Pyrazine-2,6-diamine+hydrochloride
Supplier:
TCI America
Description:
CAS Number: 32499-64-2
MDL Number: MFCD00078171 Molecular Formula: C10H15NO3 Molecular Weight: 197.23 Purity/Analysis Method: >98.0% (GC) Form: Clear Liquid Boiling point (°C): 153 Specific Gravity (20/20): 1.15
Catalog Number:
(10067-468)
Supplier:
ALADDIN SCIENTIFIC
Description:
Shipped at 4°C. Store at -20°C. Store under desiccating conditions.
Supplier:
Invitrogen
Description:
Thermo Scientific Pierce EDC is a carboxyl- and amine-reactive zero-length crosslinker. EDC reacts with a carboxyl group first and forms an amine-reactive O-acylisourea intermediate that quickly reacts with an amino group to form an amide bond with release of an isourea by-product. The intermediate is unstable in aqueous solutions and so two-step conjugation procedures rely on N-hydroxysuccinimide (NHS) for stabilization. Failure to react with an amine will result in hydrolysis of the intermediate, regeneration of the carboxyl, and release of an N-substituted urea. A side reaction is the formation of an N-acylurea, which is usually restricted to carboxyls located in hydrophobic regions of proteins.
Catalog Number:
(10067-050)
Supplier:
Thermo Scientific Chemicals
Description:
A broad spectrum antibiotic
Catalog Number:
(IC15594925)
Supplier:
MP Biomedicals
Description:
A synthetic fluoroquinolone antibiotic used to treat urinary tract infections. It is effective against gram-positive and gram-negative bacteria, and its’ mode of action is to inhibit DNA gyrase and topoisomerase IV, thus
preventing cell division.
Supplier:
G-Biosciences
Description:
G-Biosciences’ cross-linking agents contain at least two reactive groups that are reactive towards numerous groups, including sulfhydryls, amines and carbohydrates, and create chemical covalent bonds between two or more molecules. Functional groups that can be targeted with cross-linking agents are primary amines, carboxyls, sulfhydryls, carbohydrates and carboxylic acids. Protein molecules have many of these functional groups and therefore proteins and peptides can be readily conjugated using cross-linking agents.
Supplier:
ALADDIN SCIENTIFIC
Description:
2-Amino-5-bromo-3-methylpyridine can be prepared from 2-amino-3-methylpyridine, via bromination.2-Amino-5-bromo-3-methylpyridine may be used to synthesize:5-bromo-2-chloro-3-methylpyridine;2-azidopyridine 1-oxide;2-amino-5-bromo-3-methylpyridine 1-oxide;2,5-dibromo-3-methyl pyridine;ethyl-3,6-dibromo-8-methylimidazo[1,2-a]pyridine-2-carboxylate.
Catalog Number:
(101822-626)
Supplier:
Matrix Scientific
Description:
Matrix Scientific Part Number: 026654-500MG , MDL Number: MFCD03933199
Catalog Number:
(101927-054)
Supplier:
Matrix Scientific
Description:
N-(3-Aminophenyl)methanesulfonamide
Supplier:
ALADDIN SCIENTIFIC
Description:
2-(4-Aminophenyl)-2-methylpropanenitrile ≥96%
Catalog Number:
(89149-064)
Supplier:
Enzo Life Sciences
Description:
Starting material for the synthesis of the antitumor drugs vinblastine and vincristine. It is less active as an inhibitor of tubulin self-assembly into microtubules than the latter two compounds.
Supplier:
ALADDIN SCIENTIFIC
Description:
2-(2-Aminophenyl)benzothiazole ≥97%
Supplier:
TCI America
Description:
CAS Number: 79794-75-5
MDL Number: MFCD00672869 Molecular Formula: C22H23ClN2O2 Molecular Weight: 382.89 Purity/Analysis Method: >98.0% (HPLC,T) Form: Crystal Melting point (°C): 137
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