text.skipToContent text.skipToNavigation

Maximum quantity allowed is 999

Please select the quantity

CAS RN: 39831-55-5 | Product Number: A2281

Amikacin Sulfate


Purity: >98.0%(HPLC)
Synonyms:
  • Amikacin Disulfate
  • O-3-Amino-3-deoxy-α-D-glucopyranosyl-(1→6)O-[6-amino-6-deoxy-α-D-glucopyranosyl-(1→4)]-N1-[(2S)-4-amino-2-hydroxy-1-oxobutyl]-2-deoxy-D-streptamine Sulfate
Product Documents:
5G
A$119.00
34   15   It can be shipped in about 2 weeks after ordering
25G
A$329.00
1   12   It can be shipped in about 2 weeks after ordering
* Please contact our distributor of Chem-Supply if you would like to purchase TCI products. The above prices do not include freight cost, customs charge and other charges to the destination.
* ChemSupply Australia Pty Ltd (Phone: 08-8440-2000 / email:  sales@chemsupply.com.au)

Product Number A2281
Purity / Analysis Method >98.0%(HPLC)
Molecular Formula / Molecular Weight C__2__2H__4__3N__5O__1__3·2H__2SO__4 = 781.75 
Physical State (20 deg.C) Solid
Storage Temperature Refrigerated (0-10°C)
Store Under Inert Gas Store under inert gas
Condition to Avoid Hygroscopic,Heat Sensitive
CAS RN 39831-55-5
Reaxys Registry Number 6172633
PubChem Substance ID 468590111
Merck Index (14) 405
MDL Number

MFCD00167475

Specifications
Appearance White to Light yellow powder to crystal
Purity(HPLC)(CAD) min. 98.0 area%
Specific rotation +76.0 to +84.0 deg(C=1, water)(calcd.on anh.substance)
Water max. 13.0 %
Properties (reference)
Melting Point 230 °C(dec.)
GHS
Related Laws:
RTECS# WK1961200
Transport Information:
H.S.code* 2941.90-000
*This code is applied to the products when TCI exports from Japan and not for import in your country.
Application
Amikacin sulfate: A Polycationic Bactericidal Aminoglycoside

Amikacin sulfate is a polycationic, semisynthetic, bactericidal aminoglycoside. Amikacin was synthesized by acylation with the L-(-)-γ-amino-α-hydroxybutyryl side chain at the C-1 amino group of the deoxystreptamine moiety of kanamycin [K0047]. Amikacin is very active against most Gram-negative bacteria including gentamicin- [G0383] and tobramycin- [T2503] resistant strains. Amikacin enters the bacterial cell by binding to negatively charged components of the bacterial cell wall disrupting the overall architecture of the cell wall. The mechanism of action is disruption and inhibition of protein synthesis in the target bacteria by binding to the 30S ribosomal subunit.1,2) In addition, amikacin is devoid of any chromophore and/or conjugated system prerequisite for UV and florescent light detection (FLD). Hence, simple and sensitive liquid chromatography methods have been developed for the determination of amikacin.3-5) (The product is for research purpose only.)

References


Product Documents (Note: Some products will not have analytical charts available.)
Safety Data Sheet (SDS)
Please select Language.

The requested SDS is not available.

Please Contact Us for more information.

Specifications
C of A & Other Certificates
Please enter Lot Number Incorrect Lot Number. Please input only the 4-5 alphanumeric characters before the hyphen.

The product with the lot number searched for has been discontinued and no related documentation is available.

Sample C of A
This is a sample C of A and may not represent a recently manufactured lot of the product.

A sample C of A for this product is not available at this time.

Analytical Charts
Please enter Lot Number Incorrect Lot Number. Please input only the 4-5 alphanumeric characters before the hyphen.

The requested analytical chart is not available. Sorry for the inconvenience.

The product with the lot number searched for has been discontinued and no related documentation is available.

Other Documents

Session Status
Your session will timeout in 10 minutes. You will be redirected to the HOME page after session timeout. Please click the button to continue session from the same page. minute. You will be redirected to the HOME page after session timeout. Please click the button to continue session from the same page.

Your session has timed out. You will be redirected to the HOME page.