Cart
sales@molnova.com
Dichlorisone Acetate
CAS No. 79-61-8
Dichlorisone Acetate( Dichlorisone acetate )
Catalog No. M15983 CAS No. 79-61-8
It belongs to organophosphate compounds, used as a kind of common environmental health insecticide.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 1 mL x 10 mM in DMSO | 51 | In Stock |
|
| 5MG | 38 | In Stock |
|
| 10MG | 61 | In Stock |
|
| 25MG | 103 | In Stock |
|
| 50MG | 152 | In Stock |
|
| 100MG | 226 | In Stock |
|
| 200MG | 334 | In Stock |
|
| 500MG | Get Quote | In Stock |
|
| 1G | Get Quote | In Stock |
|
Biological Information
-
Product NameDichlorisone Acetate
-
NoteResearch use only, not for human use.
-
Brief DescriptionIt belongs to organophosphate compounds, used as a kind of common environmental health insecticide.
-
DescriptionIt belongs to organophosphate compounds, used as a kind of common environmental health insecticide.
-
In Vitro——
-
In Vivo——
-
SynonymsDichlorisone acetate
-
PathwayEndocrinology/Hormones
-
TargetAChR
-
RecptorAChE
-
Research Area——
-
Indication——
Chemical Information
-
CAS Number79-61-8
-
Formula Weight455.4
-
Molecular FormulaC23H28Cl2O5
-
Purity>98% (HPLC)
-
SolubilityDMSO: 10 mM
-
SMILESC[C@@]12[C@](C(COC(C)=O)=O)(O)CC[C@@]1([H])[C@]3([H])CCC4=CC(C=C[C@]4(C)[C@@]3(Cl)[C@@H](Cl)C2)=O
-
Chemical Name(11beta)-21-(Acetyloxy)-9,11-dichloro-17-hydroxypregna-1,4-diene-3,20-dione
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
Stability≥ 2 years
Reference
1. JEANDIDIER P. Ann Med Nancy. 1964 Aug-Sep;42:1062-5.
molnova catalog
related products
-
2-Pyridinealdoxime m...
Pralidoxime chloride is a useful agent in the treatment of organophosphate poisoning.
-
PSEM 89S TFA
PSEM 89S TFA is a brain-penetrant and selective ion channels agonist, and is orthogonally selective for Q79G and L141F, respectively.
-
Nicotine Ditartrate
(?)-Nicotine is the dominant form of the natural alkaloid nicotine. It acts as an agonist of neuronal nicotinic acetylcholine receptors (nAChRs) and possesses addictive and teratogenic properties. (?)-(S)-Nicotine is significantly more active at binding nAChRs compared to the (+)-(R) antipode thus nicotine is typically synthesized as (?)-(S)-nicotine with only 0.2-1% of the (+)-(R) isomer present.
