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安全信息

Y0000453

Oxycodone impurity D

European Pharmacopoeia (EP) Reference Standard

别名:

14-Hydroxycodeinone, (5α)-7,8-Didehydro-4,5-epoxy-14-hydroxy-3-methoxy-17-methylmorphinan-6-one

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About This Item

经验公式(希尔记法):
C18H19NO4
CAS号:
分子量:
313.35
UNSPSC代码:
41116107
NACRES:
NA.24

等级

pharmaceutical primary standard

API类

oxycodone

制造商/商品名称

EDQM

药品控制

regulated under CDSA - not available from Sigma-Aldrich Canada

应用

pharmaceutical (small molecule)

格式

neat

储存温度

2-8°C

InChI

1S/C18H19NO4/c1-19-8-7-17-14-10-3-4-12(22-2)15(14)23-16(17)11(20)5-6-18(17,21)13(19)9-10/h3-6,13,16,21H,7-9H2,1-2H3/t13-,16?,17+,18-/m1/s1

InChI key

YYCRAERBSFHMPL-FSFXSCMFSA-N

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一般描述

This product is provided as delivered and specified by the issuing Pharmacopoeia. All information provided in support of this product, including SDS and any product information leaflets have been developed and issued under the Authority of the issuing Pharmacopoeia.For further information and support please go to the website of the issuing Pharmacopoeia.

应用

Oxycodone impurity D EP Reference standard, intended for use in laboratory tests only as specifically prescribed in the European Pharmacopoeia.

包装

The product is delivered as supplied by the issuing Pharmacopoeia. For the current unit quantity, please visit the EDQM reference substance catalogue.

其他说明

Sales restrictions may apply.

象形图

Skull and crossbonesHealth hazard

警示用语:

Danger

危险分类

Acute Tox. 2 Dermal - Acute Tox. 2 Inhalation - Acute Tox. 2 Oral - Muta. 1B

WGK

WGK 3

法规信息

监管及禁止进口产品

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分析证书(COA)

Lot/Batch Number

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A Szentesi et al.
Analytical and bioanalytical chemistry, 374(3), 427-431 (2002-10-10)
A negative Cotton effect is observed in the circular dichroism (CD) spectra of 6-oxo-morphinans in the wavelength range of n-pi* electron transitions. 6-oxo-Morphinans can be transformed into oxime derivatives with hydroxylamine and after oxime formation the CD spectra are significantly
D López et al.
The Journal of organic chemistry, 65(15), 4671-4678 (2000-08-26)
The photooxidation of thebaine (3) with a sun lamp affords two main products: hydrodibenzofuran 10 (major) and benzofuran 11 (minor). The latter compound becomes predominant if a Hg lamp is used instead of a sun lamp. The formation of 10
D L Lister et al.
FEMS microbiology letters, 181(1), 137-144 (1999-11-24)
A biotransformation mixture which contained codeine and washed cells of Pseudomonas putida M10 gave rise to a number of transformation products that are of clinical importance which included hydrocodone, dihydrocodeine and 14beta-hydroxycodeine. Incubations with the same organism and codeinone gave

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