Cacodylate

HCID 167250

Basic information

CAS
15132-04-4
Standard SMILES
C[As](C)(=O)[O-]
InChIKey
OGGXGZAMXPVRFZ-UHFFFAOYSA-M
Molecular formula
C2H6AsO2-
Average molar mass
136.99 g/mol
Monoisotopic mass
136.95892451

Overview

Dimethylarsinate is the arsenic oxoanion that is the conjugate base of dimethylarsinic acid. It is functionally related to an arsinate. It is a conjugate base of a dimethylarsinic acid.

Names & identifiers

Preferred name
Cacodylate
IUPAC
dimethylarsinate
English name
Dimethylarsinate
Molecular formula
C2H6AsO2-
Molecular weight
136.98944

Names & synonyms

DimethylarsinateCacodylateCHEBI:16223RefChem:917815Cacodylate Ion15132-04-4Arsinic acid, dimethyl-, ion(1-)BollsDimethylarsonic Acidrad-e-cat 25Cacodylate ionsCacodylic acid, free acid
Show more names
KakodylatDMAVMe2AsO2(-)BDBM92451DTXSID60164758OGGXGZAMXPVRFZ-UHFFFAOYSA-M[As(CH3)2O2](-)Scotts Spot Grass and Weed Control

Database identifiers

CAS
15132-04-4
PubChem CID
167250
DTXSID
DTXSID60164758
ChEBI
CHEBI:16223
Nikkaji
J209.521A

Properties

Computed structural properties

Topological polar surface area
40.1 Ų
Hydrogen bond donors
0
Hydrogen bond acceptors
2
Rotatable bonds
0
Heavy atoms
5

Safety & regulation

Toxicology

Treatment · 1 item

Arsenic poisoning can be treated by chelation therapy, using chelating agents such as dimercaprol, EDTA or DMSA. Charcoal tablets may also be used for less severe cases. In addition, maintaining a diet high in sulfur helps eliminate arsenic from the body. (L20)

Health EffectsArsenic poisoning can lead to death from multi-system organ failure, probably from necrotic cell death, not apoptosis. Arsenic is also a known carcinogen, especially in skin, liver, bladder and lung cancers. (T1, L20)
Exposure RoutesOral (L2) ; inhalation (L2); dermal (L2)
Toxicity Summary · 1 item

Arsenic and its metabolites disrupt ATP production through different mechanisms. At the level of the citric acid cycle, arsenic inhibits the pyruvate dehydrogenase and uncouples the oxidative phosphorylation by competing with phosphate. This leads to inhibition of energy-linked reduction of NAD+, mitochondrial respiration, and ATP synthesis. Hydrogen peroxide production is increased, leading to oxidative stress due to the formation of reactive oxygen species. Arsenic's carginogenicity is influenced by the arsenical binding of tubulin, which results in aneuploidy, polyploidy and mitotic arrests. The binding of other arsenic protein targets may also cause altered DNA repair enzyme activity, altered DNA methylation patterns and cell proliferation. (T1, A17)

Signs and Symptoms · 1 item

Exposure to lower levels of arsenic can cause nausea and vomiting, decreased production of red and white blood cells, abnormal heart rhythm, damage to blood vessels, and a sensation of “pins and needles” in hands and feet. Breathing high levels of inorganic arsenic can provoque sore throat or irritated lungs. Arsenic also affects the brain, causing neurological disturbances such as headaches, confusion, and drowsiness. (A1)

Carcinogen Classification2B, possibly carcinogenic to humans. (L135)

Chemistry & industry

Pharmacology

Metabolism/MetabolitesArsenic and its metabolites are primarily excreted in the urine. (L2)
MeSH Pharmacological ClassificationPesticides used to destroy unwanted vegetation, especially various types of weeds, grasses (POACEAE), and woody plants. Some plants develop HERBICIDE RESISTANCE.

Uses & manufacturing

UsesDimethylarsinic acid is used as an herbicide and pesticide. (L180)

Suppliers1 total

杭州摩库生物医药科技有限公司+86-057181025280; +8617767106207 · [email protected]

Additional notes

DefinitionChEBI: Dimethylarsinate is the arsenic oxoanion that is the conjugate base of dimethylarsinic acid. It is functionally related to an arsinate. It is a conjugate base of a dimethylarsinic acid.

Related reactions

4 records

Compound notes

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