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D204

Sigma-Aldrich

S-(+)-O-Desmethylraclopride hydrobromide

solid, ≥98% (HPLC)

Synonym(s):

(S)-3,5-Dichloro-N-[(1-ethyl-2-pyrrolidinyl)methyl]-2,6-dihydroxybenzamide hydrobromide

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About This Item

Empirical Formula (Hill Notation):
C14H18Cl2N2O3 · HBr
CAS Number:
Molecular Weight:
414.12
MDL number:
UNSPSC Code:
12352202
PubChem Substance ID:
NACRES:
NA.77

Assay

≥98% (HPLC)

form

solid

optical activity

[α]23/D +11.0°, c = 1.08 in ethanol(lit.)

storage condition

protect from light

color

white

solubility

H2O: 10 mg/mL

SMILES string

Br.CCN1CCC[C@H]1CNC(=O)c2c(O)c(Cl)cc(Cl)c2O

InChI

1S/C14H18Cl2N2O3.BrH/c1-2-18-5-3-4-8(18)7-17-14(21)11-12(19)9(15)6-10(16)13(11)20;/h6,8,19-20H,2-5,7H2,1H3,(H,17,21);1H/t8-;/m0./s1

InChI key

RIWAHQQBHAKCTN-QRPNPIFTSA-N

Application

Precursor to radiolabeled S-(+)-raclopride.

Caution

Light sensitive

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

D204-VAR:
D204-1MG:
D204-5MG:
D204-BULK:


Certificates of Analysis (COA)

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M J Adam et al.
International journal of radiation applications and instrumentation. Part A, Applied radiation and isotopes, 40(1), 91-92 (1989-01-01)
This paper describes the separation of lipophilic amine radiopharmaceuticals on normal phase silica using a reversed phase type eluant. This class of compound usually gives very poor peak symmetry on reversed phase columns. However, excellent separation of a number of
V W Pike et al.
International journal of radiation applications and instrumentation. Part A, Applied radiation and isotopes, 41(5), 483-492 (1990-01-01)
Practical methods are described for the quality assurance of three labelled agents (L-6-[18F]fluoro-DOPA, S-[N-methyl-11C]nomifensine and [O-methyl-11C]raclopride) now produced regularly for PET studies of the dopaminergic system in man. These include indirect methods for the initial determination of label position (e.g.

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