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左布比卡因

CAS 27262-47-1C18H28N2OMW 288.4

左布比卡因,CAS 登记号 27262-47-1,由济南圣和化工有限公司现货供应,可提供纯度 按批次COA提供(不公开发布) 的规格,下游主要用于有机化学品。支持样品与小批量试用,批量价格请联系我们获取,验收以批次 COA 为准。

规格参数

CAS号27262-47-1
分子式C18H28N2O
分子量288.4
LogP3.6
纯度按批次COA提供(不公开发布)
包装按订单/批次确认(不公开发布)
应用领域有机化学品
类别有机化学品

用途与场景

有机化学品

包装与供货

包装规格按订单/批次确认(不公开发布)
纯度规格按批次COA提供(不公开发布)
储存条件密封、阴凉干燥处保存
供货周期现货/按订单安排

文件与支持

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常见问题

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本页已列出 左布比卡因 的 CAS 号:27262-47-1,可与随货 COA 核对。

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左布比卡因 一般用在什么产品里?

主要涉及有机化学品。

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PubChem 公开数据

Description

Levobupivacaine · CAS 27262-47-1 · C18H28N2O. UNII A5H73K9U3W. Solubility: 9.77e-02 g/L; LogP: 3.6; Dissociation Constants: 8.1.

Identification

CAS Registry Number27262-47-1
PubChem CID92253
Molecular formulaC18H28N2O
IUPAC name(2S)-1-butyl-N-(2,6-dimethylphenyl)piperidine-2-carboxamide
UNII (FDA)A5H73K9U3W

Computed Descriptors

Molecular Weight288.4
XLogP33.4
Hydrogen Bond Donor Count1
Hydrogen Bond Acceptor Count2
Rotatable Bond Count5
Exact Mass288.220163521
Monoisotopic Mass288.220163521
Topological Polar Surface Area32.3
Heavy Atom Count21
Formal Charge0

Physical & Chemical Properties

Solubility9.77e-02 g/L
LogP3.6
Dissociation Constants8.1

Physical description & handling notes

  • Solid
  • Levobupivacaine, a local anesthetic agent, is indicated for the production of local or regional anesthesia or analgesia for surgery, for oral surgery procedures, for diagnostic and therapeutic procedures, and for obstetrical procedures.

GHS Hazard Classification

Reported hazard statementsH300, H310, H330 (33.3%), H301 (33.3%), H311 (33.3%), H370 (33.3%)

H300+H310+H330 (33.3%): Fatal if swallowed, in contact with skin or if inhaled [Danger Acute toxicity, oral; acute toxicity, dermal; acute toxicity, inhalation]

H300 (33.3%): Fatal if swallowed [Danger Acute toxicity, oral]

Documented Uses

  • For the production of local or regional anesthesia for surgery and obstetrics, and for post-operative pain management
  • Breast Feeding; Lactation; Anesthetics, Local
  • The plasma concentration of levobupivacaine following therapeutic administration depends on dose and also on route of administration, because absorption from the site of administration is affected by the vascularity of the tissue. Peak levels in blood were reached approximately 30 minutes after epidural administration, and doses up to 150 mg resulted in mean Cmax levels of up to 1.2 µg/mL.
  • Following intravenous administration, recovery of the radiolabelled dose of levobupivacaine was essentially quantitative with a mean total of about 95% being recovered in urine and feces in 48 hours. Of this 95%, about 71% was in urine while 24% was in feces.
  • 66.91 ±18.23 L [after intravenous administration of 40 mg in healthy volunteers]
  • 39.06 ±13.29 L/h [after intravenous administration of 40 mg in healthy volunteers]

Synonyms

Levobupivacaine; 27262-47-1; (S)-bupivacaine; (-)-bupivacaine; L-(-)-bupivacaine; (2S)-1-butyl-N-(2,6-dimethylphenyl)piperidine-2-carboxamide; Levobupivacaina; Novabupi; (S)-1-Butyl-2',6'-pipecoloxylidide; L-bupivacaine; Bupivacaine, (s)-; Bupivacaine, (-)-; L-(-)-1-Butyl-2',6'-pipecoloxylidide; A5H73K9U3W; CHEBI:6149; DTXSID8048496

Frequently Asked Questions

What are the CAS number and molecular formula of Levobupivacaine?

CAS 27262-47-1; molecular formula C18H28N2O; molecular weight — g/mol.

What other names is Levobupivacaine known by?

Levobupivacaine, 27262-47-1, (S)-bupivacaine, (-)-bupivacaine, L-(-)-bupivacaine, (2S)-1-butyl-N-(2,6-dimethylphenyl)piperidine-2-carboxamide.

Is Levobupivacaine classified as hazardous?

Hazard statements reported: H300, H310, H330, H301, H311.

What are the key physical properties of Levobupivacaine?

Solubility: 9.77e-02 g/L; LogP: 3.6; Dissociation Constants: 8.1.

Facts on this page are taken from PubChem (US National Library of Medicine) and Wikidata. Grade-specific data — assay, moisture, particle size, packaging, shelf life — is issued per batch on the COA and is not published here.

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