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57857

Sigma-Aldrich

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
Beilstein:
4208524
EC Number:
265-905-7
MDL number:
MFCD00037273
UNSPSC Code:
12352103
PubChem Substance ID:
57651632
NACRES:
NA.25

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

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Application

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

Caution

May discolor to yellow on storage

Other Notes

Sales restrictions may apply

Pictograms

Exclamation mark
GHS07

Signal Word

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 Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

ISHL Indicated Name

Substances Subject to be Indicated Names

ISHL Notified Names

Substances Subject to be Notified Names

JAN Code

57857-50G-F:4548173995168
57857-10G-F:
57857-VAR-F:
57857-INTR-F:
57857-1KG-F:4548173995151
57857-BULK-F:

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’.

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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
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Experimental & molecular medicine, 43(10), 561-570 (2011-07-29)
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Journal of the science of food and agriculture, 91(13), 2437-2442 (2011-06-28)
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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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Journal of pharmaceutical and biomedical analysis, 123, 173-178 (2016-02-26)
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