A6140

Ampicillin trihydrate

900-1050 μg/mg anhydrous basis (HPLC)

Manufacturer: Sigma Aldrich

CAS Number: 7177-48-2

Synonym(S): α-Aminobenzylpenicillin trihydrate, Aminobenzyl Penicillin, Ampicillin, D-(−)-α-Aminobenzylpenicillin

Select a Size

Pack Size SKU Availability Price
5 G A6140-5-G In Stock ₹ 6,246.03
25 G A6140-25-G In Stock ₹ 14,083.33
100 G A6140-100-G In Stock ₹ 25,114.00

A6140 - 5 G

₹ 6,246.03

In Stock

Quantity

1

Base Price: ₹ 6,246.03

GST (18%): ₹ 1,124.285

Total Price: ₹ 7,370.315

Quality Level

200

form

powder or crystals

concentration

900-1050 μg/mg (anhydrous, HPLC)

mp

198-200 °C (dec.) (lit.)

antibiotic activity spectrum

Gram-negative bacteriaGram-positive bacteria

Mode of action

cell wall synthesis | interferes

storage temp.

2-8°C

SMILES string

O.O.O.CC1(C)S[C@@H]2[C@H](NC(=O)[C@H](N)c3ccccc3)C(=O)N2[C@H]1C(O)=O

InChI

1S/C16H19N3O4S.3H2O/c1-16(2)11(15(22)23)19-13(21)10(14(19)24-16)18-12(20)9(17)8-6-4-3-5-7-8;;;/h3-7,9-11,14H,17H2,1-2H3,(H,18,20)(H,22,23);3*1H2/t9-,10-,11+,14-;;;/m1.../s1

InChI key

RXDALBZNGVATNY-CWLIKTDRSA-N

Other Options

Image Product Name Manufacturer Price Range
50-199-8630
Apexbio Technology LLC Ampicillin Trihydrate, 1g Cas# 7177-48-2
Apexbio Technology LLC ₹ 4,534.68
31591
Ampicillin trihydrate
Supelco ₹ 6,062.00
1033407
Ampicillin trihydrate
Sigma Aldrich ₹ 40,756.13
A1100000
Ampicillin trihydrate
Sigma Aldrich ₹ 14,267.35
BP021
Ampicillin trihydrate
Sigma Aldrich ₹ 20,794.83
A1593
Ampicillin
Sigma Aldrich ₹ 26,120.73
A1593
Ampicillin
Sigma Aldrich ₹ 26,120.73
A6140
Ampicillin trihydrate
Sigma Aldrich ₹ 6,246.03 - ₹ 25,114.00
CS-0013100
Ampicillin (trihydrate)
ChemScene ₹ 4,363.56 - ₹ 11,293.92

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Description

  • General description: Chemical structure: ß-lactam
  • Application: Ampicillin Trihydrate is commonly used to select for ampicillin resistance in mutated and transformed cells.
  • Biochem/physiol Actions: A β-lactam antibiotic with an amino group side chain attached to the penicillin structure. Penicillin derivative that inhibits bacterial cell-wall synthesis (peptidoglycan cross-linking) by inactivating transpeptidases on the inner surface of the bacterial cell membrane. Bactericidal only to growing Escherichia coli . Mode of resistance: Cleavage of β-lactam ring of ampicillin by β-lactamase. Antimicrobial spectrum: Gram-negative and Gram-positive bacteria.
  • Other Notes: Keep container tightly closed in a dry and well-ventilated place.

SAFETY INFORMATION

Pictograms

GHS08,GHS07

Signal Word

Danger

Hazard Statements

H315,H317,H319,H334,H335

Precautionary Statements

P261 - P264 - P271 - P280 - P302 + P352 - P305 + P351 + P338

Hazard Classifications

Eye Irrit. 2 - Resp. Sens. 1 - Skin Irrit. 2 - Skin Sens. 1 - 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

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Sigma Aldrich

A6140

900-1050 μg/mg anhydrous basis (HPL...


Quality Level:
200

form:
powder or crystals

concentration:
900-1050 μg/mg (anhydrous, HPLC)

mp:
198-200 °C (dec.) (lit.)

antibiotic activity spectrum:
Gram-negative bacteriaGram-positive bacteria

Mode of action:
cell wall synthesis | interferes

storage temp.:
2-8°C

SMILES string:
O.O.O.CC1(C)S[C@@H]2[C@H](NC(=O)[C@H](N)c3ccccc3)C(=O)N2[C@H]1C(O)=O

InChI:
1S/C16H19N3O4S.3H2O/c1-16(2)11(15(22)23)19-13(21)10(14(19)24-16)18-12(20)9(17)8-6-4-3-5-7-8;;;/h3-7,9-11,14H,17H2,1-2H3,(H,18,20)(H,22,23);3*1H2/t9-,10-,11+,14-;;;/m1.../s1

InChI key:
RXDALBZNGVATNY-CWLIKTDRSA-N

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ATRRKUHOCOJYRX-UHFFFAOYSA-N

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ATRRKUHOCOJYRX-UHFFFAOYSA-N

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