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T30201

Sigma-Aldrich

3,3′-Thiodipropionic acid

97%

Synonym(s):

Bis(2-carboxyethyl) sulfide

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About This Item

Linear Formula:
S(CH2CH2COOH)2
CAS Number:
111-17-1
Molecular Weight:
178.21
Beilstein:
1210299
EC Number:
203-841-3
MDL number:
MFCD00002781
UNSPSC Code:
12352100
PubChem Substance ID:
24900099
NACRES:
NA.22

Quality Level

200

Assay

97%

mp

131-134 °C (lit.)

SMILES string

OC(=O)CCSCCC(O)=O

InChI

1S/C6H10O4S/c7-5(8)1-3-11-4-2-6(9)10/h1-4H2,(H,7,8)(H,9,10)

InChI key

ODJQKYXPKWQWNK-UHFFFAOYSA-N

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Application

3,3′-Thiodipropionic acid is an organic disulfide that can be used as a ligand for the synthesis of cadminum and zinc coordination polymers with luminescent properties.

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H319

Hazard Classifications

Eye Irrit. 2

Storage Class Code

11 - Combustible Solids

WGK

WGK 1

Flash Point(F)

262.4 °F - closed cup

Flash Point(C)

128 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Synthesis, Structure, and Luminescence Properties of Zinc (II) and Cadmium (II) Complexes containing the Flexible Ligand of 3, 3??Thiodipropionic Acid.
Yang P, et al.
Zeitschrift fur Anorganische und Allgemeine Chemie, 634(6?7), 1221-1224 (2008)
Hong-Seok Kim et al.
Foodborne pathogens and disease, 14(2), 84-88 (2017-01-05)
Culture-based detection of nontyphoidal Salmonella spp. in foods requires at least four working days; therefore, new detection methods that shorten the test time are needed. In this study, we developed a novel single-step Salmonella enrichment broth, SSE-1, and compared its
E Fehling et al.
Biotechnology and bioengineering, 99(5), 1074-1084 (2007-10-31)
Linear copolymeric polyesters (polyoxoesters) containing thioether functions [poly(3,3'-thiodipropionic acid-co-alpha,omega-alkanediols)] were formed in good yield by esterification of an equimolar mixture of 3,3'-thiodipropionic acid (4-thiaheptane-1,7-dioic acid) and 1,6-hexanediol (weight average molecular mass, M(W) >600 Da: approximately 81% after 6 h) or
Spontaneously organized molecular assemblies. 3. Preparation and properties of solution adsorbed monolayers of organic disulfides on gold surfaces.
Nuzzo R, et al.
Journal of the American Chemical Society, 109(8), 2358-2368 (1987)
Yasutaka Kamei et al.
Macromolecular bioscience, 7(3), 364-372 (2007-03-21)
To prepare sulfur-containing natural polymers effectively, several plant oils and 3,3'-thiodipropionic acid (TDP) have been used as carbon sources for the biosynthesis of copolymer poly[(3-hydroxybutyrate)-co-(3-mercaptopropionate)] [poly(3HB-co-3MP)] by a wild-type bacterium Cupriviadus necator H16. By using the plant oils, copolymer accumulation
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