Skip to Content
Merck
All Photos(1)

Documents

63768

Sigma-Aldrich

3-Mercaptopropionic acid

≥99.0% (HPLC)

Synonym(s):

3-MPA, 3-Sulfanylpropanoic acid, beta-Mercaptopropionic acid

Sign Into View Organizational & Contract Pricing


About This Item

Linear Formula:
HSCH2CH2CO2H
CAS Number:
Molecular Weight:
106.14
Beilstein:
773807
EC Number:
MDL number:
UNSPSC Code:
12352103
PubChem Substance ID:
NACRES:
NA.26

vapor pressure

0.04 mmHg ( 20 °C)

Assay

≥99.0% (HPLC)

form

liquid

autoignition temp.

662 °F

refractive index

n20/D 1.492 (lit.)
n20/D 1.493

bp

110-111 °C/15 mmHg (lit.)

mp

15-18 °C (lit.)

density

1.218 g/mL at 25 °C (lit.)

absorption

cut-off at 270 nm

SMILES string

OC(=O)CCS

InChI

1S/C3H6O2S/c4-3(5)1-2-6/h6H,1-2H2,(H,4,5)

InChI key

DKIDEFUBRARXTE-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

Application

suitable for amino acid analysis by means of OPA

Other Notes

High-speed RP-HPLC/FC analysis of amino acids

Pictograms

Skull and crossbonesCorrosion

Signal Word

Danger

Hazard Statements

Hazard Classifications

Acute Tox. 3 Oral - Acute Tox. 4 Inhalation - Eye Dam. 1 - Met. Corr. 1 - Skin Corr. 1B

Storage Class Code

6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

WGK

WGK 1

Flash Point(F)

200.1 °F - closed cup

Flash Point(C)

93.4 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

T. Bartok et al.
Journal of Liquid Chromatography, 17, 4391-4391 (1994)
Brandon L Greene et al.
Journal of the American Chemical Society, 134(27), 11108-11111 (2012-06-22)
We report photocatalytic H(2) production by hydrogenase (H(2)ase)-quantum dot (QD) hybrid assemblies. Quenching of the CdTe exciton emission was observed, consistent with electron transfer from the quantum dot to H(2)ase. GC analysis showed light-driven H(2) production in the presence of
Qiang Wu et al.
International journal of nanomedicine, 7, 3433-3443 (2012-08-01)
Quantum dots (QDs) show promise as novel nanomaterials for sentinel lymph node (SLN) mapping through their use in noninvasive in vivo fluorescence imaging, and they have provided remarkable results. However, in vivo fluorescence imaging has limitations mainly reflected in the
Hui Zhang et al.
Chemical communications (Cambridge, England), 48(4), 567-569 (2012-01-19)
Water-soluble fluorescent copper, silver and gold nanoclusters with quantum yields of 2.2, 6.8 and 5.3%, respectively, are prepared by a robust photoreduction of their inorganic precursors in the presence of poly (methacrylic acid) functionalized with pentaerythritol tetrakis 3-mercaptopropionate.
Benoît M R Liénard et al.
Journal of medicinal chemistry, 51(3), 684-688 (2008-01-22)
The use of protein ESI mass spectrometry under non-denaturing conditions to analyze a dynamic combinatorial library of thiols/disulfides with the BcII metallo-beta-lactamase enabled the rapid identification of an inhibitor with a K(i) of < 1 microM. The study exemplifies the

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service