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About This Item
Linear Formula:
(CH3)2CHC6Br2(CH3)(=O)2
CAS Number:
Molecular Weight:
321.99
NACRES:
NA.47
PubChem Substance ID:
UNSPSC Code:
12171500
EC Number:
249-431-8
MDL number:
form
powder, crystals or chunks
Quality Level
mp
70-72 °C (lit.)
application(s)
diagnostic assay manufacturing
hematology
histology
storage temp.
room temp
SMILES string
CC(C)C1=C(Br)C(=O)C(C)=C(Br)C1=O
InChI
1S/C10H10Br2O2/c1-4(2)6-8(12)9(13)5(3)7(11)10(6)14/h4H,1-3H3
InChI key
GHHZELQYJPWSMG-UHFFFAOYSA-N
Application
2, 5-Dibromo-6-isopropyl-3-methyl-1, 4-benzoquinone has been used as a metabolic inhibitor of violaxanthin (V) cycle of Pelvetia canaliculata and is used as a photosynthetic electron transport chain (pETC) inhibitor.
Biochem/physiol Actions
2, 5-Dibromo-6-isopropyl-3-methyl-1, 4-benzoquinone acts as an inhibitor of respiratory and photosynthetic processes.
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
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Activation of violaxanthin cycle in darkness is a common response to different abiotic stresses: a case study in Pelvetia canaliculata
Marin BF<
BMC plant biology (2011)
Gert Schansker et al.
Biochimica et biophysica acta, 1706(3), 250-261 (2005-02-08)
The effects of dibromothymoquinone (DBMIB) and methylviologen (MV) on the Chl a fluorescence induction transient (OJIP) were studied in vivo. Simultaneously measured 820-nm transmission kinetics were used to monitor electron flow through photosystem I (PSI). DBMIB inhibits the reoxidation of
Chloroplasts extend stromules independently and in response to internal redox signals
Brunkard J O, et.al.
Proceedings of the National Academy of Sciences of the USA, 112, 10044-10049 (2015)
Global Trade Item Number
| SKU | GTIN |
|---|---|
| 271993-250MG | 04061826143988 |