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408174

Sigma-Aldrich

S-Benzylcysteamine hydrochloride

99%

Synonym(s):

2-(Benzylthio)ethylamine hydrochloride

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About This Item

Linear Formula:
C6H5CH2SCH2CH2NH2·HCl
CAS Number:
22572-33-4
Molecular Weight:
203.73
MDL number:
MFCD00191774
UNSPSC Code:
12352100
PubChem Substance ID:
24865510
Pricing and availability is not currently available.

Assay

99%

form

solid

mp

126-127 °C (lit.)

functional group

amine
phenyl
thioether

SMILES string

Cl.NCCSCc1ccccc1

InChI

1S/C9H13NS.ClH/c10-6-7-11-8-9-4-2-1-3-5-9;/h1-5H,6-8,10H2;1H

InChI key

XZXIWQYIVDFDSP-UHFFFAOYSA-N

General description

S-Benzylcysteamine hydrochloride is sulphur containing organic building block. It is reported to afford S-benzylcysteamine on reaction with 0.1M methanolic NaOMe .[1]

Application

S-Benzylcysteamine hydrochloride may be employed as starting reagent in the synthesis of mercaptoacetyltriglycine (MAG3) derivatives.[2]

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H315,H319,H335

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

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

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Certificates of Analysis (COA)

Lot/Batch Number
21110TA
15323JF
09925HC
08408LS

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Synthesis and biological characteristics of the Technetium-99m triamide derivatives of mercaptoacetyltriglycine (MAG3).
Okarvi SM, et al.
Journal of Labelled Compounds & Radiopharmaceuticals, 46(1), 73-84 (2003)
Designer ligands. VIII. Thermal and microwave-assisted synthesis of silver (I)-selective ligands.
Daubinet A and Kaye PT.
Synthetic Communications, 32(20), 3207-3217 (2002)

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