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依托芬那酯

CAS 30544-47-9C18H18F3NO4MW 369.3

济南圣和化工主营供应 依托芬那酯(CAS 30544-47-9),归类于有机化学品,分子式 C18H18F3NO4,分子量 369.3。我们面向国内化工贸易与生产企业提供稳定的现货供应,报价响应快,支持对公转账并可开具增值税发票。

产品概览

CAS号30544-47-9
分子式C18H18F3NO4
分子量369.3
LogP4.7
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

应用领域

有机化学品

依托芬那酯在有机化学品领域使用广泛。采购前请确认纯度等级与包装形式,以批次 COA 为验收依据。

包装与储存

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
运输常规化工运输
样品可协商提供
交期现货/按订单安排

供应说明:依托芬那酯 常规包装为按订单/批次确认(不公开发布),储存时应密封置于阴凉干燥处,避免与氧化剂混放。济南圣和化工有限公司 支持国内物流发货,大货交期与运费以订单确认为准。

质量与文件

每批产品随货提供 COA(分析证书);可按需提供 MSDS/技术数据表及第三方检测报告。纯度与包装以批次 COA 及订单确认为准。

关于供应商

选择 济南圣和化工有限公司 的理由:产品信息透明(含 CAS、分子式、理化参数)、报价响应快(一个工作日内)、单证齐全(COA/MSS/质检资料按需提供)、支持批量与长期协议供货。如需 依托芬那酯 以外的配套原料,也欢迎一并列出需求清单。

常见问题

依托芬那酯 的 CAS 号是多少?

依托芬那酯 的 CAS 号为 30544-47-9。

该产品的纯度和包装规格是什么?

常规纯度规格为 按批次COA提供(不公开发布),包装为 按订单/批次确认(不公开发布),随货提供 COA。

依托芬那酯 有什么用途?

主要应用于有机化学品。

如何购买或获取报价?

请发送邮件至 info@591daili.com 或通过 WhatsApp 联系,注明产品名称、CAS 号与需求数量,一个工作日内回复报价。供应商:济南圣和化工有限公司。

PubChem 公开数据

Description

Etofenamate · CAS 30544-47-9 · C18H18F3NO4. UNII KZF0XM66JC.

Identification

CAS Registry Number30544-47-9
PubChem CID35375
Molecular formulaC18H18F3NO4
IUPAC name2-(2-hydroxyethoxy)ethyl 2-[3-(trifluoromethyl)anilino]benzoate
UNII (FDA)KZF0XM66JC

Computed Descriptors

Molecular Weight369.3
XLogP34.7
Hydrogen Bond Donor Count2
Hydrogen Bond Acceptor Count8
Rotatable Bond Count9
Exact Mass369.11879254
Monoisotopic Mass369.11879254
Topological Polar Surface Area67.8
Heavy Atom Count26
Formal Charge0

GHS Hazard Classification

Reported hazard statementsH301 (100%), H400 (100%), H410 (100%)

H301 (100%): Toxic if swallowed [Danger Acute toxicity, oral]

H400 (100%): Very toxic to aquatic life [Warning Hazardous to the aquatic environment, acute hazard]

Documented Uses

  • Use (kg; approx.) in Germany (2009): >500
  • Consumption (g per capita; approx.) in Germany (2009): 0.00611
  • Anti-inflammatory agents that are non-steroidal in nature. In addition to anti-inflammatory actions, they have analgesic, antipyretic, and platelet-inhibitory actions. They act by blocking the synthesis of prostaglandins by inhibiting cyclooxygenase, which converts arachidonic acid to cyclic endoperoxides, precursors of prostaglandins. Inhibition of prostaglandin synthesis accounts for their analgesic, antipyretic, and platelet-inhibitory actions; other mechanisms may contribute to their anti-inflammatory effects.
  • M02 - Topical products for joint and muscular pain
  • M02A - Topical products for joint and muscular pain
  • M02AA - Antiinflammatory preparations, non-steroids for topical use

Synonyms

ETOFENAMATE; 30544-47-9; 2-(2-Hydroxyethoxy)ethyl 2-((3-(trifluoromethyl)phenyl)amino)benzoate; Etofenamato; Bay d 1107; Etofenamatum; TVX485; WHR-5020; DTXSID2045448; TVX-485; BAY-D-1107; KZF0XM66JC; BAYD-1107; 2-(2-hydroxyethoxy)ethyl 2-{[3-(trifluoromethyl)phenyl]amino}benzoate; Benzoic acid, 2-[[3-(trifluoromethyl)phenyl]amino]-, 2-(2-hydroxyethoxy)ethyl ester; 2-(2-Hydroxyethoxy)ethyl-N-(alpha,alpha,alpha-trifluoro-m-tolyl)anthranilate

Frequently Asked Questions

What are the CAS number and molecular formula of Etofenamate?

CAS 30544-47-9; molecular formula C18H18F3NO4; molecular weight — g/mol.

What other names is Etofenamate known by?

ETOFENAMATE, 30544-47-9, 2-(2-Hydroxyethoxy)ethyl 2-((3-(trifluoromethyl)phenyl)amino)benzoate, Etofenamato, Bay d 1107, Etofenamatum.

Is Etofenamate classified as hazardous?

Hazard statements reported: H301, H400, H410.

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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English page: Etofenamate

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