Formaldehyde+sodium+bisulfite
Supplier:
AMBEED, INC
Description:
Sodium 3-[(3,5-Dimethoxyphenyl)(ethyl)amino]-2-hydroxypropane-1-sulfonate, Purity: 95%, CAS Number: 83777-30-4, Appearance: Form: solid, Storage: Inert atmosphere, Room Temperature, Size: 1mg
Supplier:
Thermo Scientific Chemicals
Description:
MDL: MFCD00011118
Notes: Decomposes above 320°C
Soluble in water
Fieser: 1,1097 11,491 13,282 16,308 18,336 19,313 20,350 21,405
Supplier:
TCI America
Description:
CAS Number: 7423-32-7
MDL Number: MFCD00058971 Form: Crystal Color: White
Supplier:
Thermo Scientific Chemicals
Description:
Inhibits CD45 protein tyrosine phosphatase and farnesyl diphosphate synthase; induces apoptosis
Supplier:
Ricca Chemical
Description:
0.04% (w/v) Aqueous. pH 1.2 (red) - 2.8-7.4 (yellow) - 9.0 (purple). Container: Plastic.
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Supplier:
Matrix Scientific
Description:
MF=C15H12NNAO3 MW=277.26 CAS=61941-56-8 MDL=MFCD09842317 1G
Catalog Number:
(101874-966)
Supplier:
Matrix Scientific
Description:
Matrix Scientific Part Number: 046290-500MG , MDL Number: MFCD01075150
Supplier:
TCI America
Description:
CAS Number: 1070-89-9
MDL Number: MFCD00009835 Molecular Formula: C6H19NSi2 Molecular Weight: 183.38 Form: Clear Liquid Color: Yellow Flash Point (°C): -22
Supplier:
Ricca Chemical
Description:
Sodium Standard Stock Solution, 2000 ppm Na, Ricca Chemical Company
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Catalog Number:
(100504-278)
Supplier:
Electron Microscopy Sciences
Description:
Granular, Reagent Na3C6H5O7·2H2O F.W. 294.11 CAS #6132-04-3 Assay - 0.999 Insoluble Matters - 0.00005 Free Acid (as Citric) - 0.0002 Free Alkali - 0.0005 Chloride - 0.00003 Sulfate - 0.00005 Calcium - 0.00005 Heavy Metals - .3ppm Iron
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Supplier:
Thermo Scientific Chemicals
Description:
MDL: MFCD00077263
Notes: Transition interval: pH 6.0 (yellow) to pH 7.6 (blue)
Supplier:
MP Biomedicals
Description:
Cefotaxime is a cephalosporin, which acts by interference of synthesis of peptidoglycan of the bacterial cell wall. Cefotaxime, a cephalosporin antibiotic, is active against both gram-negative and gram-positive bacteria. In addition, cefotaxime blocks the division of cyanobacteria and lower plant organelles/plastids such as the photosynthetic organelles of Glaucophytes and chloroplasts of bryophytes.
Cefotaxime is used for infections of the respiratory tract, skin, bones, joints, urogenital system, meninges, and bloodstream. It generally has good coverage against most Gram-negative bacteria, with the notable exception of Pseudomonas. It is also effective against most Gram-positive cocci except for Enterococcus. It is active against penicillin-resistant strains of Streptococcus pneumoniae. It has modest activity against the anaerobic Bacteroides fragilis. In meningitis, cefotaxime crosses the blood–brain barrier better than cefuroxime. Cefotaxim inhibits bacterial cell wall synthesis by binding to penicillin-binding proteins (PBPs) which inhibits the final transpeptidation step of peptidoglycan synthesis in bacterial cell walls. As a result, bacteria lyse due to cell wall autolytic enzymes.
Catalog Number:
(68000-322)
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