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57857

Lithium iodoacetate

≥97.0% (NT)

Synonym(s):

Iodoacetic acid lithium salt

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About This Item

Linear Formula:
ICH2COOLi
CAS Number:
65749-30-6
Molecular Weight:
191.88
UNSPSC Code:
12352103
NACRES:
NA.25
PubChem Substance ID:
57651632
EC Number:
265-905-7
Beilstein/REAXYS Number:
4208524
MDL number:
MFCD00037273
Assay:
≥97.0% (NT)

Quality Level

200

assay

≥97.0% (NT)

impurities

≤3% water

mp

239 °C (dec.) (lit.), ~245 °C (dec.)

SMILES string

[Li+].[O-]C(=O)CI

InChI

1S/C2H3IO2.Li/c3-1-2(4)5;/h1H2,(H,4,5);/q;+1/p-1

InChI key

RZCFQIDTJPHHFJ-UHFFFAOYSA-M

Application

Lithium iodoacetate, a halogenacetate, is a lithium salt of iodoacetate that may be used in the study of cysteine peptidases.

Other Notes

Sales restrictions may apply

Disclaimer

May discolor to yellow on storage

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Lithium iodoacetate ≥97.0% (NT)

Sigma-Aldrich

57857

Lithium iodoacetate

Lithium palmitate ≥97.0% (NT)

Sigma-Aldrich

76128

Lithium palmitate

Lithium β-hydroxypyruvate hydrate ≥97.0% (calc. based on dry substance, NT)

Sigma-Aldrich

54913

Lithium β-hydroxypyruvate hydrate

Lithium carbonate ACS reagent, ≥99.0%

Sigma-Aldrich

255823

Lithium carbonate

assay

≥97.0% (NT)

assay

≥97.0% (NT)

assay

≥97.0% (calc. based on dry substance, NT)

assay

≥99.0%

Quality Level

200

Quality Level

100

Quality Level

100

Quality Level

200

mp

239 °C (dec.) (lit.), ~245 °C (dec.)

mp

226-229 °C

mp

-

mp

618 °C (lit.)

impurities

≤3% water

impurities

-

impurities

~1 mol water

impurities

≤0.01% insol. dil. HCl, ≤0.2% S compounds

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - 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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Certificates of Analysis (COA)

Lot/Batch Number
BCBV9871
BCBK8828V
BCBF2657V
BCBF0346V
BCBC4151V

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Ehrenberg et al.
Acta crystallographica. Section B, Structural science, 55(Pt 4), 517-524 (2000-08-06)
Most halogenoacetates of alkali salts readily undergo a thermally induced polymerization reaction to poly-(hydroxyacetic acid) in the solid state. The lithium salts represent a remarkable exception. The crystal structures of lithium chloroacetate, lithium bromoacetate and lithium iodoacetate were determined ab
Yun Ju Woo et al.
Experimental & molecular medicine, 43(10), 561-570 (2011-07-29)
Osteoarthritis (OA) is an age-related joint disease that is characterized by degeneration of articular cartilage and chronic pain. Oxidative stress is considered one of the pathophysiological factors in the progression of OA. We investigated the effects of grape seed proanthocyanidin
Sébastien Goutal et al.
Drug delivery and translational research, 8(3), 536-542 (2018-01-03)
Elacridar (GF120918) is a highly potent inhibitor of both P-glycoprotein (ABCB1) and breast cancer resistance protein (ABCG2), the main efflux transporters expressed at the blood-brain barrier (BBB). Elacridar shows very low aqueous solubility, which complicates its formulation for i.v. administration.
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Global Trade Item Number

SKUGTIN
57857-50G-F04061832860398
57857-1KG-F04061832629223

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