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Merck
CN

M-013

3,4-亚甲基二氧基甲基苯丙胺标准液(MDMA) 溶液

1.0 mg/mL in methanol, ampule of 1 mL, certified reference material, Cerilliant®

别名:

(±)-3,4-亚甲二氧基甲基苯异丙胺

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关于此项目

经验公式(希尔记法):
C11H15NO2
化学文摘社编号:
分子量:
193.24
NACRES:
NA.24
PubChem Substance ID:
UNSPSC Code:
41116107
EC Number:
200-659-6
MDL number:
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产品名称

3,4-亚甲基二氧基甲基苯丙胺标准液(MDMA) 溶液, 1.0 mg/mL in methanol, ampule of 1 mL, certified reference material, Cerilliant®

InChI key

SHXWCVYOXRDMCX-UHFFFAOYSA-N

InChI

1S/C11H15NO2/c1-8(12-2)5-9-3-4-10-11(6-9)14-7-13-10/h3-4,6,8,12H,5,7H2,1-2H3

SMILES string

CC(CC1=CC=C(OCO2)C2=C1)NC

grade

certified reference material

form

liquid

feature

Snap-N-Spike®/Snap-N-Shoot®

packaging

ampule of 1 mL

manufacturer/tradename

Cerilliant®

drug control

Narcotic Licence Schedule D (Switzerland); psicótropo (Spain); Decreto Lei 15/93: Tabela IIA (Portugal); Pszichotróp anyag / Psychotropic Substance (Hungary), 78/2022. (XII. 28.) BM rendelet
kontrollierte Droge in Deutschland

Quality Level

concentration

1.0 mg/mL in methanol

technique(s)

gas chromatography (GC): suitable
liquid chromatography (LC): suitable

application(s)

forensics and toxicology

format

single component solution

storage temp.

−20°C

Legal Information

German
Dieses Produkt fällt unter das Betäubungsmittelgesetz (BtMG). Für eine Bestellung dieses Produktes ist eine Erlaubnis nach § 3 BtMG zwingend erforderlich, es sei denn, es greift eine Ausnahme von der Erlaubnispflicht nach § 4 oder § 26 BtMG.

English
This product is subject to the German Narcotics Act. A permit under Section 3 of the German Narcotics Act is mandatory for ordering this product unless an exemption from the permit requirement under Section 4 or Section 26 of the German Narcotics Act applies.
CERILLIANT is a registered trademark of Merck KGaA, Darmstadt, Germany
Snap-N-Shoot is a registered trademark of Cerilliant Corporation
Snap-N-Spike is a registered trademark of Merck KGaA, Darmstadt, Germany

Application

该认证标准物质(CRM)还可作如下用途:
  • 使用基于铂纳米颗粒(沉积于碳纳米角上)的敏感传感器对人血清和尿液中的吗啡和 MDMA 进行电化学检测
  • 通过液相色谱-串联质谱(MS/MS)和二极管阵列检测器(DAD)两种方法对查获毒品安非他明、甲基苯丙胺和 MDMA 进行对映体评估
  • 建立和验证立体选择液相色谱-串联质谱(LC-MS/MS)方法以便分析人血浆样品中的 MDMA 及其代谢物
  • 基于基质辅助激光解吸/电离三重四极杆串联质谱法(MALDI-QqQ-MS/MS)分析口服液中 MDMA 及其代谢物 3,4-亚甲基二氧安非他明
  • 使用掺硼金刚石电极(BDDE)通过差分脉冲伏安法(DPV)鉴定和定量测定查获毒品样品中的 MDMA

Features and Benefits

  • 完全符合 ISO/IEC 17025 和 ISO 17034 认证
  • 附综合分析证书(CoA),包括稳定性、均匀性、浓度准确性、不确定性和可追溯性数据
  • 通过实时稳定性研究严格测试,以确保准确性和保质期
  • 使用合格的精密天平进行重量准备,以确保最小不确定性
  • 氩气环境下火焰密封,装入安瓿以便长期保存
  • 提供方便的 DEA 豁免格式,以提高实验室效率

General description

一种认证的 Snap-N-Spike® 溶液,适合作为校准物或对照品中的起始材料用于从法医分析和临床毒理学到尿液药物检测的各种 LC/MS 或 GC/MS 应用。

(±)-3,4-亚甲基二氧基甲基苯丙胺(MDMA)属于外消旋苯丙胺类兴奋剂。它具有精神活性,是合成致幻剂摇头丸的有效成分。MDMA 是一种非法药物,具有多种街道名称,如“迷幻药”、“E”、“X”和“XTC”。MDMA 是苯乙胺和苯丙胺类的类似物,因其心情愉快症作用和迷幻效果而被滥用。

Other Notes

在我们的NMR在线平台ChemisTwin®上可以找到本品对应的数字化标准物质。您可使用ChemisTwin®上的数字等效品鉴定您的样品并进行定量分析(使用数字化外标)。可查看该物质的NMR谱图,只需点击几次鼠标,就能进行在线样品比对。欢迎点击了解更多,开启免费试用之旅。

signalword

Danger

Hazard Classifications

Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Flam. Liq. 2 - STOT SE 1

target_organs

Eyes,Central nervous system

存储类别

3 - Flammable liquids

wgk

WGK 2

flash_point_f

49.5 °F - closed cup

flash_point_c

9.7 °C - closed cup

法规信息

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Typical scenarios of drug-facilitated sexual assaults usually involve victims having ingested a drink after which they had little, partial or no recollection of events for a period of time. We were surprised by the case of a woman who was
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The Climate Schools: Ecstasy module is a universal harm-minimisation school-based prevention program for adolescents aged 14 to 16 years. The program was developed to address the need for Ecstasy prevention given the increasing use of Ecstasy use among young Australians.
Stanley C Flavel et al.
PloS one, 7(12), e52025-e52025 (2012-12-29)
Use of illicit stimulants such as methamphetamine, cocaine, and ecstasy is a significant health problem. The United Nations Office on Drugs and Crime estimates that 14-57 million people use stimulants each year. Chronic use of illicit stimulants can cause neurotoxicity
Re: "Spice, bath salts, and the U.S. Military: the emergence of synthetic cannabinoid receptor agonists and cathinones in the U.S. Armed Forces".
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