추천 제품
분석
98%
형태
solid
mp
>300 °C (lit.)
solubility
chloroform: soluble 10 mg/mL
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
유사한 제품을 찾으십니까? 방문 제품 비교 안내
일반 설명
Hexabromobenzene is used as fire retardant in plastics, paper and electric manufactured goods. It undergoes protodebromination when treated with sodium methoxide in methanol and ethyl methyl ketone to give a mixture of tetrabromobenzenes.
애플리케이션
The porphyrinogenic potential of hexabromobenzene (HBB) with hexachlorobenzene was studied in the liver of primiparous rats.
신호어
Warning
유해 및 위험 성명서
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
표적 기관
Respiratory system
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point (°F)
Not applicable
Flash Point (°C)
Not applicable
시험 성적서(COA)
제품의 로트/배치 번호를 입력하여 시험 성적서(COA)을 검색하십시오. 로트 및 배치 번호는 제품 라벨에 있는 ‘로트’ 또는 ‘배치’라는 용어 뒤에서 찾을 수 있습니다.
이미 열람한 고객
Uptake of chloro- and bromobiphenyls, hexachloro- and hexabromobenzene by fish.
Bulletin of environmental contamination and toxicology, 16(6), 665-673 (1976-12-01)
Polyhalogeno-aromatic compounds. Part VIII. Reactions of hexabromobenzene with nucleophiles.
J. Chem. Soc. Sect. C, 18, 2337-2341 (1969)
Comparison of the porphyrinogenic activity of hexabromobenzene and hexachlorobenzene in primiparous Wistar rats.
Bulletin of environmental contamination and toxicology, 21(3), 358-364 (1979-02-01)
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
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
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