Dicloxacillin sodium salt monohydrate
Manufacturer: Sigma Aldrich
CAS Number: 13412-64-1
Synonym(S): 3-(2,6-Dichlorophenyl)-5-methyl-4-isoxazolyl penicillin sodium salt monohydrate
Select a Size
| Pack Size | SKU | Availability | Price |
|---|---|---|---|
| 1 G | D9016-1-G | In Stock | ₹ 9,287.85 |
D9016 - 1 G
In Stock
Quantity
1
Base Price: ₹ 9,287.85
GST (18%): ₹ 1,671.813
Total Price: ₹ 10,959.663
form
powder or crystals
Quality Level
200
color
white to off-white
solubility
H2O: 100 mg/mL
antibiotic activity spectrum
Gram-negative bacteriaGram-positive bacteria
Mode of action
cell wall synthesis | interferes
storage temp.
2-8°C
SMILES string
O.[Na+].Cc1onc(c1C(=O)N[C@H]2[C@H]3SC(C)(C)[C@@H](N3C2=O)C([O-])=O)-c4c(Cl)cccc4Cl
InChI
1S/C19H17Cl2N3O5S.Na.H2O/c1-7-10(12(23-29-7)11-8(20)5-4-6-9(11)21)15(25)22-13-16(26)24-14(18(27)28)19(2,3)30-17(13)24;;/h4-6,13-14,17H,1-3H3,(H,22,25)(H,27,28);;1H2/q;+1;/p-1/t13-,14+,17-;;/m1../s1
InChI key
SIGZQNJITOWQEF-VICXVTCVSA-M
Other Options
| Image | Product Name | Manufacturer | Price Range | |
|---|---|---|---|---|
 | Dicloxacillin Sodium, British Pharmacopoeia (BP) Reference Standard, MilliporeSigma™ Supelco™ | MilliporeSigma Supelco | ₹ 26,865.84 | |
 | VETRANAL™ Dicloxacillin sodium salt hydrate, MilliporeSigma™ Supelco™ | MilliporeSigma Supelco | ₹ 6,181.71 | |
 | Dicloxacillin sodium salt hydrate | Supelco | ₹ 6,224.38 | |
 | Dicloxacillin sodium | Sigma Aldrich | ₹ 40,756.13 | |
| | Dicloxacillin sodium | Sigma Aldrich | ₹ 14,267.35 | |
| | Dicloxacillin sodium | Sigma Aldrich | ₹ 24,767.60 | |
| | Dicloxacillin sodium salt monohydrate | Sigma Aldrich | ₹ 9,287.85 | |
 | 13412-64-1 | Dicloxacillin Sodium Salt Monohydrate | A2B Chem | ₹ 1,112.28 - ₹ 55,015.08 |
Related Products
Description
- General description: Chemical structure: ß-lactam
- Application: Dicloxacillin is a β-lactamase resistant penicillin similar to oxacillin. Dicloxacillin has in vitro activity against gram-positive and gram-negative aerobic and anaerobic bacteria. It is resistant to penicillinase. It is used to study bacterial cell wall biosynthesis at the level of peptidogylcan cross-linking and to study mechanisms of penicillinase (β-lactamase) resistance. It is used to study phenylbutazone plasma binding[1] and extracellular and intracellular killing of Staphylococcus aureus[2]
- Biochem/physiol Actions: Docloxacillin binds to specific penicillin-binding proteins (PBPs) in the bacterial cell wall and therefore inhibits the last stage of bacterial cell wall synthesis. Cell lysis, mediated by bacterial cell wall autolytic enzymes, is the result. Dicloxacillin may interfere with autolysin inhibitors .
SAFETY INFORMATION
Pictograms
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Irrit. 2 - Resp. Sens. 1 - Skin Irrit. 2 - STOT SE 3
Target Organs
Respiratory system
WGK
WGK 2
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Compare Similar Items
Show Difference
form: powder or crystals
Quality Level: 200
color: white to off-white
solubility: H2O: 100 mg/mL
antibiotic activity spectrum: Gram-negative bacteriaGram-positive bacteria
Mode of action: cell wall synthesis | interferes
storage temp.: 2-8°C
SMILES string: O.[Na+].Cc1onc(c1C(=O)N[C@H]2[C@H]3SC(C)(C)[C@@H](N3C2=O)C([O-])=O)-c4c(Cl)cccc4Cl
InChI: 1S/C19H17Cl2N3O5S.Na.H2O/c1-7-10(12(23-29-7)11-8(20)5-4-6-9(11)21)15(25)22-13-16(26)24-14(18(27)28)19(2,3)30-17(13)24;;/h4-6,13-14,17H,1-3H3,(H,22,25)(H,27,28);;1H2/q;+1;/p-1/t13-,14+,17-;;/m1../s1
InChI key: SIGZQNJITOWQEF-VICXVTCVSA-M
form: __
Quality Level: 100
color: __
solubility: __
antibiotic activity spectrum: __
Mode of action: __
storage temp.: room temp
SMILES string: __
InChI: __
InChI key: __
form: __
Quality Level: 100
color: __
solubility: __
antibiotic activity spectrum: __
Mode of action: __
storage temp.: room temp
SMILES string: __
InChI: __
InChI key: __
