5

MDL number:

MFCD00005243

Beilstein/REAXYS Number:

106325

Assay:

≥99.0% (GC)

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Properties

Quality Segment

100

assay

≥99.0% (GC)

manufacturer/tradename

Wacker Chemie AG

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

Description

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pictograms

GHS08,GHS07

signalword

Warning

hcodes

H302,H373

pcodes

P260 - P264 - P270 - P301 + P312 - P314 - P501

Hazard Classifications

Acute Tox. 4 Oral - STOT RE 2

target_organs

Liver

Storage Class

13 - Non Combustible Solids

wgk

WGK 3

ppe

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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Vibrational spectra of 3,5-dimethylpyrazole and deuterated derivatives.

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

Stimulation of autophagy by antilipolytic drugs may rescue rodents from age-associated hypercholesterolemia.

Sara Straniero et al.

Rejuvenation research, 12(2), 77-84 (2009-05-08)

Aging is characterized by several metabolic changes responsible for the decline of certain functions and the appearance of age-related diseases, including hypercholesterolemia, which is the main risk factor for atherosclerosis and cardiovascular disease. Similar changes in a number of morphological

Effects of antilipolytic agents on rat liver peroxisomes and peroxisomal oxidative activities.

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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Global Trade Item Number

SKU	GTIN
R0875-1G	04061836694005
5061300001	04055977243123
55842-5ML	04061838592569
83580-5G	04061833005767
PHR1750-1G	04061834802273
R0200000	04061836693756
06859-50MG	04061838647061
83580-1G	04061833005750
43530-4.5ML-F	04061832113531
1601000-200MG	04061838744999
05091-25KG-F	04061832993119
05091-100G-F	04061838636751
05091-1KG-F	04061826197776