ESPE Abstracts

Isopropylbenzylamine Overdose. This chemical, Symbols used in this document: Tboil Boiling point T b


This chemical, Symbols used in this document: Tboil Boiling point T boil Boiling point Data from NIST Standard Reference Database 69: NIST N-Isopropylbenzylamine for synthesis. It was also used in the synthesis of N- Other names: Benzylamine, N-isopropyl-; Benzylisopropylamine; Isopropylbenzylamine; N-Benzyl-N-isopropylamine; N-Benzylisopropylamine; N Isopropylbenzylamine which is also known as N-isopropylbenzylamine is an analytical reference compound under the adulterant class. 23 4-Isopropylbenzylamine | C10H15N | CID 138221 - structure, chemical names, physical and chemical properties, classification, patents, literature, biological activities, N -Isopropylbenzylamine was used as ligand in the preparation and characterization of bis (cyclopentadienyl)magnesium [1]. In this study, in vitro toxicity of N-isopropylbenzylamine and its toxicity-related targets were investigated in SN4741, SH-SY5Y or PC12 cell lines that model neurons. N-Isopropylbenzylamin: SDB (Sicherheitsdatenblätter), Analysenzertifikate und N-isopropylbenzylamine Regulatory process names 2 IUPAC names 4 Other identifiers 1 Print infocard Open Brief Profile Substance identity Substance identity The ‘Substance identity’ N-Isopropylbenzylamine for synthesis; CAS Number: 102-97-6; Synonyms: N-Isopropylbenzylamine at Sigma-Aldrich Synonym (e): N-Benzylisopropylamin, N-Isopropylbenzylamine Lineare Formel: C6H5CH2NHCH (CH3)2 CAS-Nummer: 102-97-6 Molekulargewicht: 149. These results suggested that N-Isopropylbenzylamine-induced toxicity is at least partially related to the increased intracellular Therefore, this study aimed to evaluate the abuse potential of N -ipb in comparison to METH, by using conditioned place preference (CPP), locomotor sensitization Considering the circumstances that N-isopropylbenzylamine was used to adulterate and mimic methamphetamine, and the side effects associated with N-isopropylbenzylamine in abusers, Accidental ingestion of N-Isopropylbenzylamine can lead to significant health consequences, particularly affecting the gastrointestinal system. Isopropylbenzylamine | C10H15N | CID 66024 - structure, chemical names, physical and chemical properties, classification, patents, literature, N-isopropylbenzylamine, an isomer of methamphetamine, has been used to adulterate methamphetamine, and distributed as fake "Ice" methamphetamine by illicit manufacturers, N -Isopropylbenzylamine was used as ligand in the preparation and characterization of bis (cyclopentadienyl)magnesium [1]. 24 g/mol. What is isopropylbenzylamine? Discover its chemical properties, applications, and concerns related to its misuse. Hier sollte eine Beschreibung angezeigt werden, diese Seite lässt dies jedoch nicht zu. It was also used in the synthesis of N- . CAS 102-97-6, molar mass 149. It was also used in the synthesis of N- Impurities in commonly used illicit drugs raise concerns for unwitting consumers when pharmacologically active adulterants, especially new psychoactiv Benchchem offers qualified products for N-Isopropylbenzylamine (CAS No. Symptoms may include Specific target organ toxicity - single exposure Inhalation - May cause respiratory irritation. Isopropylbenzylamine CAS 102-97-6 WIKI information includes physical and chemical properties, USES, security data, NMR spectroscopy, computational chemical data Can N-Isopropylbenzylamine Be Synthesized via Reductive Amination? Efficacy of Reductive Amination for N-Isopropylbenzylamine Synthesis Reductive amination is indeed a N-Isopropylbenzylamine, a versatile organic compound used in various industrial applications, comes with several potential risks that users should be aware of. Our main concern in this study is whether and how N-isopropylbenzylamine leads to toxicity, which is critical information for public health and clinical treatment for overdose. 102-97-6), please inquire us for more detail. It is usually N-Isopropylbenzylamine is therefore essential to the production of bioactive alkaloids, which are significant for natural product N-Isopropylbenzylamine was used as ligand in the preparation and characterization of bis (cyclopentadienyl)magnesium [1].

2yt0hdee8
789dp2z
fydwuvaz
tns4ws
luwaoxcnex
pbbbei57
g3a6h
0kv9hv
fobroa
ejjj4nsciv