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73360-54-0

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  • 2-Piperidinecarboxamide, 1-butyl-N-(2,6-dimethylphenyl)-, monohydrochloride, monohydrate

    Cas No: 73360-54-0

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73360-54-0 Usage

Description

Bupivacaine Hydrochloride is a synthetic amino amide local anesthetic with both hydrophilic and lipophilic properties. It is a Na+ channel blocker, cAMP production inhibitor, adrenergic antagonist, and an inhibitor of cholinesterase (EC 3.1.1.8) and Ca(2+)-transporting ATPase (EC 3.6.3.8). Its unique properties make it a versatile compound for various applications.

Uses

Used in Medical Industry:
Bupivacaine Hydrochloride is used as a local anesthetic for providing pain relief during surgical procedures and other medical interventions. It acts by blocking the Na+ channels, preventing the transmission of nerve impulses and thus inducing local anesthesia.
Used in Pharmaceutical Industry:
Bupivacaine Hydrochloride is used as a cAMP production inhibitor, which can help regulate cellular processes and signaling pathways. This property makes it useful in the development of drugs targeting specific cellular mechanisms.
Used in Cosmetic Industry:
As a surfactant molecule with both hydrophilic and lipophilic properties, Bupivacaine Hydrochloride can be used in the formulation of cosmetic products to improve their stability, texture, and performance.
Used in Research Applications:
Bupivacaine Hydrochloride is used as an adrenergic antagonist, cholinesterase inhibitor, and Ca(2+)-transporting ATPase inhibitor in various research applications. These properties make it a valuable tool for studying the mechanisms of action of different biological processes and the development of new therapeutic agents.

Check Digit Verification of cas no

The CAS Registry Mumber 73360-54-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,3,3,6 and 0 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 73360-54:
(7*7)+(6*3)+(5*3)+(4*6)+(3*0)+(2*5)+(1*4)=120
120 % 10 = 0
So 73360-54-0 is a valid CAS Registry Number.

73360-54-0 Well-known Company Product Price

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  • (1078507)  Bupivacaine hydrochloride  United States Pharmacopeia (USP) Reference Standard

  • 73360-54-0

  • 1078507-300MG

  • 4,339.53CNY

  • Detail
  • Sigma-Aldrich

  • (B5274)  Bupivacainehydrochloridemonohydrate  analytical standard, for drug analysis

  • 73360-54-0

  • B5274-1G

  • 875.16CNY

  • Detail
  • Sigma-Aldrich

  • (B5274)  Bupivacainehydrochloridemonohydrate  analytical standard, for drug analysis

  • 73360-54-0

  • B5274-5G

  • 1,471.86CNY

  • Detail
  • Sigma-Aldrich

  • (B5274)  Bupivacainehydrochloridemonohydrate  analytical standard, for drug analysis

  • 73360-54-0

  • B5274-15G

  • 3,347.37CNY

  • Detail

73360-54-0SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name bupivacaine hydrochloride hydrate

1.2 Other means of identification

Product number -
Other names Win 11,318

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:73360-54-0 SDS

73360-54-0Upstream product

73360-54-0Downstream Products

73360-54-0Relevant articles and documents

Biocompatible crosslinked hydrogels, drug-loaded hydrogels and methods of using the same

-

, (2015/09/28)

Disclosed are hydrogel compositions formed by the mixture of a tetramethylmethane substituted with one or more polyethylene glycols, and wherein each polyethylene glycol substituent is independently further substituted with one or more electrophilic groups, and a tetramethylmethane substituted with one or more polyethylene glycols, and wherein each polyethylene glycol substituent is independently further substituted with one or more nucleophilic groups. Disclosed are also methods of preparing the above hydrogels. The hydrogel compositions can further comprise pharmaceuticals, such as analgesics or local anesthetics. Disclosed are also methods of sealing a wound, preventing post-surgical adhesion, and reducing post-surgical pain using the disclosed hydrogels.

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