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Merck
CN

36127

氯咪巴唑

PESTANAL®, analytical standard

别名:

1-(4-氯苯氧基)-1-(咪唑-1-基)-3,3-二甲基丁-2-酮

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关于此项目

经验公式(希尔记法):
C15H17ClN2O2
化学文摘社编号:
分子量:
292.76
UNSPSC Code:
41116107
NACRES:
NA.24
PubChem Substance ID:
EC Number:
253-775-4
Beilstein/REAXYS Number:
618020
MDL number:
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产品名称

氯咪巴唑, PESTANAL®, analytical standard

InChI key

OWEGWHBOCFMBLP-UHFFFAOYSA-N

InChI

1S/C15H17ClN2O2/c1-15(2,3)13(19)14(18-9-8-17-10-18)20-12-6-4-11(16)5-7-12/h4-10,14H,1-3H3

SMILES string

CC(C)(C)C(=O)C(Oc1ccc(Cl)cc1)n2ccnc2

grade

analytical standard

product line

PESTANAL®

shelf life

limited shelf life, expiry date on the label

technique(s)

HPLC: suitable
NMR: suitable
gas chromatography (GC): suitable

mp

96-100 °C

suitability

passes test for identity (NMR)

application(s)

agriculture
environmental

format

neat

Quality Level

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Application

有关合适的仪器技术的更多信息,请参阅产品′的检验报告。想要获得更多支持,请联系技术服务部。
此氯咪巴唑可作为参考标准品,用于通过超高效液相色谱-串联质谱(UHPLC-MS-MS)测定环境样品和去屑洗发水样品中的氯咪巴唑。

General description

氯咪巴唑(Climbazole)是咪唑类抗真菌剂,由于可抑制微生物生长和保护头皮屏障而广泛用作抗头屑(AD)洗发水的活性成分。

Other Notes

请在我们的在线平台NMR用请在我们的在线平台NMR用ChemisTwin®查找本产品的数字化标准物质。您可以利用ChemisTwin®上的数字化等效物质进行样品确认和化合物定量(采用数字化外标)。您可以查看该物质的NMR 谱,点击鼠标即可与您的样品在线比较。点击此处了解更多信息,并开始免费试用

Legal Information

PESTANAL is a registered trademark of Merck KGaA, Darmstadt, Germany

pictograms

Exclamation markEnvironment

signalword

Warning

hcodes

Hazard Classifications

Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1

存储类别

13 - Non Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Faceshields, Gloves


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Yan-Wei Yang et al.
Wei sheng yan jiu = Journal of hygiene research, 34(5), 626-628 (2005-12-07)
A high performance liquid chromatography method was established for determination of antidangdruff agent salicylic acid,zinc pyrithione, octopirox, climbazole and ketoconazole in shampoo on a C18 column using acetonitrile-metholaqueous solution (10 mmol/L KH2 PO4 and 5 mmol/L EDTANa2, pH is adjusted
Yasuna Kobayashi et al.
Biological & pharmaceutical bulletin, 25(1), 53-57 (2002-02-05)
To determine the effect of climbazole on hepatic microsomal cytochrome P450 (P450) and drug-metabolizing enzymes, four different P450 isoforms (CYP2B1, 3A2, 2E1, and 2C12) were examined in female Long-Evans rats. Treatment of rats with climbazole resulted in the induction of
Y Kobayashi et al.
The Journal of toxicological sciences, 26(3), 141-150 (2001-09-13)
We examined the effect of climbazole on the induction of rat hepatic microsomal cytochrome P450 (P450), and compared the induction potency with other N-substituted azole drugs such as clorimazole. We found that climbazole is found to be a potent inducer
C Coiffard et al.
Annales pharmaceutiques francaises, 57(5), 392-396 (1999-10-16)
We compared thermostability of various natural (sulfoprolamine and sodium usnate) or synthetic (climbazol and piroctone olamine) antidandruff agents in aqueous diluted solution at pH around 7. Thermodegradation of these solutions was studied by an isothermal method in thermostatically controlled ovens
Alex A Pérez-Rivera et al.
Mutation research, 672(1), 27-39 (2008-10-28)
Climbazole is an imidazole antifungal agent that can provide anti-dandruff benefits when incorporated into a shampoo matrix. A series of genotoxicity studies were performed to support the human safety of this azole antifungal drug. Climbazole was not mutagenic in the

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