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Documentos Principais

D0513

Supelco

Dibucaine

analytical standard

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About This Item

Fórmula empírica (Notação de Hill):
C20H29N3O2
Número CAS:
Peso molecular:
343.46
Número CE:
Número MDL:
Código UNSPSC:
41116107
ID de substância PubChem:

grau

analytical standard

técnica(s)

HPLC: suitable
gas chromatography (GC): suitable

aplicação(ões)

cleaning products
cosmetics
food and beverages
forensics and toxicology
personal care
pharmaceutical (small molecule)
veterinary

formato

neat

cadeia de caracteres SMILES

CCCCOc1cc(C(=O)NCCN(CC)CC)c2ccccc2n1

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Aplicação

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Ações bioquímicas/fisiológicas

Potent, long-acting local anesthetic

Pictogramas

Environment

Frases de perigo

Declarações de precaução

Classificações de perigo

Aquatic Chronic 2

Código de classe de armazenamento

11 - Combustible Solids

Classe de risco de água (WGK)

WGK 3

Ponto de fulgor (°F)

Not applicable

Ponto de fulgor (°C)

Not applicable

Equipamento de proteção individual

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


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A Seelig
Cell biology international reports, 14(4), 369-380 (1990-04-01)
The interaction between lipids and water soluble amphiphiles was investigated by means of a monolayer technique, monitoring the area increase at constant surface pressure. The area increase could be quantitated and binding isotherms at different surface pressures were measured. A
M Laura Parnas et al.
American journal of clinical pathology, 135(2), 271-276 (2011-01-14)
Butyrylcholinesterase (BChE) metabolizes the paralytic succinylcholine. Extended paralysis occurs in people with inherited BChE variants that may be identified by measuring BChE activity with and without the inhibitor dibucaine to calculate a dibucaine number (DN). Accurate phenotyping requires phenotype-specific BChE
Jamie Nelsen et al.
Pediatric emergency care, 25(10), 670-673 (2009-10-17)
Dibucaine is considered one of the most potent and consequently toxic amide anesthetics available, and despite withdrawal from the US market as a spinal anesthetic, it remains accessible as an over-the-counter preparation in the United States. Dibucaine exposures in children
Thaïs Souto-Padrón et al.
Parasitology research, 99(4), 317-320 (2006-04-14)
Although local anesthetics (LA) are considered primarily Na+-channel blockers in the past decade, an alternative action of LA as inhibitors of fusion among compartments of the endocytic/exocytic pathways was described. In epimastigote forms of Trypanosoma cruzi, we observed that 50
Zhicheng Wang et al.
Archives of biochemistry and biophysics, 495(2), 136-143 (2010-01-12)
There are evidence that both a disintegrin and metalloproteinase 17 (ADAM17) and calpain are involved in platelet glycoprotein (GP)Ibalpha ectodomain cleavage. However, the relationship between the two enzymes in the shedding process remains unclear. Here we show that calcium ionophore

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