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About This Item
Linear Formula:
NH2CH2CH2SH
CAS Number:
Molecular Weight:
77.15
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
200-463-0
Beilstein/REAXYS Number:
635649
MDL number:
Product Name
Cysteamine, ~95%
InChI key
UFULAYFCSOUIOV-UHFFFAOYSA-N
InChI
1S/C2H7NS/c3-1-2-4/h4H,1-3H2
SMILES string
NCCS
assay
~95%
form
solid
storage temp.
2-8°C
Quality Level
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Application
Cysteamine is an amino thiol drug mainly used in the treatment of cystinosis. It is an antioxidant with chemo-sensitizing and radioprotective properties.
signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
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Ravendra Naidoo et al.
Bacteriophage, 2(1), 15-24 (2012-06-06)
Bacteriophages offer interesting alternatives to antibodies for the specific capture and detection of pathogenic bacteria onto biosensing surfaces. Procedures for the optimal chemical immobilization of lytic bacteriophages onto surfaces are presented. More specifically, the removal of lysate contaminants from bacteriophage
Cysteamine suppresses invasion, metastasis and prolongs survival by inhibiting matrix metalloproteinases in a mouse model of human pancreatic cancer.
Fujisawa T, et al.
PLoS ONE, 7(4), e34437-e34437 (2012)
Dandan Fang et al.
Mikrochimica acta, 186(9), 608-608 (2019-08-09)
An ultrasensitive competitive-type electrochemiluminescence immunoassay for the mycotoxin zearalenone is described. The method is based on the use of (a) a mimotope peptide that was selected from a phage displayed peptide library and used to substitute ZEN for designing the
Francesca Malvano et al.
Sensors (Basel, Switzerland), 18(7) (2018-07-07)
In this work, the development of an impedimetric label-free immunosensor for the detection of Escherichia coli O157:H7 is reported. Different immobilization techniques of monoclonal anti-E. coli were tested, in order to reach the very low limit of detections. The comparison
A de Graaf-Hess et al.
Clinical chemistry, 45(12), 2224-2228 (1999-12-10)
Cystinosis is a rare inborn error of cystine transport, leading to accumulation of cystine in the lysosomes. To diagnose cystinosis and monitor treatment with cysteamine, adequate measurements of cystine concentrations in leukocytes and cultured fibroblasts are required. Cells were sonicated
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