P8396
Piperacillin sodium salt
penicillin analog
Manufacturer: Sigma Aldrich
CAS Number: 59703-84-3
Select a Size
| Pack Size | SKU | Availability | Price |
|---|---|---|---|
| 1 G | P8396-1-G | In Stock | ₹ 10,770.88 |
| 5 G | P8396-5-G | In Stock | ₹ 28,480.58 |
| 10 G | P8396-10-G | In Stock | ₹ 59,288.53 |
P8396 - 1 G
In Stock
Quantity
1
Base Price: ₹ 10,770.88
GST (18%): ₹ 1,938.758
Total Price: ₹ 12,709.638
Quality Level
200
form
powder
solubility
H2O: soluble 50 mg/mL
antibiotic activity spectrum
Gram-negative bacteriaGram-positive bacteria
Mode of action
cell wall synthesis | interferes
storage temp.
2-8°C
SMILES string
[Na+].CCN1CCN(C(=O)N[C@@H](C(=O)N[C@H]2[C@H]3SC(C)(C)[C@@H](N3C2=O)C([O-])=O)c4ccccc4)C(=O)C1=O
InChI
1S/C23H27N5O7S.Na/c1-4-26-10-11-27(19(32)18(26)31)22(35)25-13(12-8-6-5-7-9-12)16(29)24-14-17(30)28-15(21(33)34)23(2,3)36-20(14)28;/h5-9,13-15,20H,4,10-11H2,1-3H3,(H,24,29)(H,25,35)(H,33,34);/q;+1/p-1/t13-,14-,15+,20-;/m1./s1
InChI key
WCMIIGXFCMNQDS-IDYPWDAWSA-M
Other Options
| Image | Product Name | Manufacturer | Price Range | |
|---|---|---|---|---|
 | Piperacillin sodium salt, MilliporeSigma™ Supelco™ | MilliporeSigma Supelco | ₹ 11,858.62 | |
 | Sigma Aldrich Fine Chemicals Biosciences Piperacillin sodium salt penicillin analog | 59703-84-3 | MFCD00917471 | 5G | Sigma Aldrich Fine Chemicals Biosciences | ₹ 45,175.68 | |
 | Sigma Aldrich Fine Chemicals Biosciences Piperacillin sodium salt penicillin analog | 59703-84-3 | MFCD00917471 | 10G | Sigma Aldrich Fine Chemicals Biosciences | ₹ 66,028.36 | |
 | Piperacillin sodium salt | Supelco | ₹ 9,461.05 | |
| | Piperacillin sodium salt | Sigma Aldrich | ₹ 10,770.88 - ₹ 59,288.53 | |
 | 4-Thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid, 6-[[(2R)-2-[[(4-ethyl-2,3-dioxo-1-piperazinyl)carbonyl]amino]-2-phenylacetyl]amino]-3,3-dimethyl-7-oxo-, sodium salt (1:1), (2S,5R,6R)- | Aaron Chemicals LLC | ₹ 598.92 - ₹ 61,774.32 |
Related Products
Description
- General description: Chemical structure: ß-lactam
- Application: Piperacillin is a semisynthetic, broad-spectrum ureidopenicillin antibiotic. It is derived from ampicillin. It has been used in pharmacokinetic studies in order to optimize antimicrobial therapy in patients with sepsis[1]. It is used to study piperacillin hypersensitivity reactions[2] and to study multidrug-resistant organisms[3].
- Biochem/physiol Actions: Piperacillin inhibits the last stage of bacterial cell wall synthesis by binding to certain penicillin-binding proteins (PBPs), which results in cell lysis. Cell lysis is mediated by bacterial cell wall autolytic enzymes. Piperacillin may interfere with autolysin inhibitors.
- Packaging: 1g,5g,10g
- Other Notes: Keep container tightly closed in a dry and well-ventilated place.Keep in a dry place.
SAFETY INFORMATION
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
Quality Level: 200
form: powder
solubility: H2O: soluble 50 mg/mL
antibiotic activity spectrum: Gram-negative bacteriaGram-positive bacteria
Mode of action: cell wall synthesis | interferes
storage temp.: 2-8°C
SMILES string: [Na+].CCN1CCN(C(=O)N[C@@H](C(=O)N[C@H]2[C@H]3SC(C)(C)[C@@H](N3C2=O)C([O-])=O)c4ccccc4)C(=O)C1=O
InChI: 1S/C23H27N5O7S.Na/c1-4-26-10-11-27(19(32)18(26)31)22(35)25-13(12-8-6-5-7-9-12)16(29)24-14-17(30)28-15(21(33)34)23(2,3)36-20(14)28;/h5-9,13-15,20H,4,10-11H2,1-3H3,(H,24,29)(H,25,35)(H,33,34);/q;+1/p-1/t13-,14-,15+,20-;/m1./s1
InChI key: WCMIIGXFCMNQDS-IDYPWDAWSA-M
Quality Level:
200
form:
powder
solubility:
H2O: soluble 50 mg/mL
antibiotic activity spectrum:
Gram-negative bacteriaGram-positive bacteria
Mode of action:
cell wall synthesis | interferes
storage temp.:
2-8°C
SMILES string:
[Na+].CCN1CCN(C(=O)N[C@@H](C(=O)N[C@H]2[C@H]3SC(C)(C)[C@@H](N3C2=O)C([O-])=O)c4ccccc4)C(=O)C1=O
InChI:
1S/C23H27N5O7S.Na/c1-4-26-10-11-27(19(32)18(26)31)22(35)25-13(12-8-6-5-7-9-12)16(29)24-14-17(30)28-15(21(33)34)23(2,3)36-20(14)28;/h5-9,13-15,20H,4,10-11H2,1-3H3,(H,24,29)(H,25,35)(H,33,34);/q;+1/p-1/t13-,14-,15+,20-;/m1./s1
InChI key:
WCMIIGXFCMNQDS-IDYPWDAWSA-M
Quality Level: 200
form: tablet
solubility: water: 1 tablet/10 mL, clear, colorless
antibiotic activity spectrum: __
Mode of action: __
storage temp.: 2-8°C
SMILES string: Cl[H].Cl[H].Nc1ccccc1N
InChI: 1S/C6H8N2.2ClH/c7-5-3-1-2-4-6(5)8;;/h1-4H,7-8H2;2*1H
InChI key: RIIWUGSYXOBDMC-UHFFFAOYSA-N
Quality Level:
200
form:
tablet
solubility:
water: 1 tablet/10 mL, clear, colorless
antibiotic activity spectrum:
__
Mode of action:
__
storage temp.:
2-8°C
SMILES string:
Cl[H].Cl[H].Nc1ccccc1N
InChI:
1S/C6H8N2.2ClH/c7-5-3-1-2-4-6(5)8;;/h1-4H,7-8H2;2*1H
InChI key:
RIIWUGSYXOBDMC-UHFFFAOYSA-N
Quality Level: 200
form: essentially salt-free, lyophilized powder
solubility: 0.1 M phosphate buffer: soluble (pH 6.0)H2O: soluble
antibiotic activity spectrum: __
Mode of action: __
storage temp.: 2-8°C
SMILES string: __
InChI: 1S/H2O3/c1-3-2/h1-2H
InChI key: JSPLKZUTYZBBKA-UHFFFAOYSA-N
Quality Level:
200
form:
essentially salt-free, lyophilized powder
solubility:
0.1 M phosphate buffer: soluble (pH 6.0)H2O: soluble
antibiotic activity spectrum:
__
Mode of action:
__
storage temp.:
2-8°C
SMILES string:
__
InChI:
1S/H2O3/c1-3-2/h1-2H
InChI key:
JSPLKZUTYZBBKA-UHFFFAOYSA-N
Quality Level: 500
form: liquid
solubility: __
antibiotic activity spectrum: __
Mode of action: __
storage temp.: 2-8°C
SMILES string: __
InChI: __
InChI key: __
Quality Level:
500
form:
liquid
solubility:
__
antibiotic activity spectrum:
__
Mode of action:
__
storage temp.:
2-8°C
SMILES string:
__
InChI:
__
InChI key:
__