logo
Send Message
Hefei Home Sunshine Pharmaceutical Technology Co.,Ltd
products
products
Home > products > Pharmaceutical Intermediates > Cemandil Sodium Salt CAS 42540-40-9

Cemandil Sodium Salt CAS 42540-40-9

Product Details

Place of Origin: China

Brand Name: Sunshine

Certification: ISO,COA

Model Number: 42540-40-9

Payment & Shipping Terms

Minimum Order Quantity: Negotiation

Price: Negotiation

Packaging Details: Aluminum Foil Bag, Drum

Delivery Time: 7-15DAY

Payment Terms: L/C,D/A,D/P,T/T,Western Union,MoneyGram

Supply Ability: G,KG,TON

Get Best Price
Highlight:
CAS NO::
42540-40-9
Appearance::
White Solid
Molecular Formula::
C19H17N6NaO6S2
Molecular Weight::
512.49500
EINECS NO::
255-877-4
MDL NO::
MFCD00864877
CAS NO::
42540-40-9
Appearance::
White Solid
Molecular Formula::
C19H17N6NaO6S2
Molecular Weight::
512.49500
EINECS NO::
255-877-4
MDL NO::
MFCD00864877
Cemandil Sodium Salt CAS 42540-40-9

Product Description:

Product Name: Cemandil sodium salt CAS NO: 42540-40-9


Synonyms:

Cefamandole formate sodium salt;

CefamandoleNafate;

Cemandil sodium salt;


Chemical & Physical Properties:

Appearance: White solid

Assay :≥99.00%

Melting Point: 190-193℃

Storage Condition: -20℃ Freezer, Under Inert Atmosphere


Safety Information:

Safety Statements: S26; S36

HS Code: 3003201900

Risk Statements: R36/37/38; R42/43

Hazard Code: Xn

WGK Germany: 3


Cefamandole (INN, also known as cephamandole) is a second-generation broad-spectrum cephalosporin antibiotic. The clinically used form of cefamandole is the formate ester cefamandole nafate, a prodrug which is administered parenterally. Cefamandole is no longer available in the United States.

The chemical structure of cefamandole, like that of several other cephalosporins, contains an N-methylthiotetrazole (NMTT or 1-MTT) side chain. As the antibiotic is broken down in the body, it releases free NMTT, which can cause hypoprothrombinemia (likely due to inhibition of the enzyme vitamin K epoxide reductase)(vitamin K supplement is recommended during therapy) and a reaction with ethanol similar to that produced by disulfiram (Antabuse), due to inhibition of aldehyde dehydrogenase.

Cefamandole has a broad spectrum of activity and can be used to treat bacterial infections of the skin, bones and joints, urinary tract, and lower respiratory tract. The following represents cefamandole MIC susceptibility data for a few medically significant microorganisms.

Escherichia coli: 0.12 - 400 μg/ml Haemophilus influenzae: 0.06 - >16 μg/ml Staphylococcus aureus: 0.1 - 12.5 μg/ml; ; CO2 is generated during the normal constitution of cefamandole and ceftazidime, potentially resulting in an explosive-like reaction in syringes.


If you are interested in our products or have any questions, please feel free to contact us!


Products under patent are offered for R & D purpose only. However, the final responsibility lies exclusively with the buyer.