Direkt zum Inhalt
Merck

32002

Sigma-Aldrich

Natrium-5,5-diethylbarbiturat

purum, ≥99.0% (NT)

Synonym(e):

5,5-Diethylbarbitursäure Natriumsalz, Natriumbarbital, Veronal

Anmeldenzur Ansicht organisationsspezifischer und vertraglich vereinbarter Preise


About This Item

Empirische Formel (Hill-System):
C8H11N2NaO3
CAS-Nummer:
Molekulargewicht:
206.17
Beilstein:
3921202
EG-Nummer:
MDL-Nummer:
UNSPSC-Code:
12161703
PubChem Substanz-ID:
NACRES:
NA.77

Qualität

purum

Qualitätsniveau

Assay

≥99.0% (NT)

Form

powder or crystals

Arzneimittelkontrolle

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

Lagerbedingungen

(Tightly closed. Dry.)

Methode(n)

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

Farbe

colorless

pH-Wert

9.0-10.5

mp (Schmelzpunkt)

>287.1 °C (> 548.8 °F)

Löslichkeit

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

Dichte

1.418 g/cm3 at 20 °C ( 68 °F)

Eignung

suitable for microbiology
suitable for molecular biology

Anwendung(en)

cell analysis

SMILES String

[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

InChIKey

RGHFKWPGWBFQLN-UHFFFAOYSA-M

Suchen Sie nach ähnlichen Produkten? Aufrufen Leitfaden zum Produktvergleich

Allgemeine Beschreibung

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.

Anwendung

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.

Biochem./physiol. Wirkung

beruhigend/hypnotisch

Leistungsmerkmale und Vorteile

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

Warnhinweis

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

Sonstige Hinweise

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

Vergleichbares Produkt

Produkt-Nr.
Beschreibung
Preisangaben

Piktogramme

Exclamation markHealth hazard

Signalwort

Warning

Gefahreneinstufungen

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

Zielorgane

Nervous system, Respiratory system

Lagerklassenschlüssel

13 - Non Combustible Solids

WGK

WGK 3

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable

Persönliche Schutzausrüstung

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


Hier finden Sie alle aktuellen Versionen:

Analysenzertifikate (COA)

Lot/Batch Number

Die passende Version wird nicht angezeigt?

Wenn Sie eine bestimmte Version benötigen, können Sie anhand der Lot- oder Chargennummer nach einem spezifischen Zertifikat suchen.

Besitzen Sie dieses Produkt bereits?

In der Dokumentenbibliothek finden Sie die Dokumentation zu den Produkten, die Sie kürzlich erworben haben.

Die Dokumentenbibliothek aufrufen

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

Unser Team von Wissenschaftlern verfügt über Erfahrung in allen Forschungsbereichen einschließlich Life Science, Materialwissenschaften, chemischer Synthese, Chromatographie, Analytik und vielen mehr..

Setzen Sie sich mit dem technischen Dienst in Verbindung.