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Merck
모든 사진(1)

주요 문서

T116

Supelco

Thebaine

동의어(들):

Paramorphine

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About This Item

실험식(Hill 표기법):
C19H21NO3
CAS Number:
Molecular Weight:
311.37
EC Number:
MDL number:
UNSPSC 코드:
41116107

약물 제어

USDEA Schedule II; regulated under CDSA - not available from Sigma-Aldrich Canada

기술

HPLC: suitable
gas chromatography (GC): suitable

형식

neat

SMILES string

[H][C@@]12Oc3c(OC)ccc4C[C@H]5N(C)CC[C@]1(C5=CC=C2OC)c34

InChI

1S/C19H21NO3/c1-20-9-8-19-12-5-7-15(22-3)18(19)23-17-14(21-2)6-4-11(16(17)19)10-13(12)20/h4-7,13,18H,8-10H2,1-3H3/t13-,18+,19+/m1/s1

InChI key

FQXXSQDCDRQNQE-VMDGZTHMSA-N

유사한 제품을 찾으십니까? 방문 제품 비교 안내

애플리케이션

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

교체됨

제품 번호
설명
가격

픽토그램

Skull and crossbones

신호어

Danger

유해 및 위험 성명서

Hazard Classifications

Acute Tox. 3 Oral

Storage Class Code

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

WGK

WGK 3

Flash Point (°F)

Not applicable

Flash Point (°C)

Not applicable

개인 보호 장비

Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges


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시험 성적서(COA)

Lot/Batch Number

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이 제품을 이미 가지고 계십니까?

문서 라이브러리에서 최근에 구매한 제품에 대한 문서를 찾아보세요.

문서 라이브러리 방문

Xucong Lin et al.
Journal of separation science, 30(17), 3011-3017 (2007-10-27)
A method for the separation and determination of five major opium alkaloids (narcotine, papaverine, thebaine, codeine, and morphine) in pericarpium papaveris by pressurized CEC (pCEC) with monolithic column has been developed. Under the optimum condition, linear calibration ranges of narcotine
Gaik B Kok et al.
Organic & biomolecular chemistry, 9(4), 1008-1011 (2010-12-28)
Further investigations into the direct synthesis of N-nororipavine from oripavine using iron powder under non-classical Polonovski conditions have been conducted. The stoichiometry, solvents and iron oxidation rates were found to have a dramatic effect on the rate of N-demethylation as
Gilbert Stork et al.
Journal of the American Chemical Society, 131(32), 11402-11406 (2009-07-25)
Total syntheses of the morphine alkaloids are described that use a direct stereoselective formation of the phenanthrofuran system via an intramolecular 4 + 2 cycloaddition of a diene tethered to the 4-position of a 7-methoxybenzofuran-3-carboxylic acid ester.
Robert J Carroll et al.
The Journal of organic chemistry, 74(2), 747-752 (2008-12-17)
The ethylene glycol ketal of neopinone was prepared in a one-pot procedure by the reaction of thebaine with ethylene glyocol in the presence of p-toluenesulfonic acid. The ketal is also an intermediate in the conversion of thebaine to hydrocodone with
Ali A Ensafi et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 75(2), 867-871 (2010-01-01)
In this work, a batch chemiluminescence (CL) method has been proposed for the simultaneous determination of two structurally similar alkaloids, noscapine and thebaine. The method is based on the kinetic distinction of the CL reactions of noscapine and thebaine with

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