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线性分子式:
C2H5CH(Br)CO2H
化学文摘社编号:
分子量:
167.00
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
201-294-5
Beilstein/REAXYS Number:
1720950
MDL number:
Assay:
97%
Form:
liquid
产品名称
2-溴丁酸, 97%
InChI key
YAQLSKVCTLCIIE-UHFFFAOYSA-N
InChI
1S/C4H7BrO2/c1-2-3(5)4(6)7/h3H,2H2,1H3,(H,6,7)
SMILES string
CCC(Br)C(O)=O
assay
97%
form
liquid
refractive index
n20/D 1.474 (lit.)
bp
99-103 °C/10 mmHg (lit.)
mp
−4 °C (lit.)
solubility
water: soluble 15 part
alcohol: soluble
diethyl ether: soluble
density
1.567 g/mL at 25 °C (lit.)
Quality Level
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Application
2-Bromobutyric acid was used in the synthesis of S-(1-carboxypropyl)-L-cysteine.
signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Eye Dam. 1 - Skin Corr. 1B
存储类别
8A - Combustible corrosive hazardous materials
wgk
WGK 3
flash_point_f
No data available
flash_point_c
No data available
ppe
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
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The formation of toxic disinfection by-products (DBPs) is among the main concerns in the use of chlorine sanitizers for washing fresh and fresh-cut produce to minimize microbial cross-contamination. Even so, robust analytical methods for measuring various DBPs in produce have
W E Roediger et al.
Lipids, 25(10), 646-652 (1990-10-01)
Attempts were made to define which fatty acid (2:0 to 18:1) was optimally oxidized by isolated colonocytes (colonic epithelial cells) and to select inhibitors of fatty acid oxidation which would be analogous in their action to the inhibition of fatty
C Blarzino et al.
The Italian journal of biochemistry, 36(1), 1-7 (1987-01-01)
Details are reported for the synthesis of S-(1-carboxyethyl)-L-cysteine (1-CEC) and S-(1-carboxypropyl)-L-cysteine (1-CPC) from cysteine and 2-bromopropionic acid or 2-bromobutyric acid, respectively. Some analytical data and the behaviour of these two compounds on paper and ion-exchange chromatography are also reported, which
Yu-Syuan Luo et al.
Toxicology, 409, 33-43 (2018-07-28)
Trichloroethylene (TCE) and tetrachloroethylene (PCE) are structurally similar chemicals that are metabolized through oxidation and glutathione conjugation pathways. Both chemicals have been shown to elicit liver and kidney toxicity in rodents and humans; however, TCE has been studied much more
Milena E Miska et al.
Rapid communications in mass spectrometry : RCM, 29(24), 2341-2348 (2015-11-14)
The environmental occurrence of chlorinated acetic acids (CAAs) has been extensively studied, but the sources and transport are still not yet fully understood. A promising approach for source apportionment and process studies is the isotopic characterization of target compounds. We
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