6-(2-Methylpropoxy)pyridine-3-boronic+acid
Catalog Number:
(ALA151515-5G)
Supplier:
ALADDIN SCIENTIFIC
Description:
3-Amino-5-phenylpyrazole ((3-phenyl-1H-pyrazol-5-amine) may be used in the synthesis of the following: · Urea derivatives by reaction with azido(6-(benzofuran-2-yl)-2-methylpyridin-3-yl) methanone. · 2-Mercaptoacetamide analogs by treating with thioglycolic acid. · 3-(Substituentpyrimidayl)-5,6-benzocoumarins by treating with 3-(2′-formyl-1′-chlorovinyl)-5,6-benzocoumarin. · Substituted 2,7-diphenylpyrazolo[1,5-a]pyrimidine-5-carboxylic esters by reacting with substituted β-diketo esters. · N-ethoxycarbonylthiourea derivative by reacting with ethoxycarbonyl isothiocyanate. · Heterobiaryl pyrazolo[3,4-b]pyridines by reacting with indole-3-carboxaldehyde.
Supplier:
MP Biomedicals
Description:
White solid, soluble in water or aqueous buffers (50 mg/ml); soluble in 0.01 N Sodium hydroxide (100 mg/mL - clear to slightly hazy, yellowish solution).
Catalog Number:
(77746-737)
Supplier:
AMBEED, INC
Description:
H-4-Pal-OH·2HCl ≥98%
Catalog Number:
(77405-096)
Supplier:
APOLLO SCIENTIFIC
Description:
3-(2-Pyridyl)-D-alanine
Catalog Number:
(101821-738)
Supplier:
Matrix Scientific
Description:
Matrix Scientific Part Number: 026167-500MG , MDL Number: MFCD07776933
Supplier:
BeanTown Chemical
Description:
CAS: 84199-98-4; EC No: 000-000-0; MDL No: MFCD01075660
Liquid; Molecular Formula: C9H11NO2; MW: 165.19
Boiling Point: 134°/12 mmHg
Refractive Index: 1.501
Catalog Number:
(10752-208)
Supplier:
Prosci
Description:
Voltage-gated proton (hydrogen) channels play an important role in cellular defense against acidic stress. NOX1 is a homolog of the catalytic subunit of the superoxide-generating NADPH oxidase of phagocytes, gp91phox. Three splice variants of NOX1 have been identified, NOH-1L, NOH-1S and NOH-1Lv. NOH-1S is a voltage-gated proton channel that participates in the regulation of cellular pH and is blocked by zinc. NOH-1L is a pyridine nucleotide-dependent oxidoreductase that generates superoxide and might conduct H(+) ions as part of its electron transport mechanism, whereas NOH-1S does not contain an electron transport chain. NOX1 have the potential to be effective treatments for a range of ischemic diseases.
Supplier:
APOLLO SCIENTIFIC
Description:
H-4-Pal-OH·2HCl 98%
Catalog Number:
(101821-700)
Supplier:
Matrix Scientific
Description:
Matrix Scientific Part Number: 026148-250MG , MDL Number: MFCD07367900
Supplier:
Matrix Scientific
Description:
Matrix Scientific Part Number: 016035-5G , MDL Number: MFCD02929397
Supplier:
AMBEED, INC
Description:
β-Dihydronicotinamide adenine dinucleotide disodium salt (NADH-Na₂, reduced form) 98%
Supplier:
MP Biomedicals
Description:
Soluble in water or aqueous buffers (50 mg/mL); soluble in 0.01 N Sodium hydroxide (100 mg/mL - clear to slightly hazy, yellowish solution).
Supplier:
BeanTown Chemical
Description:
CAS: 194673-12-6; EC No: 260-171-4; MDL No: MFCD00975005
Solid; Molecular Formula: C9H10F3NO3; MW: 237.18
Melting Point: 128-130°
Density (g/mL): 1.351
Supplier:
MP Biomedicals
Description:
Simple carbohydrate. Sucrose is hydrolyzed to glucose and fructose by dilute acids and by invertase, a yeast enzyme. Upon hydrolysis the optical rotation falls and is negative when the hydrolysis is complete. The mixture of glucose and fructose is known as "Invert sugar".
Supplier:
MP Biomedicals
Description:
Thymidine is a nucleoside composed of deoxyribose (a pentose sugar) joined to the pyrimidine base thymine.Deoxythymidine can be phosphorylated with one, two or three phosphoric acid groups, creating respectively dTMP, dTDP or dTTP (deoxythymidine mono- di- or triphosphate.It exists in solid form as small white crystals or white crystalline powder.The stability of deoxythymidine under standard temperature and pressure (STP) is very high.Thymidine is listed as a chemical teratogen.
Mainly used in forming hybrid cell lines wherein cells are incubated in HAT medium(hypoxanthine-aminopterin-thymidine medium) to give rise to monoclonal antibodies. Use in HT and HAT cocktails for hybridoma fusion, selection and cloning. Physical Appearance: White Powder Optical Rotation: (c=1, water) +17.5 - +19.5° UV/Visible Absorbance: λmax (0.1N HCl) 266 - 268 nm Solubility: Soluble in water, methanol, hot alcohol, hot acetone, hot ethyl acetate pyridine, glacial acetic acid and HCl (20 mg/mL-clear, colorless solution); sparingly soluble in hot chloroform
Catalog Number:
(76067-556)
Supplier:
Prosci
Description:
For WB starting dilution is: 1:1000
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