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Merck

32002

Sigma-Aldrich

Sodium 5,5-diethylbarbiturate

purum, ≥99.0% (NT)

Sinónimos:

5,5-Diethylbarbituric acid sodium salt, Barbitone, Sodium barbital, Veronal sodium salt

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About This Item

Fórmula empírica (notación de Hill):
C8H11N2NaO3
Número de CAS:
Peso molecular:
206.17
Beilstein:
3921202
Número CE:
Número MDL:
Código UNSPSC:
12161703
ID de la sustancia en PubChem:
NACRES:
NA.77

grado

purum

Nivel de calidad

Ensayo

≥99.0% (NT)

Formulario

powder or crystals

control farmacológico

regulated under CDSA - not available from Sigma-Aldrich Canada; psicótropo (Spain); Decreto Lei 15/93: Tabela IV (Portugal)

condiciones de almacenamiento

(Tightly closed. Dry.)

técnicas

GC/MS: suitable
HPLC: suitable
activity assay: suitable

color

colorless

pH

9.0-10.5

mp

>287.1 °C (> 548.8 °F)

solubilidad

water: soluble 103.1 g/L at 20 °C (68 °F)

densidad

1.418 g/cm3 at 20 °C ( 68 °F)

idoneidad

suitable for microbiology
suitable for molecular biology

aplicaciones

cell analysis

cadena SMILES

[Na+].CCC1(CC)C(=O)NC([O-])=NC1=O

InChI

1S/C8H12N2O3.Na/c1-3-8(4-2)5(11)9-7(13)10-6(8)12;/h3-4H2,1-2H3,(H2,9,10,11,12,13);/q;+1/p-1

Clave InChI

RGHFKWPGWBFQLN-UHFFFAOYSA-M

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Descripción general

Sodium 5,5-diethyl barbiturate, also known as Barbital sodium, is a long-acting barbiturate that can significantly depress various metabolic processes at high doses. This weak acid has widespread applications in scientific fields, particularly as a buffering solution in biochemical and biological experiments due to its buffering capabilities. It is particularly well-suited for scenarios requiring lower buffer capacity without compromising pH stability. This buffering effect is achieved through the equilibrium between the acid and its corresponding anion, effectively stabilizing the pH within the desired range. Additionally, Sodium 5,5-diethyl barbiturate has potential applications in histology, and biochemical research, including uses in enzyme assays, cell structure staining, and electrophoresis.

Aplicación

Sodium 5,5-diethyl barbiturate has been used as a component of Michaeli′s buffer, a commonly used buffer solution that helps maintain ideal conditions for histological and histopathological analyses. It is also utilized as a biological buffer in immunoelectrophoresis, hemolytic assays and fixative solutions.

Acciones bioquímicas o fisiológicas

Sedative/hypnotic

Características y beneficios

  • Suitable for electrophoresis and enzymatic assays
  • High purity product for research applications
  • Component of Michaeli′s buffer

Advertencia

Substance of abuse. Regulatory approval may be required for purchase. Comply with applicable laws. Exercise responsible use.

Otras notas

For additional information on our range of Biochemicals, please complete this form.
This product is intended for research purposes only, and it is not meant for human consumption.
Sales restrictions may apply

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Referencia del producto
Descripción
Precios

Pictogramas

Health hazardExclamation mark

Palabra de señalización

Warning

Clasificaciones de peligro

Acute Tox. 4 Oral - Eye Irrit. 2 - Repr. 2 - Skin Irrit. 2 - STOT SE 2 - STOT SE 3

Órganos de actuación

Nervous system, Respiratory system

Código de clase de almacenamiento

13 - Non Combustible Solids

Clase de riesgo para el agua (WGK)

WGK 3

Punto de inflamabilidad (°F)

Not applicable

Punto de inflamabilidad (°C)

Not applicable

Equipo de protección personal

dust mask type N95 (US), Eyeshields, Faceshields, Gloves


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Visite la Librería de documentos

C S Rinder et al.
The Journal of clinical investigation, 96(3), 1564-1572 (1995-09-01)
Complement activation contributes to the systemic inflammatory response induced by cardiopulmonary bypass. At the cellular level, cardiopulmonary bypass activates leukocytes and platelets; however the contribution of early (3a) versus late (C5a, soluble C5b-9) complement components to this activation is unclear.
Y Hiasa et al.
Carcinogenesis, 3(10), 1187-1190 (1982-01-01)
Phenobarbital (PB) and barbital (BB) promoted the development of thyroid tumors in rats treated with a sub-effective dose of N-bis(2-hydroxypropyl)nitrosamine (DHPN) for thyroid tumorigenesis. Rats were given s.c. injections of 70 mg DHPN/100 g body weight once a week for

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