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Merck

T133

Sigma-Aldrich

Inactin® hydrate

≥98% (HPLC)

Sinónimos:

Thiobutabarbital sodium salt hydrate

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About This Item

Fórmula empírica (notación de Hill):
C10H15N2NaO2S · xH2O
Número de CAS:
Peso molecular:
250.29 (anhydrous basis)
Número CE:
Número MDL:
Código UNSPSC:
12352200
ID de la sustancia en PubChem:
NACRES:
NA.77
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Nivel de calidad

Ensayo

≥98% (HPLC)

Formulario

powder

control farmacológico

USDEA Schedule IIIN; regulated under CDSA - not available from Sigma-Aldrich Canada

color

light yellow

solubilidad

H2O: soluble (storage of solutions for more than 8 hours at 4°C is not recommended.)

cadena SMILES

[Na+].CCC(C)C1(CC)C([O-])=NC(=S)NC1=O

InChI

1S/C10H16N2O2S.Na/c1-4-6(3)10(5-2)7(13)11-9(15)12-8(10)14;/h6H,4-5H2,1-3H3,(H2,11,12,13,14,15);/q;+1/p-1

Clave InChI

SLZHLQUFNFXTHB-UHFFFAOYSA-M

Aplicación

Inactin® hydrate has been used to anesthetize rats to study stress-induced hypersensitivity[1] and mice to study Cisplatin-induced neuropathy.[2] It has also been used to anesthetize rats to measure the glomerular filtration rate (GFR).[3]

Acciones bioquímicas o fisiológicas

Inactin® is a long-lasting rodent anesthetic with minimal effects on cardiovascular tone and renal output. It exhibits sedative and hypnotic properties.

Información legal

Inactin is a registered trademark of Merck KGaA, Darmstadt, Germany

Código de clase de almacenamiento

11 - 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

Eyeshields, Gloves, type N95 (US)


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Visite la Librería de documentos

Flecknell
Laboratory Animal Anesthesia. An introduction for Research Workers and Technicians, 36-36 (1987)
Min-Suk Yoon et al.
BMC neuroscience, 10, 77-77 (2009-07-16)
Cisplatin mediates its antineoplastic activity by formation of distinct DNA intrastrand cross links. The clinical efficacy and desirable dose escalations of cisplatin are restricted by the accumulation of DNA lesions in dorsal root ganglion (DRG) cells leading to sensory polyneuropathy
Maki Niihori et al.
American journal of respiratory cell and molecular biology, 62(2), 231-242 (2019-08-29)
NFU1 is a mitochondrial protein that is involved in the biosynthesis of iron-sulfur clusters, and its genetic modification is associated with disorders of mitochondrial energy metabolism. Patients with autosomal-recessive inheritance of the NFU1 mutation G208C have reduced activity of the
Eman Y Gohar et al.
Journal of the American Heart Association, 9(10), e015110-e015110 (2020-05-12)
Background The novel estrogen receptor, G-protein-coupled estrogen receptor (GPER), is responsible for rapid estrogen signaling. GPER activation elicits cardiovascular and nephroprotective effects against salt-induced complications, yet there is no direct evidence for GPER control of renal Na+ handling. We hypothesized
Haiyun Qi et al.
Magnetic resonance in medicine, 80(5), 2073-2080 (2018-03-10)
Anesthesia is necessary for most animal studies requiring invasive procedures. It is well documented that various types of anesthesia modulate a wide variety of important metabolic and functional processes in the body, and as such, represent a potential limitation in

Questions

  1. How should item T133, Inactin® hydrate be reconstituted and stored?

    1 answer
    1. Item T133, Inactin® hydrate, is soluble in water. According to our website, after reconstitution in water, storing solutions for more than 8 hours at 4°C is not recommended.

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