C0125
二甲基胂酸
≥98%
别名:
二甲次胂酸, 二甲胂酸, 羟基二甲基氧化胂
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关于此项目
线性分子式:
(CH3)2As(O)OH
化学文摘社编号:
分子量:
138.00
UNSPSC Code:
12161700
NACRES:
NA.25
PubChem Substance ID:
EC Number:
200-883-4
Beilstein/REAXYS Number:
1736965
MDL number:
InChI
1S/C2H7AsO2/c1-3(2,4)5/h1-2H3,(H,4,5)
SMILES string
C[As](C)(O)=O
InChI key
OGGXGZAMXPVRFZ-UHFFFAOYSA-N
assay
≥98%
form
powder
solubility
water: 50 mg/mL, clear, colorless
Quality Level
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signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Carc. 1B
存储类别
6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
法规信息
危险化学品
此项目有
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Fang-Chih Chang et al.
Talanta, 198, 137-145 (2019-03-17)
An analytical method for the biomonitoring of arsenic, benzene and polycyclic aromatic hydrocarbons (PAHs) in human urine was developed using liquid chromatography tandem mass spectrometry (LC-MS/MS). The urinary metabolites of monomethylarsonic acid (MMAA), dimethylarsonic acid (DMAA), s-phenylmercapturic acid (S-PMA), and
E M Kenyon et al.
Toxicology, 160(1-3), 227-236 (2001-03-14)
Dimethylarsinic acid (DMA) has been used as a herbicide (cacodylic acid) and is the major metabolite formed after exposure to tri- (arsenite) or pentavalent (arsenate) inorganic arsenic (iAs) via ingestion or inhalation in both humans and rodents. Once viewed simply
Larissa Leffers et al.
Toxicology, 305, 109-119 (2013-01-29)
Inorganic arsenic is a well-documented, exposure relevant human carcinogen. A promising starting point to further understand the mechanisms behind inorganic arsenic carcinogenicity might be a formation of reactive, highly toxic metabolites during human arsenic metabolism. This study characterises the toxicity
Erik J Tokar et al.
Toxicology letters, 209(2), 179-185 (2012-01-11)
Inorganic arsenic, an early life carcinogen in humans and mice, can initiate lesions promotable by other agents in later life. The biomethylation product of arsenic, dimethylarsinic acid (DMA), is a multi-site tumor promoter. Thus, pregnant CD1 mice were given drinking
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