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Y101

Supelco

YS-035 hydrochloride

analytical standard, for drug analysis

Synonym(s):

N-(-2-[3,4-Dimethoxyphenyl]ethyl)-3,4-dimethoxy-N-methylbenzeneethanamine

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About This Item

Empirical Formula (Hill Notation):
C21H29NO4 · HCl
CAS Number:
Molecular Weight:
395.92
MDL number:
UNSPSC Code:
41116107
PubChem Substance ID:
NACRES:
NA.24

grade

analytical standard, for drug analysis

Quality Level

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

application(s)

forensics and toxicology
pharmaceutical (small molecule)
veterinary

format

neat

SMILES string

Cl[H].COc1ccc(CCN(C)CCc2ccc(OC)c(OC)c2)cc1OC

InChI

1S/C21H29NO4.ClH/c1-22(12-10-16-6-8-18(23-2)20(14-16)25-4)13-11-17-7-9-19(24-3)21(15-17)26-5;/h6-9,14-15H,10-13H2,1-5H3;1H

InChI key

GYBONEHHSUABAO-UHFFFAOYSA-N

Application

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

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

JAN Code

Y101-50MG:
Y101-BULK:
Y101-10MG:
Y101-VAR:


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R Deana et al.
The Biochemical journal, 218(3), 899-905 (1984-03-15)
Compound YS 035 [NN-bis-(3,4-dimethoxyphenethyl)-N-methylamine] is a new synthetic compound capable of inhibiting Ca2+ uptake by different cells. The inhibition of Ca2+ uptake by muscle cells isolated from chicken embryo is dose-dependent in the compound YS 035 concentration range 10-30 microM.
S L Mironov et al.
The European journal of neuroscience, 12(2), 520-526 (2000-03-11)
A hyperpolarization-activated current, Ih, is often implied in pacemaker-like depolarizations during rhythmic oscillatory activity. We describe Ih in the isolated respiratory centre of immature mice (P6-P11). Ih was recorded in 15% (22/146) of all inspiratory neurons examined. The mean half-maximal
P C Levesque et al.
Toxicology and applied pharmacology, 94(1), 55-65 (1988-06-15)
Agents known to disrupt intraterminal Ca2+ buffering, N,N-dimethylamino-8-octyl-3,4,5-trimethoxybenzoate (TMB-8), 25 microM; caffeine, 7.5 mM; N,N-bis(3,4-dimethoxyphenethyl)-N-methylamine (YS035), 180 microM; ouabain, 200 microM; and dantrolene, 50 microM, were tested for the ability to alter effects of methyl mercury (MeHg) on spontaneous quantal
F Berger et al.
Naunyn-Schmiedeberg's archives of pharmacology, 344(6), 653-661 (1991-12-01)
The electrophysiologic mode of action and potency of the verapamil derivative YS 035 (N,N-bis-(3,4-dimethoxyphenethyl)-N-methyl amine) were investigated in sheep cardiac Purkinje fibres. Action potential duration measured at a repolarization level of -60 mV (APD-60) and membrane currents recorded with the
Carbamazepine and L-type calcium channel inhibitors: a binding assay study.
E T Ngan et al.
Biological psychiatry, 39(11), 979-981 (1996-06-01)

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