This compound is miscible in water at a concentration of 50 µl/mL or approximately 47 µg/mL, based on a density of 0.935 g/mL. Solubility in other solvents, such as DMSO, has not been determined.
D183601
2,5-Dimethylpyrrole
98%
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5 G
$57.30
25 G
$111.00
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5 G
$57.30
25 G
$111.00
About This Item
Fórmula empírica (notación de Hill):
C6H9N
Número de CAS:
Peso molecular:
95.14
Número CE:
Número MDL:
Código UNSPSC:
12352100
ID de la sustancia en PubChem:
NACRES:
NA.22
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Nivel de calidad
Ensayo
98%
Formulario
liquid
índice de refracción
n20/D 1.505 (lit.)
bp
165 °C/740 mmHg (lit.)
densidad
0.935 g/mL at 25 °C (lit.)
cadena SMILES
Cc1ccc(C)[nH]1
InChI
1S/C6H9N/c1-5-3-4-6(2)7-5/h3-4,7H,1-2H3
Clave InChI
PAPNRQCYSFBWDI-UHFFFAOYSA-N
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Categorías relacionadas
Palabra de señalización
Danger
Frases de peligro
Clasificaciones de peligro
Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Eye Irrit. 2 - Flam. Liq. 3 - Skin Irrit. 2 - STOT SE 3
Órganos de actuación
Respiratory system
Código de clase de almacenamiento
3 - Flammable liquids
Clase de riesgo para el agua (WGK)
WGK 3
Punto de inflamabilidad (°F)
129.2 °F - closed cup
Punto de inflamabilidad (°C)
54 °C - closed cup
Equipo de protección personal
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
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M Zhu et al.
Journal of chromatography, 628(1), 37-47 (1993-01-01)
A method employing high-performance liquid chromatography with thermospray mass spectrometry (TSP-MS) and photodiode-array detection was developed and applied to the analysis of autoxidation products of 2,5-dimethyl-N-alkylpyrroles in aqueous solution under air or 18O2. Numerous oxidation products were separated, characterized and
Yoshiteru Matsumoto et al.
Physical chemistry chemical physics : PCCP, 13(31), 13962-13971 (2011-06-16)
N-H···π hydrogen-bonded (H-bonded) structures were studied by applying vibrational spectroscopy to self-aggregate clusters of 2,5-dimethylpyrrole (DMPy) and its binary clusters with pyrrole (Py). The NH stretching vibrations of jet-cooled clusters were observed by IR cavity ringdown spectroscopy. A combination of
Hongyin Yin et al.
PloS one, 8(9), e76011-e76011 (2013-10-08)
The formation of pyrrole adducts might be responsible for peripheral nerve injury caused by n-hexane. The internal dose of pyrrole adducts would supply more information for the neurotoxicity of n-hexane. The current study was designed to investigate the tissue distributions
Ireneusz Nowak et al.
Organic letters, 5(18), 3345-3348 (2003-08-29)
[reaction: see text] Protection of the amino group of adenine and guanine nucleosides was effected by heating the substrates in 2,5-hexanedione. The resulting 2,5-dimethylpyrrole adducts were stable toward bases but were hydrolyzed with TFA/H(2)O to regenerate the amino function.
Joseph M Beames et al.
The Journal of chemical physics, 131(17), 174305-174305 (2009-11-10)
The photophysical properties of porphyrins have relevance for their use as light-activated drugs in cancer treatment and sensitizers in solid-state solar cells. However, the appearance of their UV-visible spectra is usually explained inadequately by qualitative molecular-orbital theories. We intend to
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