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Albumin human

Supplier: ALADDIN SCIENTIFIC

Description: Product Introductionrecombinant, expressed in rice, suitable for cell culture, low endotoxin;It is a kind of recombinant human albumin (RHA) without animal origin. It is designed for cell culture applications and is a powerful medium supplement with superior performance to human albumin, bovine serum albumin and recombinant human albumin from other sources.It brings stable and consistent performance rather than variables related to hydrolysates and extracts. It is an ideal medium for Chinese hamster ovary (CHO), hybridoma, Vero, stem cell and primary cell culture medium.The recombinant variant is recommended for absorption, transport, metabolism and excretion (ADME) pharmacology; cell culture; drug delivery; and cell cryopreservation.

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2-Azido-1,3-dimethylimidazolinium hexafluorophosphate ≥98% (by HPLC)

Supplier: ALADDIN SCIENTIFIC

Description: Efficient diazo transfer reagent for the preparation of azides from primary amines. An alternative to tosyl azide with an easier-to-separate water soluble by-product。

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5-Acetylthiophene-2-carboxylic acid ≥97%

Supplier: ALADDIN SCIENTIFIC

Description: 5-Acetylthiophene-2-carboxylic acid ≥97%

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3-Aminobenzyl alcohol ≥98% (by GC)

Supplier: ALADDIN SCIENTIFIC

Description: Product Application:3-Aminobenzyl alcohol, is used as a reagent in the synthesis of quinone analogs as dynamin GTPase inhibitors. Also used as a reagent in the synthesis of pyrrolo[2,1-f][1,2,4]triazines as novel hedgehog signaling pathway inhibitors.

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2-(4-Aminophenyl)ethanol ≥98% (by GC)

Supplier: ALADDIN SCIENTIFIC

Description: 4-Aminophenethyl alcohol has been used: . as nonsymmetric monomer in the preparation of ordered [head-to-head (H-H) or tail-to-tail (T-T)] poly(amide-ester) . in the synthesis of 4-aminostyrene . in functionalization of graphene nanoplatelets

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2-Amino-3-formylchromone ≥98% (by HPLC, total nitrogen)

Supplier: ALADDIN SCIENTIFIC

Description: Product Description2-Amino-3-formylchromone (2-Amino-4-oxo-4H-1-benzopyran-3-carboxaldehyde) is a benzopyran derivative. It is a bicyclic heterocyclic molecule made up of a benzene ring fused to a heterocyclic pyran ring. It undergoes condensation with (R)-2-amino-2-phenylethanol to afford Schiff base ligand, which forms complexes with Cu(NO3)2 and Zn(NO3)2Product Application2-Amino-3-formylchromone may be used in the preparation of the following:• chiral Schiff base ligands (R)/(S)-2-amino-3-(((1-hydroxypropan-2-yl)imino)methyl)-4H-chromen-4-one• hydrazone derivatives, required for the synthesis of heterocyclic Schiff′s bases having antimicrobial activity[• N-{4-[(6-chloro-4-oxo-4H-chromen-3-ylmethylene)amino]phenyl}-3,5-dimethyl-benzofuran-2-carboxamide• N-{4-[(6-chloro-4-oxo-4H-chromen-3-ylmethylene)amino]phenyl}-1,4-dihydro-chromono [2,3-b]pyrrole-2-carboxamide• 6-chloro-3-{[4-(2-thioxo-3,6-dihydro-2H-1,3,4-thiadiazin-5-ylamino)phenylimino] methyl}- 4-oxo-4H -chromene• 3¬-(2-amino¬-4¬-oxo¬-4H¬-chromen¬-3-¬yl)methylidene)¬-6-¬ ethyl-¬2H-¬pyrano[3,2-¬c]quinolone-¬2,4,5(3H,6H)-trione

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5-Aminobenzimidazole ≥98% (by HPLC)

Supplier: ALADDIN SCIENTIFIC

Description: 5-Aminobenzimidazole ≥98% (by HPLC)

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2-Amino-6-iodopurine ≥98%

Supplier: ALADDIN SCIENTIFIC

Description: 2-Amino-6-iodopurine ≥98%

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4-Acetamidocyclohexanol (cis- and trans- mixture) ≥98% (by GC)

Supplier: ALADDIN SCIENTIFIC

Description: 4-Acetamidocyclohexanol (cis- and trans- mixture) ≥98% (by GC)

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2-Amino-N-[(1,1'-biphenyl)-4-yl]-N-(4-bromophenyl)-9,9-dimethylfluorene ≥98% (by HPLC)

Supplier: ALADDIN SCIENTIFIC

Description: 2-Amino-N-[(1,1'-biphenyl)-4-yl]-N-(4-bromophenyl)-9,9-dimethylfluorene ≥98% (by HPLC)

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3-(Allyloxy)oxetane ≥96%

Supplier: ALADDIN SCIENTIFIC

Description: 3-(Allyloxy)oxetane ≥96%

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(-)-ɑ-Phellandrene ≥65% (by GC)

Supplier: ALADDIN SCIENTIFIC

Description: Product Introduction:(R)-(-)-α-Phellandrene is a monoterpene derivative.Product Application:(R)-(-)-α-Phellandrene undergoes [4+2] cycloaddition with 2-naphthyl acetylenecarboxylate to form a chiral diene, which can act as a ligand for the rhodium-catalyzed asymmetric addition reactions. It may be used to synthesize (1S,5R)-5-(1-methylethyl)-2-methylidene-3-cyclohexen-1-yl hydroperoxide, which on reduction forms trans-yabunikkeol.

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