A directory of where to buy chemicals in the USA, including: distributors, industrial manufacturers, bulk supplies and wholesalers of raw ingredients & finished goods.
Fmoc-O-trityl-D-serine. Group: Biochemicals. Alternative Names: Fmoc-D-Ser(Trt)-OH. Grades: Highly Purified. CAS No. 212688-51-2. Pack Sizes: 2g, 5g, 10g, 25g. US Biological Life Sciences.
Worldwide
Fmoc-O-trityl-D-serine 98+% (HPLC)
Fmoc-O-trityl-D-serine 98+% (HPLC). Group: Biochemicals. Grades: Reagent Grade. Pack Sizes: 1g, 5g, 25g. US Biological Life Sciences.
Worldwide
Fmoc-O-trityl-D-threonine
Side-chain can be selectively deprotected on the solid phase with 1% TFA/5% triisopropylsilane. Synonyms: Fmoc-D-Thr(Trt)-OH; Fmoc-D-Thr(OTrt)-OH. Grades: ≥ 98% (HPLC). CAS No. 682800-84-6. Molecular formula: C38H33NO5. Mole weight: 583.70.
Fmoc-O-trityl-D-threonine
Fmoc-O-trityl-D-threonine. Uses: Designed for use in research and industrial production. Additional or Alternative Names: FMOC-D-THR(TRT)-OH. Appearance: Off-white to brown crystals. CAS No. 682800-84-6. Molecular formula: C38H33NO5. Mole weight: 583.7. Purity: 98%+. IUPACName: (2R,3S)-2-(9H-fluoren-9-ylmethoxycarbonylamino)-3-trityloxybutanoicacid. Canonical SMILES: CC(C(C(=O)O)NC(=O)OCC1C2=CC=CC=C2C3=CC=CC=C13)OC(C4=CC=CC=C4)(C5=CC=CC=C5)C6=CC=CC=C6. Product ID: ACM682800846. Alfa Chemistry ISO 9001:2015 Certified.
Fmoc-O-trityl-D-threonine
Fmoc-O-trityl-D-threonine. Group: Biochemicals. Alternative Names: Fmoc-D-Thr(Trt)-OH. Grades: Highly Purified. CAS No. 682800-84-6. Pack Sizes: 2g, 5g, 10g, 25g. US Biological Life Sciences.
Worldwide
Fmoc-O-trityl-D-threonine 98+% (HPLC)
Fmoc-O-trityl-D-threonine 98+% (HPLC). Group: Biochemicals. Grades: Reagent Grade. Pack Sizes: 1g, 5g, 25g. US Biological Life Sciences.
Fmoc-O-trityl-L-threonine. Group: Biochemicals. Alternative Names: Fmoc-L-Thr(Trt)-OH. Grades: Highly Purified. CAS No. 133180-01-5. Pack Sizes: 2g, 5g, 10g, 25g, 50g. US Biological Life Sciences.
Worldwide
Fmoc-O-trityl-L-threonine 98+% (HPLC)
Fmoc-O-trityl-L-threonine 98+% (HPLC). Group: Biochemicals. Grades: Reagent Grade. Pack Sizes: 1g, 5g, 25g, 100g. US Biological Life Sciences.
Worldwide
Fmoc-PABA-OH
Standard building block for introduction of p-aminobenzoic acid residues by Fmoc SPPS. Uses: Peptide synthesis. Additional or Alternative Names: Fmoc-PABA-OH, N-α-Fmoc-p-aminobenzoic acid,Fmoc-4-Abz-OH. Product Category: Amino Acids. CAS No. 185116-43-2. Mole weight: 359.37. Product ID: ACM185116432. Alfa Chemistry ISO 9001:2015 Certified. Categories: 4-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)benzoic acid.
Fmoc-PAL
Fmoc-PAL. Group: Biochemicals. Alternative Names: 5-[4-[[[ (9H-Fluoren-9-ylmethoxy) carbonyl]amino]methyl]-3, 5-dimethoxyphenoxy]-pentanoic acid. Grades: Highly Purified. CAS No. 115109-65-4. Pack Sizes: 250mg, 500mg, 1g, 2g, 5g. Molecular Formula: C29H31NO7. US Biological Life Sciences.
Worldwide
Fmoc-Pal-Linker
It is a reagent for the mild solid-phase synthesis of C-terminal peptide amides. Synonyms: Pal Linker; Fmoc-Pal-Linker; 5- (4- (9-Fluorenylmethyloxycarbonyl) Aminomethyl-3, 5-Dimethoxyphenoxy) Valeric Acid; 5-[3,5-Dimethoxy-4-(Fmoc-Aminomethyl)Phenoxy]Pentanoic Acid; 5-(4-(((((9H-Fluoren-9-Yl)Methoxy)Carbonyl)Amino)Methyl)-3,5-Dimethoxyphenoxy)Pentanoic Acid. Grades: ≥ 95% (HPLC). CAS No. 115109-65-4. Molecular formula: C29H31NO7. Mole weight: 505.5.
Fmoc-Pal Linker ≥95% (HPLC)
Fmoc-Pal Linker ≥95% (HPLC). Group: Biochemicals. Grades: Reagent Grade. CAS No. 115109-65-4. Pack Sizes: 1g, 5g. US Biological Life Sciences.
Worldwide
Fmoc-p-amino-benzoic acid
Fmoc-p-amino-benzoic acid. Group: Biochemicals. Grades: Highly Purified. CAS No. 15026-42-1. Pack Sizes: 25g, 50g, 100g, 250g, 500g. US Biological Life Sciences.
Worldwide
Fmoc-PEG2-Suc-OH
N-(Fmoc-8-amino-3,6-dioxa-octyl)succinamic acid is a synthetic molecule that belongs to the group of succinamic acids. Succinamic acids are organic molecules that have two carboxylic acid groups and an amide group linked to a cyclic structure. N-(Fmoc-8-amino-3,6-dioxa-octyl)succinamic acid is a modified succinamic acid that has an Fmoc (9-fluorenylmethyloxycarbonyl) protecting group attached to the amino group. The Fmoc group protects the amino group during synthesis, and it can be removed under mild conditions to expose the amino group for further functionalization. This property makes N-(Fmoc-8-amino-3,6-dioxa-octyl)succinamic acid a valuable building block for the synthesis of other molecules, such as peptides and proteins. Uses: N-(fmoc-8-amino-3,6-dioxa-octyl)succinamic acid has various applications in scientific experiments, particularly in the synthesis of peptides and proteins. the molecule can be used as a building block for the preparation of various peptides and proteins, such as fmoc-protected peptides, hydrogels, and bioconjugates. Additional or Alternative Names: N-(Fmoc-8-amino-3,6-dioxa-octyl)succinamic acid, 1-(9H-Fluoren-9-yl)-3,14-dioxo-2,7,10-trioxa-4,13-diazaheptadecan-17-oic acid, Fmoc-PEG-SU. Product Category: Amino Acids. CAS No. 613245-91-3. Molecular formula: C25H30N2O7. Mole weight: 470.5. Purity: Peak Area by HPLC ≥95%. IUPACName: 4-[2-[2-[2-(9H-fluoren-9-ylmethoxycarbonylamino)ethoxy]etho
FMOC-PEG5K-Succinimide Butanoate
average Mn 5000. Group: Poly(ethylene glycol) and poly(ethylene oxide).
FMOC-PEG5K-Succinimide Butanoate
Polyethylene glycol (PEG) compounds contain a polyether unit, commonly expressed as R1-(O-CH2-CH2)n-O-R2. They are generally biocompatible, non-toxic and stable in both organic and aqueous solutions, and so are extensively used in biological applications, as well as nanotechnology and materials research. Proteins with PEG chain modifications and compounds encapsulated in PEG liposomes exhibit a longer half-life in vivo than their non-PEGylated counterparts, a phenomenon known as PEG shielding. Functionalised PEG lipids and phospholipids can be used for protein-PEG conjugation. Uses: Activated peg derivatives can be used to modify peptides, proteins, or in other bioconjugation applications. pegylated materials have found broad use in drug delivery systems, virology, and immunology, as the incorporation of peg improves pharmacological properties such as increased water solubility, enhanced resistance to degradation (protein hydrolysis), increased circulation half-life, and reduced antigenicity. in addition to pegylation, activated peg derivatives can also be used to form networks for tissue engineering or drug delivery applications, depending on the architecture and reactivity. Group: Poly(ethylene glycol) and poly(ethylene oxide). Molecular formula: average Mn 5000.
Fmoc-pentafluoro-D-b-homophenylalanine
Fmoc-pentafluoro-D-b-homophenylalanine. Group: Biochemicals. Alternative Names: Fmoc-D-b-HomoPhe(F)5-OH; Fmoc- (R) -3-amino-4- (pentafluorophenyl) butyric acid. Grades: Highly Purified. CAS No. 269398-94-9. Pack Sizes: 25mg, 50mg, 100mg, 250mg. US Biological Life Sciences.
Worldwide
Fmoc-pentafluoro-D-b-homophenylalanine 98+%
Fmoc-pentafluoro-D-b-homophenylalanine 98+%. Group: Biochemicals. Grades: Reagent Grade. Pack Sizes: 100mg, 250mg. US Biological Life Sciences.