T31003
Thiolactic acid
95%
Synonym(s):
2-Mercaptopropionic acid
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About This Item
Linear Formula:
CH3CH(SH)COOH
CAS Number:
Molecular Weight:
106.14
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
201-206-5
Beilstein/REAXYS Number:
506218
MDL number:
Assay:
95%
InChI key
PMNLUUOXGOOLSP-UHFFFAOYSA-N
InChI
1S/C3H6O2S/c1-2(6)3(4)5/h2,6H,1H3,(H,4,5)
SMILES string
CC(S)C(O)=O
assay
95%
refractive index
n20/D 1.481 (lit.)
bp
102 °C/16 mmHg (lit.), 203-208 °C (lit.)
mp
10-14 °C (lit.)
density
1.196 g/mL at 25 °C (lit.)
Quality Level
Application
Thiolactic acid (TLA) can be used as a building block in the synthesis of:
It can also be used as a bidental chelating agent for the surface modification of titanium dioxide (TiO2) nanoparticles for the removal of cadmium from waste water.
- Thiolactomycin via oxathiolanone intermediate.
- 4-Thiazolidinones by reacting various Schiff bases with thioglycolic acid.
- 1,4-Naphthoquinone derivatives containing sulfur atom for antibacterial and antiviral activity studies.
It can also be used as a bidental chelating agent for the surface modification of titanium dioxide (TiO2) nanoparticles for the removal of cadmium from waste water.
signalword
Danger
hcodes
Hazard Classifications
Skin Corr. 1B
Storage Class
6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials
wgk
WGK 1
flash_point_f
190.4 °F - closed cup
flash_point_c
88 °C - closed cup
ppe
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
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Synthesis and biological evaluation of novel 1, 4-naphthoquinone derivatives as antibacterial and antiviral agents
Tandon VK, et al.
Bioorganic & Medicinal Chemistry Letters, 15(14), 3463-3466 (2005)
Synthesis of novel heterocyclic 4-thiazolidinone derivatives and their antibacterial activity
Mistry KM and Desai KR
Journal of Chemistry, 1(4), 189-193 (2004)
Cadmium removal from water using thiolactic acid-modified titanium dioxide nanoparticles
Skubal LR, et al.
Journal of Photochemistry and Photobiology A: Chemistry, 148(1-3), 393-397 (2002)
A Flexible Route to (5 R)-Thiolactomycin, a Naturally Occurring Inhibitor of Fatty Acid Synthesis
McFadden JM, et al.
Organic Letters, 4(22), 3859-3862 (2002)
Yunbo Jiang et al.
Chemical communications (Cambridge, England), (44)(44), 6828-6830 (2009-11-04)
Addition of O(2)(g) at low-temperature to a mononuclear, nonheme iron(ii) complex comprising a tetraazamacrocyclic N(4) donor and an arylthiolate S donor leads to the generation of a deep red complex assigned as a low-spin Fe(III)?OOH complex, formed via metal- and
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