环吡酮胺

Name: 环吡酮胺
Brand: 济南圣和化工有限公司

CAS 41621-49-2C14H24N2O3MW 268.35

环吡酮胺，CAS 登记号 41621-49-2，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41621-49-2

分子式C14H24N2O3

分子量268.35

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

在哪里能查到环吡酮胺的 CAS 号？

本页已列出环吡酮胺的 CAS 号：41621-49-2，可与随货 COA 核对。

可以提供哪些规格和包装？

常见纯度为按批次COA提供(不公开发布)，包装形式为按订单/批次确认(不公开发布)，特殊规格可在询价时说明。

环吡酮胺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

ciclopirox olamine · CAS 41621-49-2 · C14H24N2O3. UNII 50MD4SB4AP.

Identification

CAS Registry Number	41621-49-2
PubChem CID	38911
Molecular formula	C14H24N2O3
IUPAC name	2-aminoethanol;6-cyclohexyl-1-hydroxy-4-methylpyridin-2-one
UNII (FDA)	50MD4SB4AP

Computed Descriptors

Molecular Weight	268.35
Hydrogen Bond Donor Count	3
Hydrogen Bond Acceptor Count	4
Rotatable Bond Count	2
Exact Mass	268.17869263
Monoisotopic Mass	268.17869263
Topological Polar Surface Area	86.8
Heavy Atom Count	19
Formal Charge	0
Complexity	335

Regulatory Status

Regulatory & Food Contact	CIR / INCI: Antidandruff; Antimicrobial
GHS notification summary	0.9% (1 / 112)

GHS Hazard Classification

GHS notification summary	0.9% (1 / 112)
Reported hazard statements	H315 (43.8%), H317 (10.7%), H319 (42.9%), H335 (42%), H400 (56.2%)

This chemical does not meet GHS hazard criteria for 0.9% (1 of 112) of reports.

H315 (43.8%): Causes skin irritation [Warning Skin corrosion/irritation]

Documented Uses

Used as a topical treatment in immunocompetent patients with mild to moderate onychomycosis of fingernails and toenails without lunula involvement, due to <i>Trichophyton rubrum</i>.
Cosmetics -> Antidandruff; Antimicrobial
Substances that destroy fungi by suppressing their ability to grow or reproduce. They differ from FUNGICIDES, INDUSTRIAL because they defend against fungi present in human or animal tissues.
Decreased Protein Synthesis [PE]; Decreased RNA Replication [PE]; Decreased DNA Replication [PE]; Protein Synthesis Inhibitors [MoA]
Glucuronidation is the main metabolic pathway of ciclopirox. Route of Elimination: Most of the compound is excreted either unchanged or as glucuronide. After oral administration of 10 mg of radiolabeled drug (14C-ciclopirox) to healthy volunteers, approximately 96% of the radioactivity was excreted renally within 12 hours of administration. Ninety-four percent of the renally excreted radioactivity was in the form of glucuronides. Half Life: 1.7 hours for 1% topical solution.

Synonyms

Ciclopirox olamine; 41621-49-2; Batrafen; Micoxolamina; Brumixol; Mycoster; Ciclochem; Dafnegin; HOE 296; Ciclopirox ethanolamine salt (1:1); DTXSID6045583; HOE-296; 50MD4SB4AP; NSC-336278; DTXCID4025583; cyclopyroxolamine

Frequently Asked Questions

What are the CAS number and molecular formula of ciclopirox olamine?

CAS 41621-49-2; molecular formula C14H24N2O3; molecular weight — g/mol.

What other names is ciclopirox olamine known by?

Ciclopirox olamine, 41621-49-2, Batrafen, Micoxolamina, Brumixol, Mycoster.

What is the regulatory status of ciclopirox olamine?

Documented regulatory listings: CIR / INCI: Antidandruff; Antimicrobial.

Is ciclopirox olamine classified as hazardous?

0.9% of GHS notifications report no hazard classification (1 of 112).

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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