M-012
(±)-MDA solution
1.0 mg/mL in methanol, ampule of 1 mL, certified reference material, Cerilliant®
동의어(들):
(±)-3,4-Methylenedioxyamphetamine
로그인조직 및 계약 가격 보기
모든 사진(1)
About This Item
실험식(Hill 표기법):
C10H13NO2
CAS Number:
Molecular Weight:
179.22
MDL number:
UNSPSC 코드:
41116107
PubChem Substance ID:
NACRES:
NA.24
추천 제품
Grade
certified reference material
Quality Level
형태
liquid
특징
Snap-N-Spike®/Snap-N-Shoot®
포장
ampule of 1 mL
제조업체/상표
Cerilliant®
drug control
Narcotic Licence Schedule D (Switzerland); psicótropo (Spain); Decreto Lei 15/93: Tabela IIA (Portugal)
농도
1.0 mg/mL in methanol
기술
gas chromatography (GC): suitable
liquid chromatography (LC): suitable
응용 분야
forensics and toxicology
형식
single component solution
저장 온도
−20°C
SMILES string
NC(C)CC1=CC=C(OCO2)C2=C1
InChI
1S/C10H13NO2/c1-7(11)4-8-2-3-9-10(5-8)13-6-12-9/h2-3,5,7H,4,6,11H2,1H3
InChI key
NGBBVGZWCFBOGO-UHFFFAOYSA-N
일반 설명
A certified solution standard suitable to use in LC/MS or GC/MS applications for clinical toxicology, forensic analysis, or urine drug testing. MDA, or 3,4-methylenedioxyamphetamine, is an illicit recreational drug of the amphetamine and phenethylamine classes. Also known as tenamphetamine, MDA is abused for its psychedelic and hallucinogenic effects, similar to those of MDMA (Ecstasy).
애플리케이션
- MDA Research Chemical: (±)-MDA solution is extensively used in scientific research to study its pharmacological properties, including its effects on neurotransmitter systems which are critical in understanding substance-related disorders.
- MDA Enantiomers: The solution includes both enantiomers of MDA, allowing for detailed studies on the differential biological activities of each enantiomer in neuropharmacological research.
- Synthetic MDA Solution: This synthetic solution is crucial for controlled studies in biochemistry and pharmacology, providing a consistent baseline for experimental reproducibility and validation.
- MDA Biochemistry Application: Utilized in biochemical assays, (±)-MDA solution helps in the exploration of its metabolic pathways and interactions with biological macromolecules, enhancing the understanding of its pharmacodynamics.
- MDA Pharmacological Studies: As a key tool in pharmacological research, (±)-MDA solution is used to investigate its potential therapeutic effects and risks, contributing to the development of safety guidelines and therapeutic protocols.
법적 정보
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
관련 제품
제품 번호
설명
가격
신호어
Danger
유해 및 위험 성명서
Hazard Classifications
Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Flam. Liq. 2 - STOT SE 1
표적 기관
Eyes
Storage Class Code
3 - Flammable liquids
WGK
WGK 1
Flash Point (°F)
49.5 °F - closed cup
Flash Point (°C)
9.7 °C - closed cup
시험 성적서(COA)
제품의 로트/배치 번호를 입력하여 시험 성적서(COA)을 검색하십시오. 로트 및 배치 번호는 제품 라벨에 있는 ‘로트’ 또는 ‘배치’라는 용어 뒤에서 찾을 수 있습니다.
Raul López-Arnau et al.
British journal of pharmacology, 167(2), 407-420 (2012-04-19)
Here, we have compared the neurochemical profile of three new cathinones, butylone, mephedrone and methylone, in terms of their potential to inhibit plasmalemmal and vesicular monoamine transporters. Their interaction with 5-HT and dopamine receptors and their psychostimulant effect was also
Camilla Montesano et al.
Journal of mass spectrometry : JMS, 48(1), 49-59 (2013-01-11)
This study describes a method for the screening of methylenedioxyamphetamine- and piperazine-derived compounds in urine by liquid chromatography-tandem mass spectrometry. These substances, characterized by possessing common moieties, are screened using precursor ion and neutral loss scan mode and then quantified
M Barenys et al.
Reproductive toxicology (Elmsford, N.Y.), 34(1), 57-65 (2012-03-07)
MDMA consumers are young people of childbearing age. Consequently, developmental exposure to this drug is a potential public health concern. Several studies have addressed MDMA neurotoxicity in adults; however, knowledge of the effects of MDMA on developing embryos is limited.
Keiko Nakanishi et al.
Analytical and bioanalytical chemistry, 404(8), 2427-2435 (2012-09-27)
A liquid chromatography-electrospray ionization tandem mass spectrometry (LC-ESI-MS/MS) procedure was developed for the simultaneous determination of enantiomers of the prevalent designer drug 3,4-methylenedioxymethamphetamine (MDMA) and its phase I and phase II metabolites in urine with chiral derivatization. The analytes in
Han-yi Zhu et al.
Nan fang yi ke da xue xue bao = Journal of Southern Medical University, 31(11), 1858-1862 (2011-12-01)
To investigate the effect of piperphentonamine hydrochloride (PPTA) on cognitive deficits induced by ischemia-reperfusion and explore the possible mechanisms. SD rats were randomly divided into sham-operated group, ischemia-reperfusion group (with saline injection), PPTA-treated groups (2.5, 5, 10 mg/kg) and edaravone-treated
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