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Merck
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02712

SAFC

Cystamine dihydrochloride

Fabrication pharma

Synonyme(s) :

2,2′-Diaminodiethyl disulfide dihydrochloride, 2,2′-Dithiobis(ethylamine) dihydrochloride, Decarboxycystine dihydrochloride

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About This Item

Formule linéaire :
NH2CH2CH2SSCH2CH2NH2 · 2HCl
Numéro CAS:
56-17-7
Poids moléculaire :
225.20
Numéro Beilstein :
3616850
Numéro CE :
200-260-7
Numéro MDL:
MFCD00012905
Code UNSPSC :
12352100
Nomenclature NACRES :
NA.21

Source biologique

synthetic

Niveau de qualité

500

Pureté

≥98.0% (TLC)

Concentration

≥98 % (w/w) (T)

Impuretés

≤100 mg/kg 2,6-Di-tert-butyl-4-methylphenol (BHT) (HPLC)
≤100 ppm 1,2-dimethoxyethan
≤5000 ppm tert-butyl methyl ether
≤5000 ppm ethanol

Pf

215-225 °C (dec.)
217-220 °C (dec.) (lit.)

Solubilité

H2O: 1.0 g/10 mL, clear to almost clear, colorless to almost colorless (<5.5 NTU)

Adéquation

corresponds for H-NMR

Chaîne SMILES 

Cl[H].Cl[H].NCCSSCCN

InChI

1S/C4H12N2S2.2ClH/c5-1-3-7-8-4-2-6;;/h1-6H2;2*1H

Clé InChI

YUFRRMZSSPQMOS-UHFFFAOYSA-N

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Pictogrammes

Exclamation mark
GHS07

Mention d'avertissement

Warning

Mentions de danger

H302

Classification des risques

Acute Tox. 4 Oral

Code de la classe de stockage

11 - Combustible Solids

Classe de danger pour l'eau (WGK)

WGK 3

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable

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Certificats d'analyse (COA)

Lot/Batch Number
BCCB2795
BCCB2794
BCBZ6822
BCBZ5212
BCBZ4055

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Consulter la Bibliothèque de documents

Yasue Ishii-Osai et al.
Journal of dermatological science, 67(1), 51-60 (2012-05-25)
N-propionyl-4-S-cysteaminylphenol (NPr-4-S-CAP) is selectively incorporated into melanoma cells and degrades them. However, it remains unclear whether NPr-4-S-CAP can induce cell death associated with the induction of host immune responses and tumor suppression in vivo. To examine the molecular mechanism of
Shosuke Ito et al.
Biochemical pharmacology, 84(5), 646-653 (2012-06-26)
Metastatic melanoma is resistant to conventional therapies. N-propionyl-4-S-cysteaminylphenol (NPrCAP), an N-protected sulfur-amine analog of tyrosine, is a good substrate for tyrosinase and is selectively incorporated into melanoma cells, causing cytotoxicity in vitro and in vivo. We have recently shown that
Thorsten Overath et al.
Molecular & cellular proteomics : MCP, 11(8), 467-477 (2012-05-05)
The post-translational modification of proteins with O-GlcNAc is involved in various cellular processes including signal transduction, transcription, translation, and nuclear transport. This transient protein modification enables cells or tissues to adapt to nutrient conditions or stress. O-Glycosylation of the 26
Zhongshan Liu et al.
Journal of chromatography. A, 1342, 70-77 (2014-04-15)
A polyhedral oligomeric silsesquioxane (POSS) hybrid monolith was simply prepared by using octaglycidyldimethylsilyl POSS (POSS-epoxy) and cystamine dihydrochloride as monomers via ring-opening polymerization. The effects of composition of prepolymerization solution and polycondensation temperature on the morphology and permeability of monolithic
Liang Gao et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 18(11), 3185-3192 (2012-02-22)
Autofluorescent microcapsules were assembled by covalent cross-linking of polysaccharide alginate dialdehyde (ADA) derivative and cystamine dihydrochloride (CM) through a layer-by-layer (LBL) technique. The formulated Schiff base and disulfide bonds render capsules with pH- and redox-responsive properties for pinpointed intracellular delivery
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