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Merck
CN

45524

六溴苯

PESTANAL®, analytical standard

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关于此项目

经验公式(希尔记法):
C6Br6
化学文摘社编号:
分子量:
551.49
EC Number:
201-773-9
UNSPSC Code:
41116107
PubChem Substance ID:
Beilstein/REAXYS Number:
1912586
MDL number:
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grade

analytical standard

product line

PESTANAL®

shelf life

limited shelf life, expiry date on the label

technique(s)

HPLC: suitable, gas chromatography (GC): suitable

mp

>300 °C (lit.)

application(s)

agriculture
environmental

format

neat

SMILES string

Brc1c(Br)c(Br)c(Br)c(Br)c1Br

InChI

1S/C6Br6/c7-1-2(8)4(10)6(12)5(11)3(1)9

InChI key

CAYGQBVSOZLICD-UHFFFAOYSA-N

Application

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

Legal Information

PESTANAL is a registered trademark of Merck KGaA, Darmstadt, Germany


pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Aquatic Chronic 4 - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

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



历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Hans Peter H Arp et al.
Journal of environmental monitoring : JEM, 13(3), 505-513 (2010-12-09)
The brominated flame retardants (BFRs), pentabromotoluene (PBT), pentabromoethylbenzene (PBEB) and hexabromobenzene (HBB), exhibit physical-chemical properties similar to other persistent organic pollutants, and have been in use as flame retardants for several decades. Data on these BFRs in diverse environmental samples
Joanna Wencel-Delord et al.
Angewandte Chemie (International ed. in English), 51(52), 13001-13005 (2012-10-23)
C(6)Br(six) & drugs! C(6)Br(6) can be used as the cooxidant/catalyst modifier for the [Rh(III)Cp*]-catalyzed (Cp*=C(5)Me(5)) dehydrogenative cross-coupling of benzamides with simple benzene derivatives (see scheme, DG=directing group). Similarly, heterocycles can be coupled and druglike structures formed. Mechanistic studies suggest a
Alterations of uroporphyrinogen decarboxylase by chlorinated organics.
G H Elder et al.
Annals of the New York Academy of Sciences, 514, 141-147 (1987-01-01)