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| Product | Description | |
|---|---|---|
| N,N-Diisopropylethylamine | Diisopropylethylamine. CAS No. 7087-68-5. |  Pennsylvania PA |
| N,N-Diisopropylethylamine | N,N-Diisopropylethylamine. CAS No: 7087-68-5 |  Sarchem Laboratories New Jersey NJ |
| N,N-Diisopropylethylamine | N,N-Diisopropylethylamine. Group: Biochemicals. Alternative Names: 1,1'-Dimethyltriethylamine; Bis (1-methylethyl) ethylamine; DIEA; DIPEA; Diisopropylethylamine; Ethyl-N,N-diisopropylamine; Ethyldiisopropylamine; Huenig's base; Hunig's base; Hunig's reagent; N,N-Bis(1-methylethyl)-N-ethylamine; N,N-Diisopropylethylamine; N-Ethyl-N,N-diisopropylamine; N-Ethyl-N-(1-methylethyl)-2-propanamine; N-Ethyl-N-isopropylpropan-2-amine; N-Ethyl-N-propan-2-ylpropan-2-amine; N-Ethyldiisopropylamine; NSC 147491. Grades: Highly Purified. CAS No. 7087-68-5. Pack Sizes: 100g. Molecular Formula: C8H19N, Molecular Weight: 129.24. US Biological Life Sciences. |  Worldwide |
| N,N-Diisopropylethylamine | N,N-Diisopropylethylamine. We stock inventory in warehouses throughout the United States, allowing us to serve customers in all regions in a timely and cost effective manner. |  California |
| N,N'-Diisopropylethylamine 99+.7% (GC) | N,N'-Diisopropylethylamine 99+.7% (GC). Group: Biochemicals. Grades: GC. CAS No. 7087-68-5. Pack Sizes: 100ml, 250ml, 1L, 4L. US Biological Life Sciences. | Worldwide |
| N,N-diisopropylethylamine borane | N,N-diisopropylethylamine borane. Uses: Designed for use in research and industrial production. Additional or Alternative Names: Borane N,N-diisopropylethylamine complex, 88996-23-0, PubChem18302, Diisopropylethylamine borane, AGN-PC-00G71F, 253111_ALDRICH, boron;N-ethyl-N-propan-2-ylpropan-2-amine, FT-0642108. Product Category: Other. CAS No. 88996-23-0. Molecular formula: C8H22BN. Mole weight: 143.08. Purity: 0.96. IUPACName: boron;N-ethyl-N-propan-2-ylpropan-2-amine. Density: 0.822. Product ID: ACM88996230. Alfa Chemistry ISO 9001:2015 Certified. |  |
| N,N-Diisopropylethylamine (Hunigs base) | 100ml Pack Size. Group: Amines, Building Blocks. Formula: C8H19N. CAS No. 7087-68-5. Prepack ID 47362355-100ml. Molecular Weight 129.24. See USA prepack pricing. |  |
| N,N-Diisopropylethylamine p-toluenesulfonate salt | N,N-Diisopropylethylamine p-toluenesulfonate salt. Uses: Designed for use in research and industrial production. Additional or Alternative Names: 199818_ALDRICH, MolPort-003-927-406, EINECS 263-523-5, CID6454383, Ethyldiisopropylammonium p-toluenesulphonate, N-Ethyldiisopropylamine p-toluenesulfonate, N,N-Diisopropylethylamine p-toluenesulfonate salt, 62359-01-7. Product Category: Heterocyclic Organic CompoundAmine Salts. CAS No. 62359-01-7. Molecular formula: C8H19N.C7H8O3S. Mole weight: 301.44. Purity: 0.96. IUPACName: N-ethyl-N-propan-2-ylpropan-2-amine; 4-methylbenzenesulfonic acid. Canonical SMILES: CCN(C(C)C)C(C)C.CC1=CC=C(C=C1)S(=O)(=O)O. ECNumber: 263-523-5. Product ID: ACM62359017. Alfa Chemistry ISO 9001:2015 Certified. | |
| Fmoc-N-Me-Cys(Trt)-OH | Building block for introduction of N-α-methyl-cysteine amino-acid residues by Fmoc SPPS. Fmoc SPPS of Cysteine-Containing Peptides. Uses: Fmoc-n-me-cys(trt)-oh is a fmoc-protected derivative of n-methyl cysteine used as a building block to prepare peptide thioesters under acidic conditions. the residue attached to the amino group of n-methylcysteine can migrate to the cysteinyl thiol group, resulting in the formation of a peptide thioester. the introduction of this fmoc-protected derivative is best achieved using hatu as a coupling reagent in the presence of dipea (n, n-diisopropylethylamine). it can also be used to prepare fmoc-n-me-cys(trt)-oallyl intermediate for the solid-phase synthesis of dithiol triostin a. Additional or Alternative Names: N-α-Fmoc-N-α-methyl-S-trityl-L-cysteine. Product Category: Amino Acids. CAS No. 944797-51-7. Mole weight: 599.74. Product ID: ACM944797517. Alfa Chemistry ISO 9001:2015 Certified. | |
| HATU | HATU (1-[Bis(dimethylamino)methylene]-1H-1,2,3-triazolo[4,5-b]pyridinium 3-oxid hexafluorophosphate) is a reagent used in peptide coupling chemistry to generate an active ester from a carboxylic acid. HATU can be used along with Hünig's base (N,N-diisopropylethylamine, DIPEA) to form amide bonds [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 148893-10-1. Pack Sizes: 25 g; 50 g; 100 g. Product ID: HY-Y1703. |  |
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