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Merck
CN

P9422

普莫卡因 盐酸盐

analytical standard, ≥98%

别名:

4-[3-(4-Butoxyphenoxy)propyl]morpholine hydrochloride

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关于此项目

经验公式(希尔记法):
C17H27NO3 · HCl
化学文摘社编号:
分子量:
329.86
NACRES:
NA.24
PubChem Substance ID:
UNSPSC Code:
41116107
EC Number:
211-293-1
MDL number:
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InChI key

SYCBXBCPLUFJID-UHFFFAOYSA-N

InChI

1S/C17H27NO3.ClH/c1-2-3-12-20-16-5-7-17(8-6-16)21-13-4-9-18-10-14-19-15-11-18;/h5-8H,2-4,9-15H2,1H3;1H

SMILES string

Cl.CCCCOc1ccc(OCCCN2CCOCC2)cc1

grade

analytical standard

assay

≥98%

technique(s)

HPLC: suitable, gas chromatography (GC): suitable

application(s)

forensics and toxicology
pharmaceutical (small molecule)

format

neat

Quality Level

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General description

Pramoxine hydrochloride is a surface and local anesthetic agent , which provides relief from itching and pain for a short period of time.

Application

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Biochem/physiol Actions

用于皮肤或粘膜的局部麻醉

pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

存储类别

11 - Combustible Solids

wgk

WGK 3

ppe

dust mask type N95 (US), Eyeshields, Gloves


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Rapid high-performance liquid chromatographic determination of pramoxine hydrochloride in topical cream and suppositories.
Z L Chang et al.
Journal of chromatography, 291, 428-433 (1984-05-18)
Allergy to pramoxine (pramocaine).
W G van Ketel
Contact dermatitis, 7(1), 49-49 (1981-01-01)
Uncovering tinea incognito. Topical corticosteroids can mask typical features of ringworm.
Carrie A Oklota et al.
Postgraduate medicine, 116(1), 65-66 (2004-07-28)
Canine and Feline Dermatology Drug Handbook (2012)
R Weinberger et al.
Journal of pharmaceutical sciences, 69(4), 475-477 (1980-04-01)
A rapid and quantitative method for the determination of pramoxine hydrochloride by high-pressure liquid chromatography is presented. The drug is extracted as the salt from a preparation with a high lipoid composition by partitioning it to the aqueous phase of

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