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Detail of "23964-58-1"

  • CAS Number:
  • 23964-58-1
  • Name:
  • 2-Thiophenecarboxylicacid, 4-methyl-3-[[1-oxo-2-(propylamino)propyl]amino]-, methyl ester

  • Superlist Name:
  • Articaine
  • Molecular Structure:
  • Formula:
  • C13H20N2O3S
  • Molecular Weight:
  • 284.37
  • Synonyms:
  • 2-Thiophenecarboxylicacid, 4-methyl-3-[2-(propylamino)propionamido]-, methyl ester (8CI);Carticaine;
  • Density:
  • 1.178 g/cm3
  • Boiling Point:
  • 440.6 °C at 760 mmHg
  • Flash Point:
  • 220.3 °C
  • Appearance:
  • White or white crystalline powder

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CAS No.23964-58-1 ArticaineCompetitive Product

Supplier:Wuhan Konberd Biotech Co., Ltd. [ China (Mainland)]

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CAS No.23964-58-1 Articaine

Assay:99%  Appearance:Powder  Package:25kg/drum

Supplier:HANGZHOU TOYOND BIOTECH CO., LTD [ China (Mainland)]

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CAS No.23964-58-1 Articaine

Assay:98%

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CAS No.23964-58-1 Articaine

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CAS No.23964-58-1 Articaine

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CAS No.23964-58-1 Articaine

Artecaine Hcl

Supplier:Hangzhou Starshine Pharmaceutical Co., LTD [ China (Mainland)]

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CAS No.23964-58-1 Articaine

Molecular Formula C13H20N2O3S Molecular Weight 284.37 CAS Registry Number 23964-58-1 It is a important intermediate of articaine HCl,for more details,please don't hesitate to contact us.

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CAS No.23964-58-1 Articaine

Neo-monobasic amides oral cavity local anesthetic, especially use to surgery course involving in osteosomy and mucous membrane incised, is only one used specially for oral cavity local anesthetic, which is supplied to domestic market. Usually it is prepared to the injection with

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CAS No.23964-58-1 Articaine

SPECIFICATION APPEARANCE:White or off-white crystalline powder ASSAY:≥98.5% MELTING POINT: 167~173℃ LOSS ON DRYING: ≤0. 5%

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Articaine Hydrochloride

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Articaine Hydrochloride

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ARTICAINE

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more information,please contact us

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Supplier:Ceres Chemical Co. Inc. [ United States]

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Supplier:shanxi top pharm chem [ China (Mainland)]

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Supplier:Shaanxi TOP Pharm Chemical Co., Ltd. [ China (Mainland)]

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CAS No.23964-58-1 Articaine

Supplier:RA Chem Pharma Limited [ India]

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Supplier:Shanghai Boyle Chemical Co.,Ltd [ China (Mainland)]

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Reference

In vitro studies on the effect of several local anesthetics on cell growth
In vitro studies on the effect of several local anesthetics on cell growth. Mechanisms of local side effects. Hack, G.; Karzel, K. (Anaesthesie Abt., Krankenhaus Singen, Singen D-7700, Fed. Rep. Ger.). Anaesthesiol. Intensivmed. (Berlin), 158(Neue Aspekte Regionalanaesth. 3), 94-103 (German) 1984. CODEN: ANIMD2. 94-24-6 and 137-58-6 which are cas registry numbers are also used here. ISSN: 0171-1814. DOCUMENT TYPE: Journal CA Section: 1 (Pharmacology) Toxic side effects of local anesthetics such as procaine [59-46-1], tetracaine [94-24-6], oxybuprocaine [99-43-4], lidocaine [137-58-6], mepivacaine [96-88-8], carticaine [23964-58-1], and bupivacaine [2180-92-9] were assessed by using an in vitro model (suspension culture of Ehrlich ascites tumor cells). All tested local anesthetics at clin. EDs inhibited cell growth; the most pronounced inhibiting effects were obsd. with oxybuprocaine, tetracaine, and bupivacaine. The growth inhibitory effect of procaine pointed to a colchicine-like effect in the metaphase, whereas the inhibitory effect of the remaining compds. appeared to be due to an interference in the interphase of these cells. The results were discussed in terms of the in vivo toxicity of these compds. used in clin. concns. .
On the interaction of local anesthetics with mast cells
On the interaction of local anesthetics with mast cells. Drabikova, K.; Nosal, R. (Centre Physiol. Sci., Slovak Acad. Sci., Bratislava 842 16, Czech.). Agents Actions, 20(3-4), 191-3 (English) 1987. CODEN: AGACBH. ISSN: 0065-4299.Several substances with their cas registry numbers 68931-03-3 and 50-36-2 may be metioned in this study. DOCUMENT TYPE: Journal CA Section: 1 (Pharmacology) The carbanilate local anesthetics carbisocaine [68931-03-3], heptacaine [55792-21-7], and pentacaine [104485-01-0] liberate histamine [51-45-6] from isolated rat mast cells. Procaine [59-46-1], carticaine [23964-58-1], trimecain [616-68-2], cocaine [50-36-2], and butanilicaine [3785-21-5] were ineffective. Histamine liberation was dose-dependent, followed by calcium displacement from membrane binding sites and occurred without concomitant degranulation. Low temp.- and pH-dependent inhibition of histamine liberation indicated a non-specific, membrane-perturbing effect of highly liposol. carbanilate local anesthetics. Conformational changes in the sodium channel on the mast cell membrane induced by carbanilate anesthetics might result in histamine exchange occurring intracellularly. .
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