18720
氢溴酸 溶液
purum p.a., ≥62% (T)
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关于此项目
经验公式（希尔记法）:
HBr
化学文摘社编号:
分子量:
80.91
PubChem Substance ID:
UNSPSC Code:
12352106
Beilstein/REAXYS Number:
3587158
MDL number:
SMILES string
Br
InChI
1S/BrH/h1H
InChI key
CPELXLSAUQHCOX-UHFFFAOYSA-N
grade
purum p.a.
assay
≥62% (T)
form
liquid
density
1.723 g/cm3
anion traces
sulfate, sulfite (as SO42-): ≤50 mg/kg
cation traces
Ca: ≤10 mg/kg, Cd: ≤5 mg/kg, Co: ≤5 mg/kg, Cr: ≤5 mg/kg, Cu: ≤5 mg/kg, Fe: ≤5 mg/kg, K: ≤50 mg/kg, Mg: ≤5 mg/kg, Mn: ≤5 mg/kg, Na: ≤50 mg/kg, Ni: ≤5 mg/kg, Pb: ≤5 mg/kg, Zn: ≤5 mg/kg
signalword
Danger
hcodes
Hazard Classifications
Eye Dam. 1 - Met. Corr. 1 - Skin Corr. 1B - STOT SE 3
target_organs
Respiratory system
存储类别
8B - Non-combustible corrosive hazardous materials
wgk
WGK 1
flash_point_f
Not applicable
flash_point_c
Not applicable
法规信息
新产品
此项目有
Study of chemical reaction mechanisms with molecular beams. The reaction of K with HBr.
Taylor EH and Datz S.
J. Chem. Phys. , 23(9), 1711-1718 (1955)
Improved infrared spectroscopic method for the analysis of degree of N-deacetylation of chitosan.
Sabnis S and Block LH.
Polym. Bull., 39(1), 67-71 (1997)
Małgorzata Olejniczak et al.
The Journal of chemical physics, 136(1), 014108-014108 (2012-01-14)
We report the implementation of nuclear magnetic resonance (NMR) shielding tensors within the four-component relativistic Kohn-Sham density functional theory including non-collinear spin magnetization and employing London atomic orbitals to ensure gauge origin independent results, together with a new and efficient
Po-Yu Tsai et al.
Physical chemistry chemical physics : PCCP, 13(4), 1419-1423 (2010-11-27)
The orientation dependence of Br-atom formation in the reaction of the oriented OH radical with the HBr molecule using the hexapole electrostatic field was studied. Experimental results for the orientation dependence in the reaction were analyzed using a Legendre polynomial
Saron Catak et al.
The Journal of organic chemistry, 75(13), 4530-4541 (2010-05-29)
Ring opening of 1-arylmethyl-2-(cyanomethyl)aziridines with HBr afforded 3-(arylmethyl)amino-4-bromobutyronitriles via regiospecific ring opening at the unsubstituted aziridine carbon. Previous experimental and theoretical reports show treatment of the same compounds with benzyl bromide to furnish 4-amino-3-bromobutanenitriles through ring opening at the substituted
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