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35597

Supelco

PCB No 15

analytical standard

Sinonimo/i:

4,4′-Dichlorobiphenyl, 4,4′-PCB

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100 MG
CHF 163.00

CHF 163.00

Spedizione prevista il26 maggio 2025

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100 MG
CHF 163.00

About This Item

Formula empirica (notazione di Hill):
C12H8Cl2
Numero CAS:
2050-68-2
Peso molecolare:
223.10
Beilstein:
2044700
Numero di Ballschmiter:
15
Numero CE:
218-095-4
Numero MDL:
MFCD00013641
Codice UNSPSC:
41116107
ID PubChem:
329755193
NACRES:
NA.24

CHF 163.00

Spedizione prevista il26 maggio 2025

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Grado

analytical standard

Livello qualitativo

100

Durata

limited shelf life, expiry date on the label

tecniche

HPLC: suitable
gas chromatography (GC): suitable

applicazioni

environmental

Formato

neat

Stringa SMILE

Clc1ccc(cc1)-c2ccc(Cl)cc2

InChI

1S/C12H8Cl2/c13-11-5-1-9(2-6-11)10-3-7-12(14)8-4-10/h1-8H
YTBRNEUEFCNVHC-UHFFFAOYSA-N

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Applicazioni

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Prodotti consigliati

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.

Pittogrammi

Health hazardEnvironment
GHS08,GHS09

Avvertenze

Warning

Indicazioni di pericolo

H373,H410

Classi di pericolo

Aquatic Acute 1 - Aquatic Chronic 1 - STOT RE 2

Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable

Dispositivi di protezione individuale

dust mask type N95 (US), Eyeshields, Gloves

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Certificati d'analisi (COA)

Lot/Batch Number
BCCM6188
BCCD6884
BCCD4578
BCBV0152

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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
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)
T A Marks et al.
Fundamental and applied toxicology : official journal of the Society of Toxicology, 13(4), 681-693 (1989-11-01)
Outbred albino (CD-1) mice were given the following biphenyl isomers by gavage in cottonseed oil on Days 6-15 of gestation: 4,4'-dichlorobiphenyl (DCB) at 16, 32, and 64 mg/kg/day; 3,3',4,4'-tetrachlorobiphenyl (3,4-TCB) at 1,2,4,8,16,32, and 64 mg/kg/day; 3,3',5,5'-tetrachlorobiphenyl (3,5-TCB) at 64 mg/kg/day;
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
R G Schnellmann et al.
Biochemical pharmacology, 33(21), 3503-3509 (1984-11-01)
Since chlorine placement and the degree of chlorination of the biphenyl nucleus play an important role in the metabolism and ultimate elimination of polychlorinated biphenyls (PCBs), we have studied the metabolism of 4,4'-dichlorobiphenyl (4-DCB) by human hepatic microsomes. This low
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