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Merck

P9879

Procaine hydrochloride

≥97% (HPLC), powder, Na⁺ channel blocker

Synonyme(s) :

Ester 2-diéthylaminoéthyl d’acide 4-aminobenzoïque, Ester diéthylaminoéthyl d’acide p-aminobenzoïque hydrochloride, Novocaïne hydrochloride

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A propos de cet article

Formule linéaire :
H2NC6H4CO2CH2CH2N(C2H5)2·HCl
Numéro CAS:
Poids moléculaire :
272.77
NACRES:
NA.77
PubChem Substance ID:
UNSPSC Code:
12352200
EC Number:
200-077-2
MDL number:
Beilstein/REAXYS Number:
3917802

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Nom du produit

Procaine hydrochloride, ≥97%

InChI key

HCBIBCJNVBAKAB-UHFFFAOYSA-N

InChI

1S/C13H20N2O2.ClH/c1-3-15(4-2)9-10-17-13(16)11-5-7-12(14)8-6-11;/h5-8H,3-4,9-10,14H2,1-2H3;1H

SMILES string

Cl.CCN(CC)CCOC(=O)c1ccc(N)cc1

assay

≥97%

form

powder

mp

155-156 °C (lit.)

originator

Celgene

Quality Level

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Cet article
1564006P31000001561008
form

powder

form

-

form

-

form

-

assay

≥97%

assay

-

assay

-

assay

-

Quality Level

200

Quality Level

-

Quality Level

-

Quality Level

-

originator

Celgene

originator

-

originator

-

originator

-

mp

155-156 °C (lit.)

mp

155-156 °C (lit.)

mp

155-156 °C (lit.)

mp

-

Gene Information

human ... SCN10A(6336), SCN11A(11280), SCN1A(6323), SCN2A(6326), SCN3A(6328), SCN4A(6329), SCN5A(6331), SCN7A(6332), SCN8A(6334), SCN9A(6335)

Gene Information

human ... SCN10A(6336), SCN11A(11280), SCN1A(6323), SCN2A(6326), SCN3A(6328), SCN4A(6329), SCN5A(6331), SCN7A(6332), SCN8A(6334), SCN9A(6335)

Gene Information

human ... SCN10A(6336), SCN11A(11280), SCN1A(6323), SCN2A(6326), SCN3A(6328), SCN4A(6329), SCN5A(6331), SCN7A(6332), SCN8A(6334), SCN9A(6335)

Gene Information

human ... SCN10A(6336), SCN11A(11280), SCN1A(6323), SCN2A(6326), SCN3A(6328), SCN4A(6329), SCN5A(6331), SCN7A(6332), SCN8A(6334), SCN9A(6335)

Application

Procaine hydrochloride has been used as a component of Krebs Henseleit buffer for incubating the left ventricular cardiac tissue in its resting length.[1] It has also been used as an inducer in M9 media for induction assay.[2]

Biochem/physiol Actions

Procaine is a Na+ channel blocker, commonly used as an anesthetic agent and is considered safer than cocaine.[3] It is also useful as a painkiller to treat pain, associated with joints and tendons.[4]

Features and Benefits

This compound is a featured product for Gene Regulation research. Click here to discover more featured Gene Regulation products. Learn more about bioactive small molecules for other areas of research at sigma.com/discover-bsm.
This compound was developed by Celgene. To browse the list of other pharma-developed compounds and Approved Drugs/Drug Candidates, click here.

pictograms

Skull and crossbones

signalword

Danger

hcodes

Hazard Classifications

Acute Tox. 3 Oral - Skin Sens. 1

Classe de stockage

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges


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Consulter la Bibliothèque de documents

Characterization of combinatorial patterns generated by multiple two-component sensors in E. coli that respond to many stimuli
Clarke EJ and Voigt CA
Biotechnology and Bioengineering, 108(3), 666-675 (2011)
Phillippe P Gonzalez et al.
Glia, 66(5), 999-1015 (2018-02-03)
Malignant glioma is one of the deadliest types of cancer. Understanding how the cell of origin progressively evolves toward malignancy in greater detail could provide mechanistic insights and lead to novel concepts for tumor prevention and therapy. Previously we have
J Dudel et al.
Journal of neurophysiology, 81(5), 2386-2397 (1999-05-13)
of quantal end-plate currents of mouse muscle by physostigmine and procaine. Quantal endplate currents (qEPCs) were recorded from hemidiaphragms of mice by means of a macro-patch-clamp electrode. Excitation was blocked with tetrodotoxin, and quantal release was elicited by depolarizing pulses
Equine Anesthesia E-Book: Monitoring and Emergency Therapy, 215-215 (2002)
Ophthalmic Anaesthesia, 5-5 (2002)

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