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Hubei Langyou International Trading Co., Ltd99%min Ampicillin 69-53-4 For Antibiotic//file1.lookchem.com/cas/reactions/2021/06/01/4300240.png
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99%min Ampicillin 69-53-4 For Antibiotic CAS NO.69-53-4

Min.Order Quantity:
10 Gram
Purity:
99%min
Port:
ShangHai
Payment Terms:
T/T,MoneyGram

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Product Details

Keywords

  • 99%min Ampicillin
  • Ampicillin Manufacturer
  • For Antibiotic,Broad-spectrum Penicillin

Quick Details

  • ProName: 99%min Ampicillin 69-53-4 For Antibiot...
  • CasNo: 69-53-4
  • Molecular Formula: C16H19N3O4S
  • Appearance: White Powder
  • Application: For Pharmaceutical Raw Materials
  • DeliveryTime: 2-4 days after confirmed your payments
  • PackAge: 100g/ bag, 2 kg/ bag, 25kg/ carton or ...
  • Port: ShangHai
  • ProductionCapacity: 1000 Metric Ton/Month
  • Purity: 99%min
  • Storage: Dry and cool place
  • Transportation: By DHL, TNT, FedEx, HKEMS, UPS, Etc
  • LimitNum: 10 Gram

Superiority

advantages:

hubei xinrunde chemical co., ltd is a renowned pharmaceutical manufacturer. we can offer high quality products at competitive price in quick delivery with 100% custom pass guaranteed. never stop striving to offer our best service is our philosophy. we have flexible and untraceable payment terms. as a leading manufacture, our products have been exported to germany, norway, poland, finland, spain, uk, france, russia, usa, brazil, mexico, australia, japan, korea, thailand, indonesia, uruguay and many other countries.


1. quality.every batch of steroid powders have tobetested by our qc(quality control) before they are allowed to sell.


2 . delivery we have stock, so we can delivery quickly at the very day when receive the payment. within 24 hours after receiving the payment lead time 4 or 7 days.


3 . discreet package safelyand professionally disguised package guaranteed. for your safety and to insure delivery all products will be packed in a discreet way to prevent any suspicions, no steroids related name will appear on the parcels. high successful delivery rate

4 . warm after-sale service any of your question would be solved for the first as soon as possible.

Details

ampicillin basic information
product name: ampicillin
synonyms: 6-[d-alpha-aminophenylacetamido]penicillanic acid trihydrate;alpha-aminobenzylpenicillin, trihydrate;d(-)-alpha-aminobenzylpenicillin;d(-)-alpha-aminobenzylpenicillin trihydrate;(aminophenylmethyl)-penicilli;[2s-[2alpha,5alpha,6beta(s)]]-o]-3-dimethyl-7-oxo;4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylicacid,6-[(aminophenylacetyl)amin;6-(d(-)-alpha-aminophenylacetamido)penicillanicacid
cas: 69-53-4
mf: c16h19n3o4s
mw: 349.41
einecs: 200-709-7
product categories: chiral reagents;intermediates & fine chemicals;isotope labeled compounds;pharmaceuticals;veterinary medicine,soluble powder;isotope labelled compounds;sulfur & selenium compounds;antibacterial drugs;thiazines ,thiazoles;api
mol file: 69-53-4.mol
ampicillin structure
ampicillin chemical properties
melting point 198-200 °c (dec.)(lit.)
alpha d23 +287.9° (c = 1 in water)
storage temp. 2-8°c
solubility nh4oh 1 m: 50 mg/ml, clear, colorless
pka 2.5 (cooh)(at 25℃)
merck 13,591
stability: stable, but may be moisture sensitive. incopmpatible with strong oxidizing agents.
cas database reference 69-53-4(cas database reference)
epa substance registry system 4-thia-1-azabicyclo[ 3.2.0]heptane-2-carboxylic acid, 6-[[(2r)-aminophenylacetyl] amino]-3,3-dimethyl-7-oxo-, (2s,5r,6r)-(69-53-4)
safety information
hazard codes xn,t
risk statements 36/37/38-42/43-61
safety statements 22-26-36/37-45-53
wgk germany 2
rtecs xh8425000
f 10-23
hs code 29212900
hazardous substances data 69-53-4(hazardous substances data)
ampicillin usage and synthesis
description ampicillin is an antibacterial antibiotic from the α-aminobenzyl penicillin group, which differs from penicillin by the presence of an amino group that facilitates penetration through the outer membrane of some gram-negative bacteria.
ampicillin is semi-synthetic derivative of penicillin that functions as an orally active broad-spectrum antibiotic. ampicillin acts by interfering directly with the biosynthesis of peptidoglycan, which constitutes the major component of the bacterial cell wall, leading to structural instability and death of bacteria.
ampicillin is a β-lactam antibiotic within the penicillin family. as a member of this family, ampicillin is susceptible to β-lactamase, which hydrolyzes the β-lactam ring. this broad spectrum antibiotic is effective against gram-positive, gram-negative bacteria and anaerobic bacteria. ampicillin is widely used in cell culture as a selective agent. as an antibiotic, ampicillin binds to penicillin binding proteins (pbps) on a susceptible organism and inhibits bacterial cell-wall synthesis by inactivating transpeptidases on the inner surface of the bacterial cell membrane. after binding to the pbps, ampicilin acts as a structural analogue of acyl-d-alanyl-d-alanine, acylates the transpeptidase enzyme and thereby prevents the cross-linking of the peptidoglycan of the cell wall necessary for the growth of the bacterium.
ampicillin sodium can be used as a selective agent in several types of isolation media. ampicillin sodium is routinely used to select for cells containing the pcdna3.1 and peak10 resistance plasmids in cell line a904l at an effective concentration of 50 μg/ml.
chemical properties crystalline solid
uses β-lactam antibiotics
uses labelled ampicillin. orally active, semi-synthetic antibiotic; structurally related to penicillin. antibacterial.
definition chebi: a penicillin in which the substituent at position 6 of the penam ring is a 2-amino-2-phenylacetamido group.

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