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I10457

3-Iodopropionic acid

Name: 3-Iodopropionic acid
Brand: ALDRICH

95%

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About This Item

Fórmula lineal:

ICH₂CH₂CO₂H

Número de CAS:

141-76-4

Peso molecular:

199.98

EC Number:

205-499-0

MDL number:

MFCD00002765

UNSPSC Code:

12352100

PubChem Substance ID:

24895919

NACRES:

NA.22

assay

95%

mp

80-83 °C (lit.)

SMILES string

OC(=O)CCI

InChI

1S/C3H5IO2/c4-2-1-3(5)6/h1-2H2,(H,5,6)

InChI key

KMRNTNDWADEIIX-UHFFFAOYSA-N

Categorías relacionadas

Unidades estructurales orgánicas

Other Notes

Remainder 3-chloropropionic acid

pictograms

GHS05

signalword

Danger

hcodes

H314

pcodes

P260 - P280 - P303 + P361 + P353 - P304 + P340 + P310 - P305 + P351 + P338 - P363

Hazard Classifications

Eye Dam. 1 - Skin Corr. 1B

Storage Class

8A - Combustible corrosive hazardous materials

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges

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Nanostructured and Photochromic Material for Environmental Detection of Metal Ions.

Raphael C L Machado et al.

Molecules (Basel, Switzerland), 24(23) (2019-11-27)

Compared to conventional spectroscopy or chromatography analysis, chemical sensing based on colorimetric changes offers an alternative to monitor potential metal hazards in aqueous environment through rapid and low-cost colorimetric changes which can be easily interpreted. In this work poly(ethylene glycol)

Functional Characterization of a L-2-Haloacid Dehalogenase From Zobellia galactanivorans DsijT Suggests a Role in Haloacetic Acid Catabolism and a Wide Distribution in Marine Environments.

Eugénie Grigorian et al.

Frontiers in microbiology, 12, 725997-725997 (2021-10-09)

L-2-halocid dehalogenases (L-2-HADs) have been mainly characterized from terrestrial polluted environments. By contrast, knowledge is still scarce about their role in detoxification of predominant halocarbons in marine environments. Here, phylogenetic analyses showed a wide diversity of homologous L-2-HADs, especially among

Hemicyanine dyes derived from 2,3,3-trimethyl-3H-indolium as candidates for non-covalent protein probes.

Janina Kabatc et al.

Journal of pharmaceutical and biomedical analysis, 114, 433-440 (2015-06-30)

Non-covalent interaction of hemicyanine dyes, derivatives of 2,3,3-trimethyl-3H-indolium with bovine serum albumin has been studied by spectral method. For this purpose, three hemicyanine dyes containing N-(2-carboxyethyl)-2,3,3-trimethyl-3H-indolium moiety were synthesized and their UV/Vis and fluorescence spectra, aggregation, photostability and association with

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