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C121509

Sigma-Aldrich

Cystamine dihydrochloride

96%

Sinonimo/i:

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

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About This Item

Formula condensata:
NH2CH2CH2SSCH2CH2NH2 · 2HCl
Numero CAS:
56-17-7
Peso molecolare:
225.20
Beilstein:
3616850
Numero CE:
200-260-7
Numero MDL:
MFCD00012905
Codice UNSPSC:
12352100
ID PubChem:
24892384
NACRES:
NA.22

Saggio

96%

Forma fisica

powder

Punto di fusione

217-220 °C (dec.) (lit.)

Stringa SMILE

Cl[H].Cl[H].NCCSSCCN

InChI

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

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Categorie correlate

Applicazioni

Cystamine dihydrochloride can be utilized as a building block in the synthesis of disulfide cross-linked oligodeoxyribonucleotides and psammaplin A . It can be also used to functionalize PGMA (poly(glycidyl methacrylate) microsphere) by introducing sulfhydryl groups for the further fabrication of silver nanoparticles (AgNPs).
Heparin antagonist and sulfhydryl modifying reagent

Prodotti correlati

N° Catalogo
Descrizione
Determinazione del prezzo

914592

Fmoc-Cystamine HCl, ≥95%

Pittogrammi

Exclamation mark
GHS07

Avvertenze

Warning

Indicazioni di pericolo

H302

Classi di pericolo

Acute Tox. 4 Oral

Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable

Dispositivi di protezione individuale

dust mask type N95 (US), Eyeshields, Gloves

Certificati d'analisi (COA)

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Cysteamine hydrochloride ≥97.0% (RT)

Sigma-Aldrich

30080

Cysteamine hydrochloride

2-Hydroxyethyl disulfide technical grade

Sigma-Aldrich

380474

2-Hydroxyethyl disulfide

Cysteamine hydrochloride analytical standard

Supelco

49705

Cysteamine hydrochloride

3,3′-Dithiodipropionic acid 99%

Sigma-Aldrich

109010

3,3′-Dithiodipropionic acid

Cysteamine hydrochloride BioXtra

Sigma-Aldrich

30078

Cysteamine hydrochloride

Bis(11-azidoundecyl) disulfide 99% (HPLC)

Sigma-Aldrich

701300

Bis(11-azidoundecyl) disulfide

Synthesis and characterization of disulfide cross-linked oligonucleotides
Ferentz A E, et al.
Journal of the American Chemical Society, 115(20), 9006-9014 (1993)
In situ synthesis of monodisperse silver nanoparticles on sulfhydryl-functionalized poly (glycidyl methacrylate) microspheres for catalytic reduction of 4-nitrophenol
Zhang W, et al.
Industrial & Engineering Chemistry Research, 54(25), 6480-6488 (2015)
Qianjiao Yang et al.
Molecules (Basel, Switzerland), 15(12), 8784-8795 (2010-12-04)
Psammaplin F, an unsymmetrical disulfide bromotyrosine, was isolated from the sponge Pseudoceratina purpurea in 2003. We reported here the first total synthesis of psammaplin F in 12% overall yield by employing Cleland's reagent reduction as key step. The longest linear
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
Jie Gao et al.
Langmuir : the ACS journal of surfaces and colloids, 28(9), 4464-4471 (2012-01-27)
Gold nanoparticles (GNPs) are attractive alternative optical probes and good biocompatible materials due to their special physical and chemical properties. However, GNPs have a tendency to aggregate particularly in the presence of high salts and certain biological molecules such as
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