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经验公式(希尔记法):
C12H8Cl2
化学文摘社编号:
分子量:
223.10
EC Number:
218-095-4
UNSPSC Code:
41116107
NACRES:
NA.24
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
2044700
Ballschmiter Number:
15
InChI key
YTBRNEUEFCNVHC-UHFFFAOYSA-N
InChI
1S/C12H8Cl2/c13-11-5-1-9(2-6-11)10-3-7-12(14)8-4-10/h1-8H
SMILES string
Clc1ccc(cc1)-c2ccc(Cl)cc2
grade
analytical standard
shelf life
limited shelf life, expiry date on the label
technique(s)
HPLC: suitable, gas chromatography (GC): suitable
application(s)
environmental
format
neat
Quality Level
Application
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.
Other Notes
Find a digital Reference Material for this product available on our online platform ChemisTwin® for NMR. You can use this digital equivalent on ChemisTwin® for your sample identity confirmation and compound quantification (with digital external standard). An NMR spectrum of this substance can be viewed and an online comparison against your sample can be performed with a few mouseclicks. Learn more here and start your free trial.
signalword
Warning
hcodes
Hazard Classifications
Aquatic Acute 1 - Aquatic Chronic 1 - STOT RE 2
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
法规信息
监管及禁止进口产品
此项目有
Accumulation and excretion of isopropylchlorobiphenyls in mouse and fish.
K Sugiura et al.
Bulletin of environmental contamination and toxicology, 26(1), 46-53 (1981-01-01)
W Chu et al.
Water research, 37(10), 2442-2448 (2003-05-03)
The system design based on the photodegradation kinetics of 4,4'-dichlorobiphenyl (4,4'-DCB) in surfactant solution with the aid of solvents (acetone and/or squalane) has been studied. Organic solvents acetone and squalane were added as a photosensitizer and a hydrogen source, respectively
Ichiro Kamei et al.
Applied microbiology and biotechnology, 72(3), 566-575 (2006-03-11)
Degradation experiment of model polychlorinated biphenyl (PCB) compound 4,4'-dichlorobiphenyl (4,4'-DCB) and its metabolites by the white-rot fungus Phanerochaete chrysosporium and newly isolated 4,4'-DCB-degrading white-rot fungus strain MZ142 was carried out. Although P. chrysosporium showed higher degradation of 4,4'-DCB in low-nitrogen
B J Scholte et al.
European journal of biochemistry, 151(1), 67-73 (1985-08-15)
We have studied the induction of cytochrome P-450b,e-type antigen and mRNA by phenobarbital, 4,4'-dichlorobiphenyl and 2,4,5,2',4',5'-hexachlorobiphenyl in male Wistar rat liver. Chronic treatment of rats with 4,4'-dichlorobiphenyl leads to a relatively slow, 20-fold increase in the cytochrome P-450b,e-type antigen level
M T Scott et al.
Journal of pharmaceutical sciences, 73(8), 1171-1172 (1984-08-01)
A reverse-phase HPLC system was used for the determination of inorganic chloride liberated in vivo from two biphenyl compounds in the rat. Oral administration of [4-36Cl]chlorobiphenyl resulted in a total yield of 27.6% of the original dose excreted over 10
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