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About This Item
Linear Formula:
HOCOCH2CH2SSCH2CH2COOH
CAS Number:
Molecular Weight:
210.27
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
214-284-0
Beilstein/REAXYS Number:
1778543
MDL number:
Assay:
95%
InChI key
YCLSOMLVSHPPFV-UHFFFAOYSA-N
InChI
1S/C6H10O4S2/c7-5(8)1-3-11-12-4-2-6(9)10/h1-4H2,(H,7,8)(H,9,10)
SMILES string
OC(=O)CCSSCCC(O)=O
assay
95%
Quality Level
functional group
carboxylic acid, disulfide
Related Categories
General description
3,3′-Dithiodipropionic acid forms monolayers on a polycrystalline gold electrode through a self-assembly procedure to form gold 3,3′-dithiodipropionic acid self-assembled monolayer modified electrode. It is the precursor substrate in the synthesis of 3-mercaptopropionic acid-containing polythioesters. It is added as primary carbon supplement in the culture medium of novel betaproteobacterium, strain DPN7.
Application
3,3′-Dithiodipropionic acid was used as capping agent for introducing charge on gold nanoparticles surfaces.
signalword
Warning
hcodes
Hazard Classifications
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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Xiaoyou Xu et al.
Journal of chromatography. A, 1167(1), 35-41 (2007-09-07)
We employed agarose gel preparative electrophoresis to separate gold nanoparticles based on size, shape, and charge. The separating technique was first demonstrated by size separation of 5 nm, 15 nm, and 20 nm spherical gold nanoclusters; and further evidenced through
Lucia Codognoto et al.
Talanta, 72(2), 427-433 (2007-04-30)
Monolayers of 3,3'-dithiodipropionic acid (DTDPA) were prepared on a polycrystalline gold electrode through a self-assembly procedure to produce a gold 3,3'-dithiodipropionic acid self-assembled monolayer (AuDTDPA) modified electrode. The characterization of the AuDTDPA electrode was investigated by cyclic voltammetry and ac
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Stimuli-responsive nanocarriers for anticancer drug and gene co-delivery are promising strategy in cancer therapy. The ultimate goal is to deliver high local concentration of therapeutic agents with no premature release and result in synergistic effects for combination therapies. In this
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