V900667
2,3-Butanediol
Vetec™, reagent grade, 98%
Sinónimos:
2,3-Butylene glycol
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About This Item
Fórmula lineal:
CH3CH(OH)CH(OH)CH3
Número de CAS:
Peso molecular:
90.12
Beilstein:
969165
Número CE:
Número MDL:
Código UNSPSC:
12352100
ID de la sustancia en PubChem:
grado
reagent grade
Línea del producto
Vetec™
Ensayo
98%
índice de refracción
n20/D 1.433 (lit.)
bp
183-184 °C (lit.)
mp
25 °C (lit.)
densidad
1.002 g/mL at 20 °C (lit.)
cadena SMILES
CC(O)C(C)O
InChI
1S/C4H10O2/c1-3(5)4(2)6/h3-6H,1-2H3
Clave InChI
OWBTYPJTUOEWEK-UHFFFAOYSA-N
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Información legal
Vetec is a trademark of Merck KGaA, Darmstadt, Germany
Código de clase de almacenamiento
10 - Combustible liquids
Clase de riesgo para el agua (WGK)
WGK 1
Punto de inflamabilidad (°F)
185.0 °F - closed cup
Punto de inflamabilidad (°C)
85 °C - closed cup
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Natsuo Ueda et al.
Neuropharmacology, 48(8), 1079-1085 (2005-05-25)
It is widely accepted that fatty acid amide hydrolase (FAAH) plays a central role in the hydrolysis of anandamide. However, we found a second N-acylethanolamine hydrolase in animal tissues which hydrolyzed anandamide at acidic pH. This "acid amidase" was first
Frank Plaisant et al.
Free radical biology & medicine, 34(7), 862-872 (2003-03-26)
The pathophysiology of brain lesions associated with cerebral palsy is multifactorial and likely involves excess release of glutamate and excess production of free radicals, among other factors. Theoretically, antioxidants could limit the severity of these brain lesions. Peroxiredoxins are a
Patricia Hermand et al.
The Journal of biological chemistry, 278(7), 4892-4898 (2002-12-13)
ICAM-4 (LW blood group glycoprotein) is an erythroid-specific membrane component that belongs to the family of intercellular adhesion molecules and interacts in vitro with different members of the integrin family, suggesting a potential role in adhesion or cell interaction events
Zhi-Long Xiu et al.
Applied microbiology and biotechnology, 78(6), 917-926 (2008-03-06)
1,3-Propanediol and 2,3-butanediol are two promising chemicals which have a wide range of applications and can be biologically produced. The separation of these diols from fermentation broth makes more than 50% of the total costs in their microbial production. This
E Celińska et al.
Biotechnology advances, 27(6), 715-725 (2009-05-16)
Biotechnological production of 2,3-butanediol (hereafter referred to as 2,3-BD) from wastes and excessive biomass is a promising and attractive alternative for traditional chemical synthesis. In the face of scarcity of fossil fuel supplies the bio-based process is receiving a significant
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