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| Product | Description | |
|---|---|---|
| 2-Aminoisobutyric acid | 2-Aminoisobutyric acid. Group: Biochemicals. Alternative Names: a-Amino isobutyric acid. Grades: Highly Purified. CAS No. 62-57-7. Pack Sizes: 250g, 500g, 1kg, 2kg, 5kg. Molecular Formula: C4H9NO2. US Biological Life Sciences. |  Worldwide |
| 2-Aminoisobutyric acid | 2-Aminoisobutyric acid. Uses: Designed for use in research and industrial production. Additional or Alternative Names: Alpha-aminoisobutanoicacid. Product Category: Heterocyclic Organic Compound. Appearance: White crystalline powder. CAS No. 62-57-7. Molecular formula: C4H9NO2. Mole weight: 103.12. Purity: 0.98. IUPACName: 2-Amino-2-methylpropanoic acid. Canonical SMILES: CC(C)(C(=O)O)N. Density: 1.1602 g/cm³. Product ID: ACM62577. Alfa Chemistry ISO 9001:2015 Certified. |  |
| 2-Aminoisobutyric Acid | 2-Aminoisobutyric acid is a natural product found in Garcinia mangostana, Apis cerana, and Caenorhabditis elegans. Synonyms: α-Aminoisobutyric acid; 2-Methylalanine; H-Aib-OH; α,α-Dimethylglycine. Grade: 98%. CAS No. 62-57-7. Molecular formula: C4H9NO2. Mole weight: 103.12. |  |
| 2-Aminoisobutyric acid-[15N] | 2-Aminoisobutyric acid-[15N] is a labelled 2-Aminoisobutyric acid. 2-Aminoisobutyric acid is a non-proteinogenic amino acid that is rare in nature. Synonyms: 2-Aminoisobutyric-15N acid. Grade: 98% by HPLC; 98% atom 15N. Molecular formula: C4H9[15N]O2. Mole weight: 104.11. | |
| 2-Aminoisobutyric acid benzyl ester | 2-Aminoisobutyric acid benzyl ester. Synonyms: H-Aib-OBzl; H-(Me)Ala-OBzl; 2-Methylalanine benzyl ester. CAS No. 55456-40-1. Molecular formula: C11H15NO2. Mole weight: 193.25. | |
| 2-Aminoisobutyric acid benzyl ester hydrochloride | 2-Aminoisobutyric acid benzyl ester hydrochloride (CAS# 60421-20-7) is a useful research chemical compound. Synonyms: H-Aib-OBzl HCl; H-(Me)Ala-OBzl HCl; 2-Methylalanine benzyl ester hydrochloride. Grade: ≥ 98 % (HPLC). CAS No. 60421-20-7. Molecular formula: C11H16ClNO2. Mole weight: 229.71. | |
| 2-Aminoisobutyric acid ethyl ester hydrochloride | 2-Aminoisobutyric acid ethyl ester hydrochloride. Uses: An amino acid derivative used in pharmaceutical compositions. Synonyms: H-Aib-OEt HCl; H-(Me)Ala-OEt HCl; 2-Methylalanine ethyl ester hydrochloride. Grade: ≥ 99% (HPLC). CAS No. 17288-15-2. Molecular formula: C6H14ClNO2. Mole weight: 167.64. | |
| 2-Aminoisobutyric acid ethyl ester hydrochloride 99+% (HPLC) | 2-Aminoisobutyric acid ethyl ester hydrochloride 99+% (HPLC). Group: Biochemicals. Grades: Reagent Grade. Pack Sizes: 1g, 5g, 25g. US Biological Life Sciences. | Worldwide |
| 2-Aminoisobutyric acid methyl ester hydrochloride | 2-Aminoisobutyric acid methyl ester hydrochloride. Synonyms: H-Aib-OMe HCl; H-(Me)Ala-OMe HCl; 2-Methylalanine methyl ester hydrochloride. Grade: ≥ 99% (HPLC). CAS No. 15028-41-8. Molecular formula: C5H12ClNO2. Mole weight: 153.61. | |
| 2-Aminoisobutyric acid t-butyl ester | 2-Aminoisobutyric acid t-butyl ester. Group: Biochemicals. Grades: Highly Purified. CAS No. 4512-32-7. Pack Sizes: 100mg, 250mg. Molecular Formula: C8H17NO2, Molecular Weight: 159.229999999999. US Biological Life Sciences. | Worldwide |
| 2-Aminoisobutyric acid t-butyl ester hydrochloride | 2-Aminoisobutyric acid t-butyl ester hydrochloride. Synonyms: H-Aib-OtBu HCl; H-(Me)Ala-OtBu HCl; 2-Methylalanine t-butyl ester hydrochloride. CAS No. 84758-81-6. Molecular formula: C8H18ClNO2. Mole weight: 195.69. | |
| 3-Aminoisobutyric acid | 3-Aminoisobutyric acid (β-Aminoisobutyric acid) has anti-inflammatory and antioxidant effects. 3-Aminoisobutyric acid increases the expression of brown adipocyte-specific genes in white adipose tissue and fatty acid β-oxidation in hepatocytes. 3-Aminoisobutyric acid attenuates insulin resistance and inflammation induced by palmitate or a high fat diet via an AMPK - PPARδ-dependent pathway in mice. 3-Aminoisobutyric acid is a catabolic metabolite of thymine and valine in skeletal muscle [1] [2] [3] [4]. Uses: Scientific research. Group: Natural products. Alternative Names: β-Aminoisobutyric acid; BAIBA. CAS No. 144-90-1. Pack Sizes: 10 mM * 1 mL; 100 mg. Product ID: HY-W012974. |  |
| 3-Aminoisobutyric acid (Standard) | 3-Aminoisobutyric acid (Standard) is the analytical standard of 3-Aminoisobutyric acid. This product is used for research and analytical applications. 3-Aminoisobutyric acid (β-Aminoisobutyric acid) exhibits anti-inflammatory and antioxidant effects. It increases the expression of brown fat cell-specific genes in white adipose tissue and enhances fatty acid β-oxidation in hepatocytes. 3-Aminoisobutyric acid alleviates insulin resistance and inflammation induced by palmitic acid or a high-fat diet in mice via the AMPK - PPARδ -dependent pathway. 3-Aminoisobutyric acid is a catabolite of thymine and valine in skeletal muscle [1] [2] [3] [4]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: β-Aminoisobutyric acid (Standard); BAIBA (Standard). CAS No. 144-90-1. Pack Sizes: 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-W012974R. | |
| a-Aminoisobutyric acid 99+% | a-Aminoisobutyric acid 99+%. Group: Biochemicals. Grades: Reagent Grade. Pack Sizes: 25g, 100g, 250g, 1Kg. US Biological Life Sciences. | Worldwide |
| a-Aminoisobutyric acid methyl ester hydrochloride 99+% (HPLC) | a-Aminoisobutyric acid methyl ester hydrochloride 99+% (HPLC). Group: Biochemicals. Grades: Reagent Grade. Pack Sizes: 1g, 5g, 25g, 100g, 250g. US Biological Life Sciences. | Worldwide |
| a-Aminoisobutyric acid tert-butyl ester hydrochloride 98+% (HPLC) | a-Aminoisobutyric acid tert-butyl ester hydrochloride 98+% (HPLC). Group: Biochemicals. Grades: Reagent Grade. Pack Sizes: 1g, 5g, 25g. US Biological Life Sciences. | Worldwide |
| -alpha-Aminoisobutyric acid Methyl ester hydrochloride | -alpha-Aminoisobutyric acid methyl ester hydrochloride. Group: Biochemicals. Alternative Names: Aib-OMe·HCl; a-Methylalanine methyl ester hydrochloride. Grades: Highly Purified. CAS No. 15028-41-8. Pack Sizes: 2g, 5g, 10g, 25g, 50g. US Biological Life Sciences. | Worldwide |
| Boc-a-aminoisobutyric acid | Boc-a-aminoisobutyric acid. Group: Biochemicals. Alternative Names: Boc-Aib-OH; Boc-a-methylalanine. Grades: Highly Purified. CAS No. 30992-29-1. Pack Sizes: 25g, 50g, 100g. US Biological Life Sciences. | Worldwide |
| Boc-a-aminoisobutyric acid | Boc-a-aminoisobutyric acid. Synonyms: Boc-Aib-OH; Boc-a-methylalanine; Boc Aib OH. Grade: ≥ 98% (HPLC). CAS No. 30992-29-1. Molecular formula: C9H17NO4. Mole weight: 203.24. | |
| Boc-a-aminoisobutyric acid 98+% (HPLC) | Boc-a-aminoisobutyric acid 98+% (HPLC). Group: Biochemicals. Grades: Reagent Grade. Pack Sizes: 5g, 25g, 100g. US Biological Life Sciences. | Worldwide |
| Boc-a-aminoisobutyric acid N-hydroxysuccinimide ester 98+% (HPLC) | Boc-a-aminoisobutyric acid N-hydroxysuccinimide ester 98+% (HPLC). Group: Biochemicals. Grades: Reagent Grade. Pack Sizes: 1g, 5g. US Biological Life Sciences. | Worldwide |
| Boc-α-aminoisobutyric acid N-hydroxysuccinimide ester | Boc-α-aminoisobutyric acid N-hydroxysuccinimide ester. Synonyms: Boc-Aib-OSu; Boc-α-methyl-L-alanine N-hydroxysuccinimide ester; Boc Aib OSu. Grade: ≥ 98% (HPLC). CAS No. 104055-39-2. Molecular formula: C13H20N2O6. Mole weight: 300.31. | |
| Boc-alpha-aminoisobutyric acid N-hydroxysuccinimide ester | Boc-alpha-aminoisobutyric acid N-hydroxysuccinimide ester. Group: Biochemicals. Alternative Names: Boc-Aib-OSu; Boc-a-methyl-L-alanine N-hydroxysuccinimide ester. Grades: Highly Purified. CAS No. 104055-39-2. Pack Sizes: 2g, 5g. US Biological Life Sciences. | Worldwide |
| Boc-N-methyl-aminoisobutyric acid | Boc-N-methyl-aminoisobutyric acid. Group: Biochemicals. Grades: Highly Purified. CAS No. 146000-39-7. Pack Sizes: 250mg, 500mg, 1g, 2g, 5g. Molecular Formula: C10H19NO4. US Biological Life Sciences. | Worldwide |
| DL-3-Aminoisobutyric Acid | DL-3-Aminoisobutyric Acid. Synonyms: Propanoic acid, 3-amino-2-methyl-; DL-β-Aminoisobutyric acid; β-Aminoisobutyric acid; 3-Aminoisobutanoate; 2-Methyl-3-aminopropanoic acid; DL-3-Amino-2-methylpropionic acid; 2-(Aminomethyl)propionic acid; alpha-Methyl-beta-alanine; 2-Methyl-beta-alanine; (±)-β-Aminoisobutyric acid. Grade: ≥95%. CAS No. 144-90-1. Molecular formula: C4H9NO2. Mole weight: 103.12. | |
| DL-3-Aminoisobutyric acid (BAIBA) | 3-Aminoisobutyric acid (or β-aminoisobutyric acid, BAIBA) is a product formed by the catabolism of thymine. During exercise, the increase of PGC-1α protein triggers the secretion of BAIBA from exercising muscles to blood (concentration 2 to 3uM in human serum). When BAIBA reaches the white fat tissue, it activates the expression of thermogenic genes via PPARα receptors, resulting in a browning of white fat cells. One of the consequences of the BAIBA activity is the increase of the background metabolism of the BAIBA target cells. It has recently been postulated to play a role in cell metabolism, how body burns fat and regulates insulin, triglycerides, and total cholesterol. Group: Biochemicals. Alternative Names: BAIBA; 3-amino-2-methylpropanoic acid; 2-(aminomethyl)propionic acid; 2-Methyl-beta-alanine3-Amino-2-methylpropanoate; 3-Aminoisobutanoate; 3-Aminoisobutanoic acid; 3-aminoisobutyric acid; alpha-Methyl-beta-alanine; β-aminoisobutyric acid; DL-beta-aminoisobutyric acid. Grades: Highly Purified. CAS No. 144-90-1. Pack Sizes: 1g, 5g, 10g, 25g. Molecular Formula: C?H?NO?, Molecular Weight: 103.12. US Biological Life Sciences. | Worldwide |
| DL-3-Aminoisobutyric acid hydrate | DL-3-Aminoisobutyric acid hydrate. Synonyms: H-DL-Aib(3)-OH H2O; H-DL-β-Aib-OH H2O; DL-3-Amino-2-methylpropanoic acid hydrate. Grade: 95%. CAS No. 214139-20-5. Molecular formula: C4H11NO3. Mole weight: 121.14. | |
| DL-beta-Aminoisobutyric Acid | DL-beta-Aminoisobutyric Acid. Synonyms: alpha-Methyl-Beta-alanine; 3-amino-2-methylpropionic acid; DL-3-Aminoisobutyric acid; H-ALA(ME)-OH; H-AIB-OH; 3-amino-2(R,S)-methylpropionic acid; DL-3-Amino-2-methyl-propionic acid; α-Methyl-β-alanine. Grade: ? 95%. CAS No. 10569-72-9. Molecular formula: C4H9NO2. Mole weight: 103.12. | |
| Fmoc-a-aminoisobutyric acid 99+% (HPLC) | Fmoc-a-aminoisobutyric acid 99+% (HPLC). Group: Biochemicals. Grades: Reagent Grade. Pack Sizes: 1g, 5g, 25g, 100g. US Biological Life Sciences. | Worldwide |
| Fmoc-α-aminoisobutyric acid | Fmoc-α-aminoisobutyric acid. Synonyms: Fmoc-Aib-OH; Fmoc-α-methylalanine. Grade: ≥ 99% (HPLC). CAS No. 94744-50-0. Molecular formula: C19H19NO4. Mole weight: 325.36. | |
| N-(((9H-Fluoren-9-yl)methoxy)carbonyl)-2-aminoisobutyric acid tritylcarboxamidomethyl polyethyleneglycol resin | N-(((9H-Fluoren-9-yl)methoxy)carbonyl)-2-aminoisobutyric acid tritylcarboxamidomethyl polyethyleneglycol resin. Synonyms: Fmoc-Aib-TrtA-PEG Resin; Fmoc-(Me)Ala-TrtA-PEG Resin; N-(((9H-Fluoren-9-yl)methoxy)carbonyl)-2-methylalanine tritylcarboxamidomethyl polyethyleneglycol resin. | |
| N-(((9H-Fluoren-9-yl)methoxy)carbonyl)-DL-3-aminoisobutyric acid | N-(((9H-Fluoren-9-yl)methoxy)carbonyl)-DL-3-aminoisobutyric acid. Synonyms: Fmoc-DL-Aib(3)-OH; Fmoc-DL-β-Aib-OH; N-(((9H-Fluoren-9-yl)methoxy)carbonyl)-DL-3-amino-2-methylpropanoic acid. Grade: ≥ 95%. CAS No. 186320-19-4. Molecular formula: C19H19NO4. Mole weight: 325.37. | |
| N-((Benzyloxy)carbonyl)-DL-3-aminoisobutyric acid | N-((Benzyloxy)carbonyl)-DL-3-aminoisobutyric acid. Synonyms: Z-DL-Aib(3)-OH; Z-DL-β-Aib-OH; N-((Benzyloxy)carbonyl)-DL-3-amino-2-methylpropanoic acid. Grade: 95%. CAS No. 101642-77-7. Molecular formula: C12H15NO4. Mole weight: 237.26. | |
| N-Methyl-a-aminoisobutyric acid hydrochloride 98+% (TLC) | N-Methyl-a-aminoisobutyric acid hydrochloride 98+% (TLC). Group: Biochemicals. Grades: Reagent Grade. Pack Sizes: 250mg, 1g, 5g. US Biological Life Sciences. | Worldwide |
| N-Methyl-α-aminoisobutyric acid hydrochloride | N-Methyl-α-aminoisobutyric acid hydrochloride. Synonyms: N-Me-Aib-OH HCl; N-Methyl-α-methylalanine hydrochloride. Grade: ≥ 98% (TLC). CAS No. 2566-34-9. Molecular formula: C5H11NO2·HCl. Mole weight: 153.62. | |
| N-Methyl-alpha-aminoisobutyric acid hydrochloride | N-Methyl-alpha-aminoisobutyric acid hydrochloride. Group: Biochemicals. Alternative Names: N-Me-Aib-OH·HCl; N-Methyl-a-methylalanine hydrochloride. Grades: Highly Purified. CAS No. 2566-34-9. Pack Sizes: 500mg, 1g, 2g, 5g. US Biological Life Sciences. | Worldwide |
| N-Methyl-aMinoisobutyric acid Methyl ester hydrochloride | N-Methyl-aMinoisobutyric acid Methyl ester hydrochloride. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 500mg, 1g, 2g, 5g. US Biological Life Sciences. | Worldwide |
| N-((tert-Butoxy)carbonyl)-DL-3-aminoisobutyric acid | N-((tert-Butoxy)carbonyl)-DL-3-aminoisobutyric acid. Synonyms: Boc-DL-Aib(3)-OH; Boc-DL-β-Aib-OH; N-((tert-Butoxy)carbonyl)-DL-3-amino-2-methylpropanoic acid; 2-methyl-3-(tert-butyloxycarbonylamino)propionic acid; 3-(Tert-butoxycarbonylamino)-2-methylpropionic acid; N-tert-butoxycarbonyl-3-amino-2(RS)-methylpropionic acid; Boc-DL-3-Aminoisobutyric acid. Grade: ≥ 95%. CAS No. 16948-10-0. Molecular formula: C9H17NO4. Mole weight: 203.24. | |
| rac-3-aminoisobutyric acid hydrochloride | rac-3-aminoisobutyric acid hydrochloride. Group: Biochemicals. Alternative Names: 3-Amino-2-methylpropanoic acid hydrate; 3-Amino-2-methylpropanoic acid hydrochloride; 2-Methyl-b-alanine hydrochloride. Grades: Highly Purified. CAS No. 28267-25-6. Pack Sizes: 1g, 2g, 5g, 10g, 25g. Molecular Formula: C4H10ClNO2. US Biological Life Sciences. | Worldwide |
| Z-a-aminoisobutyric acid 99+% | Z-a-aminoisobutyric acid 99+%. Group: Biochemicals. Grades: Reagent Grade. Pack Sizes: 5g, 25g, 100g. US Biological Life Sciences. | Worldwide |
| Z-α-aminoisobutyric acid | Z-α-aminoisobutyric acid. Synonyms: Z-Aib-OH; Z-α-methylalanine. Grade: ≥ 99% (HPLC). CAS No. 15030-72-5. Molecular formula: C12H15NO4. Mole weight: 237.30. | |
| Z-alpha-aminoisobutyric acid | Z-alpha-aminoisobutyric acid. Group: Biochemicals. Alternative Names: Z-Aib-OH; Z-a-methylalanine. Grades: Highly Purified. CAS No. 15030-72-5. Pack Sizes: 2g, 5g, 10g, 25g, 50g. US Biological Life Sciences. | Worldwide |
| Z-N-methyl-a-aminoisobutyric acid 99+% (HPLC) | Z-N-methyl-a-aminoisobutyric acid 99+% (HPLC). Group: Biochemicals. Grades: Reagent Grade. Pack Sizes: 1g, 5g, 25g. US Biological Life Sciences. | Worldwide |
| Z-N-methyl-α-aminoisobutyric acid | Z-N-methyl-α-aminoisobutyric acid. Synonyms: Z-N-Me-Aib-OH; Z-N-methyl-α-methylalanine. Grade: ≥ 99% (HPLC). CAS No. 144332-60-5. Molecular formula: C13H17NO4. Mole weight: 251.28. | |
| Z-N-methyl-alpha-aminoisobutyric acid | Z-N-methyl-alpha-aminoisobutyric acid. Group: Biochemicals. Alternative Names: Z-N-Me-Aib-OH; Z-N-methyl-a-methylalanine. Grades: Highly Purified. CAS No. 144332-60-5. Pack Sizes: 2g, 5g, 10g, 25g. US Biological Life Sciences. | Worldwide |
| 2-[[[ (1, 1-Dimethylethoxy) carbonyl]amino]methyl]-propanoic-3, 3, 3-d3 Acid Phenylmethyl Ester | 2-[[[ (1, 1-Dimethylethoxy) carbonyl]amino]methyl]-propanoic-3, 3, 3-d3 Acid Phenylmethyl Ester is an intermediate in the synthesis of labelled 3-Aminoisobutyric Acid (A611587). Unlabelled 3-Aminoisobutyric Acid (A611585) is a substituted β-alanines and is used for preparation and isolation of D(-)- β-Aminoisobutyric Acid. Group: Biochemicals. Grades: Highly Purified. CAS No. 375379-70-7. Pack Sizes: 25mg, 50mg. Molecular Formula: C16H20D3NO4. US Biological Life Sciences. | Worldwide |
| 2-Methylalanine | 2-Methylalanine. Group: Biochemicals. Alternative Names: 2,2-Dimethylglycine; 2-Amino-2-methylpropanoic Acid; 2-Amino-2-methylpropionic Acid; 2-Aminoisobutyric Acid; 2-Methylalanine; 21: PN: WO2005055994 PAGE: 50 claimed sequence; AIB; Aminoisobutyric Acid; NSC 16590; α,α-Dimethylglycine; α-Aminoisobutanoic Acid; α-Aminoisobutyric Acid; α-Methylalanine. Grades: Highly Purified. CAS No. 62-57-7. Pack Sizes: 25g. US Biological Life Sciences. | Worldwide |
| (+/-)-3-Amino-iso-butyric Acid-[2,3,3-d3] | (+/-)-3-Amino-iso-butyric Acid-[2,3,3-d3]. Synonyms: beta-Aminoisobutyric acid-d3. Grade: 98% atom D. CAS No. 1219803-65-2. Molecular formula: C4H6D3NO2. Mole weight: 106.14. | |
| 3-[(tert-Butoxycarbonyl)amino]-2-methylpropanoic-d3 Acid | 3-[(tert-Butoxycarbonyl)amino]-2-methylpropanoic-d3 Acid is labelled (R) -3- ( (tertButoxycarbonyl) amino) -2-methylpropanoic Acid (B692230), which has been used as a reactant in the preparation of cryptophycin B and arenastatin A, potent antiumor macrolides. 3-[(tert-Butoxycarbonyl)amino]-2-methylpropanoic-d3 Acid is an intermediate in the synthesis of labelled 3-Aminoisobutyric Acid (A611587). Unlabelled 3-Aminoisobutyric Acid (A611585) is a substituted β-alanines and is used for preparation and isolation of D(-)- β-Aminoisobutyric Acid. Group: Biochemicals. Grades: Highly Purified. CAS No. 375379-71-8. Pack Sizes: 10mg, 25mg. Molecular Formula: C9H14D3NO4. US Biological Life Sciences. | Worldwide |
| Alamethicin (Antibiotic U-22324) | Alamethicin is a peptide antibiotic, produced by the fungus Trichoderma viride. Alamethicin contains the non-proteinogenic amino acid 2-aminoisobutyric acid (Aib), which strongly induces helical peptide structures. In cell membranes, it forms voltage-dependent ion channels by aggregation of four to six molecules. Group: Biochemicals. Alternative Names: (3S,12R)-1-((S)-1-((6S,12S,15S,21S,30S)-1-((R)-1-(2-Acetamido-2- methylpropanoyl) pyrrolidin-2-yl) -15- (3-amino-3-oxopropyl) -30-isobutyl-21-isopropyl- 3, 3, 6, 9, 9, 2, 18, 18, 24, 24, 33, 33-dodecamethyl-1, 4, 7, 10, 13, 16, 19, 22, 25, 28, 31- undecaoxo-2, 5, 8, 11, 14, 17, 20, 23, 26, 29, 32-undecaazatetratri acontan-34- oyl)pyrrolidin-2-yl)-12-(((R)-5-amino-1-(((S)-1-hydroxy-3-phenylpropan-2-yl)amino)-1, 5-dioxopentan-2-yl)carbamoyl)-3-isopropyl-6,6,9,9-tetramethyl-1,4,7,10-tetraoxo-2,5, 8,11-tetraazapentadecan-15-oic Acid; Antibiotic U-22324. Grades: Purified. CAS No. 27061-78-5. Pack Sizes: 1mg, 5mg, 10mg. Molecular Formula: C??H???N??O??, Molecular Weight: 1964.31. US Biological Life Sciences. | Worldwide |
| Boc-Aib-OH | Standard building block for introduction of aminoisobutyric acid amino-acid residues by Boc SPPS. Uses: Peptide synthesis. Additional or Alternative Names: Boc-Aib-OH, N-α-t.-Boc-α-aminoisobutyric acid, N-α-t.-Boc-α-methylalanine. Product Category: Amino Acids. CAS No. 30992-29-1. Mole weight: 203.24. Product ID: ACM30992291. Alfa Chemistry ISO 9001:2015 Certified. | |
| Boc-α-Methylalanine | Boc-α-Methylalanine. Group: Biochemicals. Alternative Names: N-[ (1, 1-Dimethylethoxy) carbonyl]-2-methylalanine; N-Carboxy-2-methylalanine, N-tert-Butyl Ester; 2-(((tert-Butoxy)carbonyl)amino)-2-methylpropanoic Acid; 2-(Boc-amino)isobutyric Acid; 2- (tert-Butoxycarbonylamino) isobutanoic Acid; 2- (tert-Butoxycarbonylamino) isobutyric Acid; 2-(tert-Butoxycarboxylamino)-2-methylpropanoic Acid; 2- (tert-Butyloxycarbonylamino) isobutanoic Acid; 2-Methyl-2- ( (t-butyloxycarbonyl) amino) propionic Acid; 2-[(tert-Butoxycarbonyl)amino]-2-methylpropionic Acid; 208: PN: WO2004005478 PAGE: 71 claimed protein; Boc-2-methylalanine; N-(tert-Butoxycarbonyl)-2,2-dimethylglycine; N-(tert-Butoxycarbonyl)-α-methylalanine; N-(tert-Butyloxycarbonyl)-2-aminoisobutyric Acid; N-BOC-2-aminoisobutyric Acid; N-BOC-α-methylalanine; N-Boc-2,2-dimethylglycine; N-Boc-2-amino-2-methylpropanoic Acid; N-Boc-2-methylalanine; N-Boc-α,α-dimethylglycine; N-tert-Butoxycarbonyl-2-aminoisobutyric Acid; N-tert-Butoxycarbonyl-2-methylalanine; N-tert-Butoxycarbonyl-α-aminoisobutyric Acid; α-(Bocamino)isobutyric Acid. Grades: Highly Purified. CAS No. 30992-29-1. Pack Sizes: 10g. Molecular Formula: C9H17NO4, Molecular Weight: 203.24. US Biological Life Sciences. | Worldwide |
| Boc-D-His(Trt)-Aib-Gln(Trt)-Gly-OH | Boc-D-His(Trt)-Aib-Gln(Trt)-Gly-OH is a protected tetrapeptide used in peptide synthesis. The Boc (tert-Butoxycarbonyl) group protects the N-terminus of the D-histidine (D-His) residue, preventing it from reacting during synthesis. The Trt (Trityl) groups protect the side chains of both histidine and glutamine (Gln), shielding these functional groups until selective deprotection is performed. Aib (α-aminoisobutyric acid), known for inducing helical structures, is the third residue, and Gly (Glycine) is the final amino acid in the sequence, with a free carboxyl group at the C-terminus, indicated by -OH, allowing for further coupling or modifications. This peptide is used to incorporate D-histidine, Aib, and glutamine into peptides, with specific protections to ensure controlled synthesis and functional group reactivity. Synonyms: hXQG; N2-(2-((R)-2-((tert-Butoxycarbonyl)amino)-3-(1-trityl-1H-imidazol-4-yl)propanamido)-2-methylpropanoyl)-N5-trityl-L-glutaminylglycine. Grade: ≥99%. Molecular formula: C60H63N7O8. Mole weight: 1010.21. | |
| Boc-D-Tyr(OtBu)-Aib-Gln(Trt)-Gly-OH | Boc-D-Tyr(OtBu)-Aib-Gln(Trt)-Gly-OH is a protected tetrapeptide utilized in peptide synthesis. The Boc (tert-Butoxycarbonyl) group safeguards the N-terminus of the D-tyrosine (D-Tyr) residue, while the OtBu (tert-butyl) group protects the hydroxyl group on the D-tyrosine's side chain, preventing premature reactions during synthesis. The second residue, Aib (α-aminoisobutyric acid), is known for its ability to induce helical conformations in peptides. The Gln (Glutamine) residue has its side chain protected by a Trt (Trityl) group, allowing for selective deprotection later in the synthesis process. The final residue, Gly (Glycine), has a free carboxyl group at the C-terminus, denoted by -OH, which can be used for further coupling or modifications. This peptide is specifically designed to incorporate D-tyrosine, Aib, glutamine, and glycine into peptide structures, with carefully selected protective groups to ensure controlled and efficient synthesis. Synonyms: yXQG; N2-(2-((R)-3-(4-(tert-Butoxy)phenyl)-2-((tert-butoxycarbonyl)amino)propanamido)-2-methylpropanoyl)-N5-trityl-L-glutaminylglycine; Boc-D-Tyr(tBu)-Aib-Gln(Trt)-Gly-OH. Grade: ≥95%. Molecular formula: C48H59N5O9. Mole weight: 850.03. | |
| Boc-D-Tyr(OtBu)-Aib-Glu(OtBu)-Gly-OH | Boc-D-Tyr(OtBu)-Aib-Glu(OtBu)-Gly-OH is a protected tetrapeptide used in peptide synthesis. The Boc (tert-Butoxycarbonyl) group protects the N-terminus of the D-tyrosine (D-Tyr) residue, preventing it from reacting during synthesis. The side chain hydroxyl group of D-tyrosine and the carboxyl group of glutamic acid (Glu) are protected by OtBu (tert-butyl) groups, which shield these functional groups until selective deprotection is needed. Aib (α-aminoisobutyric acid), known for its ability to induce helical structures, is the third residue, and Gly (Glycine), the final amino acid, has a free carboxyl group at the C-terminus, indicated by -OH, allowing for further coupling or modifications. This peptide incorporates D-tyrosine, Aib, glutamic acid, and glycine into peptide sequences, with specific protections to ensure controlled and efficient synthesis. Synonyms: yXEG; ((S)-5-(tert-Butoxy)-2-(2-((R)-3-(4-(tert-Butoxy)phenyl)-2-((tert-butoxycarbonyl)amino)propanamido)-2-methylpropanamido)-5-oxopentanoyl)glycine; Boc-D-Tyr(tBu)-Aib-Glu(tBu)-Gly-OH. Grade: ≥90%. Molecular formula: C33H52N4O10. Mole weight: 664.80. | |
| Boc-D-Tyr(OtBu)-Aib-OH | Boc-D-Tyr(OtBu)-Aib-OH is a protected dipeptide used in peptide synthesis. The Boc (tert-Butoxycarbonyl) group protects the N-terminus of the D-tyrosine (D-Tyr) residue, preventing unwanted reactions during synthesis. The hydroxyl group on the D-tyrosine side chain is protected by an OtBu (tert-butyl) group, safeguarding it from reactivity until selective deprotection is desired. Aib (α-aminoisobutyric acid) is the second amino acid in the sequence, a non-natural amino acid known for inducing helical structures in peptides. The -OH at the C-terminus indicates a free carboxyl group, allowing for further peptide coupling. This compound is utilized to introduce D-tyrosine and Aib into peptides, with specific protections ensuring controlled and selective synthesis while incorporating structural constraints. Synonyms: Boc-D-Tyr(tBu)-Aib-OH; N-tert-Butoxycarbonyl-O4-tert-butyl-D-tyrosyl-alpha-methyl-alanine; (R)-2-(3-(4-(tert-Butoxy)phenyl)-2-((tert-butoxycarbonyl)amino)propanamido)-2-methylpropanoic acid. Grade: ≥95%. Molecular formula: C22H34N2O6. Mole weight: 422.52. | |
| Boc-His(Trt)-Aib-Gln(Trt)-Gly-Gly-OH | Boc-His(Trt)-Aib-Gln(Trt)-Gly-Gly-OH is a protected pentapeptide used in peptide synthesis. It includes histidine (His), α-aminoisobutyric acid (Aib), glutamine (Gln), and two glycine (Gly) residues. The Boc (tert-Butyloxycarbonyl) group protects the N-terminus of the histidine residue, while the Trt (Trityl) groups shield the side chains of histidine and glutamine, preventing premature reactions. The Aib residue adds conformational rigidity, and the two glycine residues at the C-terminus are free, indicated by -OH, allowing for further coupling or modifications. This peptide is designed to ensure controlled reactivity and stability throughout the synthesis process. Synonyms: HXQGG; N2-(2-((S)-2-((tert-Butoxycarbonyl)amino)-3-(1-trityl-1H-imidazol-4-yl)propanamido)-2-methylpropanoyl)-N5-trityl-L-glutaminylglycylglycine. Grade: ≥96%. Molecular formula: C62H66N8O9. Mole weight: 1067.26. | |
| Boc-His(Trt)-Aib-Gln(Trt)-OH | Boc-His(Trt)-Aib-Gln(Trt)-OH is a protected tripeptide used in peptide synthesis. The Boc (tert-Butoxycarbonyl) group protects the N-terminus of the histidine (His) residue, preventing it from reacting during synthesis. The side chain imidazole group of histidine and the amide group of glutamine (Gln) are protected by Trt (Trityl) groups, shielding these functional groups from unwanted reactions until selective deprotection is performed. Aib (α-aminoisobutyric acid), known for inducing helical structures, is the middle residue. The -OH at the C-terminus of glutamine indicates a free carboxyl group, allowing for further coupling or modifications. This peptide is used to incorporate histidine, Aib, and glutamine into peptides, with specific protections to ensure controlled and efficient peptide synthesis. Synonyms: HXQ; N2-(2-((S)-2-((tert-Butoxycarbonyl)amino)-3-(1-trityl-1H-imidazol-4-yl)propanamido)-2-methylpropanoyl)-N5-trityl-L-glutamine. Grade: ≥95%. Molecular formula: C58H60N6O7. Mole weight: 953.15. | |
| Boc-His(Trt)-Aib-Gly-OH | Boc-His(Trt)-Aib-Gly-OH is a protected tripeptide used in peptide synthesis. The Boc (tert-Butoxycarbonyl) group protects the N-terminus of the histidine (His) residue, preventing it from reacting during synthesis. The imidazole side chain of histidine is protected by a Trt (Trityl) group, which shields it from unwanted reactions until deprotection is performed. Aib (α-aminoisobutyric acid), known for its helical structure-inducing properties, is the middle residue. Gly (Glycine), the final amino acid, has a free carboxyl group at the C-terminus, indicated by -OH, allowing for further peptide coupling or modifications. This peptide is used to introduce histidine, Aib, and glycine into peptide sequences, with specific protections to ensure controlled and efficient peptide synthesis. Synonyms: HXG; (S)-(2-(2-((tert-Butoxycarbonyl)amino)-3-(1-trityl-1H-imidazol-4-yl)propanamido)-2-methylpropanoyl)glycine. Grade: ≥97%. Molecular formula: C36H41N5O6. Mole weight: 639.75. | |
| Boc-N-Me-Aib-OH | Boc-N-Me-Aib-OH. Synonyms: Boc-N-methyl-aminoisobutyric acid; N-Boc-N,2-dimethylalanine. CAS No. 146000-39-7. Molecular formula: C10H19NO4. Mole weight: 217.3. | |
| Boc-Tyr(OtBu)-Aib-Gln(Trt)-Gly-Gly-OH | Boc-Tyr(OtBu)-Aib-Gln(Trt)-Gly-Gly-OH is a protected pentapeptide used in peptide synthesis. The sequence comprises tyrosine (Tyr), α-aminoisobutyric acid (Aib), glutamine (Gln), and two glycine (Gly) residues. The Boc (tert-Butyloxycarbonyl) group protects the N-terminus of the tyrosine residue, while the OtBu (tert-butyl) group protects the hydroxyl group of tyrosine and the carboxyl group of glutamine. The Trt (Trityl) group shields the side chain of the glutamine residue, preventing it from reacting prematurely. The two glycine residues at the C-terminus are free, indicated by -OH, which facilitates further coupling or modifications. This peptide design ensures controlled reactivity and stability throughout synthesis, suitable for incorporation into larger peptide sequences. Synonyms: YXQGG; N2-(2-((S)-3-(4-(tert-Butoxy)phenyl)-2-((tert-butoxycarbonyl)amino)propanamido)-2-methylpropanoyl)-N5-trityl-L-glutaminylglycylglycine; Boc-Tyr(tBu)-Aib-Gln(Trt)-Gly-Gly-OH. Grade: ≥97%. Molecular formula: C50H62N6O10. Mole weight: 907.08. | |
| Boc-Tyr(OtBu)-Aib-Gln(Trt)-Gly-OH | Boc-Tyr(OtBu)-Aib-Gln(Trt)-Gly-OH is a protected tetrapeptide commonly used in peptide synthesis. The Boc (tert-Butoxycarbonyl) group protects the N-terminus of the tyrosine (Tyr) residue, while the OtBu (tert-butyl) group protects its side chain hydroxyl group, preventing premature reactions during synthesis. Aib (α-aminoisobutyric acid), a residue known for promoting helical structures, is the second amino acid in the sequence. The glutamine (Gln) residue has its side chain protected by a Trt (Trityl) group. The final amino acid, glycine (Gly), has a free carboxyl group at the C-terminus, indicated by -OH, which allows for further modifications or coupling reactions. This peptide is used to incorporate tyrosine, Aib, glutamine, and glycine into peptide chains, with strategic protection to ensure controlled and efficient synthesis. Synonyms: YXQG; N2-(2-((S)-3-(4-(tert-Butoxy)phenyl)-2-((tert-butoxycarbonyl)amino)propanamido)-2-methylpropanoyl)-N5-trityl-L-glutaminylglycine; Boc-Tyr(tBu)-Aib-Gln(Trt)-Gly-OH. Grade: ≥96%. CAS No. 2612237-79-1. Molecular formula: C48H59N5O9. Mole weight: 850.03. | |
| Boc-Tyr(OtBu)-Aib-Gln(Trt)-OH | Boc-Tyr(OtBu)-Aib-Gln(Trt)-OH is a protected tripeptide used in peptide synthesis. The Boc (tert-Butoxycarbonyl) group protects the N-terminus of the tyrosine (Tyr) residue, preventing it from reacting during synthesis. The hydroxyl group of tyrosine and the side chain amide group of glutamine (Gln) are protected by OtBu (tert-butyl) and Trt (Trityl) groups, respectively, which shield these functional groups from unwanted reactions until selective deprotection is performed. Aib (α-aminoisobutyric acid), known for its helical-inducing properties, is the middle residue in the sequence. The -OH at the C-terminus indicates a free carboxyl group, allowing for further coupling or modifications. This compound is used to incorporate tyrosine, Aib, and glutamine into peptides, with specific protections to ensure controlled and efficient peptide synthesis. Synonyms: YXQ; N2-(2-((S)-3-(4-(tert-Butoxy)phenyl)-2-((tert-butoxycarbonyl)amino)propanamido)-2-methylpropanoyl)-N5-trityl-L-glutamine; Boc-Tyr(tBu)-Aib-Gln(Trt)-OH. Grade: ≥97%. Molecular formula: C46H56N4O8. Mole weight: 792.97. | |
| Boc-Tyr(OtBu)-Aib-Glu(OtBu)-Gly-Gly-OH | Boc-Tyr(OtBu)-Aib-Glu(OtBu)-Gly-Gly-OH is a protected pentapeptide used in peptide synthesis. The sequence includes tyrosine (Tyr), α-aminoisobutyric acid (Aib), glutamic acid (Glu), and two glycine (Gly) residues. The Boc (tert-Butyloxycarbonyl) group protects the N-terminus of the tyrosine residue, while the OtBu (tert-butyl) groups protect the hydroxyl groups of the tyrosine and glutamic acid residues. The Aib is a non-standard amino acid that enhances conformational rigidity. The two glycine residues at the C-terminus are free, indicated by -OH, allowing for further coupling or modifications. This peptide is designed to be incorporated into larger peptide sequences, with the protective groups ensuring controlled reactivity and stability throughout the synthesis process. Synonyms: YXEGG; ((S)-5-(tert-Butoxy)-2-(2-((S)-3-(4-(tert-butoxy)phenyl)-2-((tert-butoxycarbonyl)amino)propanamido)-2-methylpropanamido)-5-oxopentanoyl)glycylglycine; Boc-Tyr(tBu)-Aib-Glu(tBu)-Gly-Gly-OH. Grade: ≥95%. Molecular formula: C35H55N5O11. Mole weight: 721.85. | |
| Boc-Tyr(OtBu)-Aib-Glu(OtBu)-Gly-OH | Boc-Tyr(OtBu)-Aib-Glu(OtBu)-Gly-OH is a protected tetrapeptide used in peptide synthesis. The Boc (tert-Butoxycarbonyl) group protects the N-terminus of the tyrosine (Tyr) residue, preventing it from reacting during synthesis. The side chain hydroxyl group of tyrosine and the carboxyl group of glutamic acid (Glu) are protected by OtBu (tert-butyl) groups, which shield these functional groups until deprotection. Aib (α-aminoisobutyric acid), known for inducing helical structures, is the third residue, and Gly (Glycine), the final amino acid, has a free carboxyl group at the C-terminus, indicated by -OH, allowing for further peptide coupling or modifications. This peptide is used to incorporate tyrosine, Aib, glutamic acid, and glycine into peptide sequences, with specific protections to ensure controlled and efficient synthesis. Synonyms: YXEG; ((S)-5-(tert-Butoxy)-2-(2-((S)-3-(4-(tert-butoxy)phenyl)-2-((tert-butoxycarbonyl)amino)propanamido)-2-methylpropanamido)-5-oxopentanoyl)glycine; Boc-Tyr(tBu)-Aib-Glu(tBu)-Gly-OH; Boc-Tyr(tBu)-Ala(αMe)-Glu(tBu)-Gly-OH; Boc-Tyr(tBu)-Aib-Glu(OtBu)-Gly-OH. Grade: ≥95%. CAS No. 2682040-93-1. Molecular formula: C33H52N4O10. Mole weight: 664.80. | |
| Boc-Tyr(OtBu)-Aib-Glu(OtBu)-Gly-Thr(OtBu)-Phe-Thr(OtBu)-OH | Boc-Tyr(OtBu)-Aib-Glu(OtBu)-Gly-Thr(OtBu)-Phe-Thr(OtBu)-OH is a protected heptapeptide used in peptide synthesis. It includes tyrosine (Tyr), α-aminoisobutyric acid (Aib), glutamic acid (Glu), glycine (Gly), threonine (Thr), and phenylalanine (Phe), with Boc (tert-Butyloxycarbonyl) and OtBu (tert-butyl) groups protecting the amino and hydroxyl groups, respectively. The peptide has a free -OH group at the C-terminus for further modifications or coupling. This octapeptide is designed for controlled reactivity and stability, making it suitable for synthesis and applications in peptide-based drug design and functional studies. Synonyms: Boc-Tyr(OtBu)-Aib-Glu(OtBu)-Gly-Thr(OtBu)-Phe-Thr(OtBu); N-N-(((S)-5-(tert-Butoxy)-2-(2-((S)-3-(4-(tert-butoxy)phenyl)-2-((tert-butoxycarbonyl)amino)propanamido)-2-methylpropanamido)-5-oxopentanoyl)glycyl)-O-(tert-butyl)-L-threonyl-L-phenylalanyl-O-(tert-butyl)-L-threonine; Boc-Tyr(tBu)-Aib-Glu(tBu)-Gly-Thr(tBu)-Phe-Thr(tBu)-OH. Grade: ≥90%. Molecular formula: C58H91N7O15. Mole weight: 1126.40. | |
| Boc-Tyr(OtBu)-Aib-Glu(OtBu)-Gly-Thr(OtBu)-Phe-Thr(OtBu)-Ser(OtBu)-Asp(OtBu)-Tyr(OtBu)-Ser(OtBu)-Ile-Aib-Leu-OH | Boc-Tyr(OtBu)-Aib-Glu(OtBu)-Gly-Thr(OtBu)-Phe-Thr(OtBu)-Ser(OtBu)-Asp(OtBu)-Tyr(OtBu)-Ser(OtBu)-Ile-Aib-Leu-OH is a protected tetradecapeptide consisting of 14 amino acids. The peptide features Boc (tert-butoxycarbonyl) and OtBu (tert-butyl) protecting groups on residues like tyrosine (Tyr), threonine (Thr), serine (Ser), aspartic acid (Asp), and glutamic acid (Glu), while Aib represents α-aminoisobutyric acid. This peptide, with a free carboxyl end (-OH), is useful in various biochemical studies, such as exploring protein structure, receptor binding, or therapeutic development. Synonyms: Boc-Tyr(OtBu)-Aib-Glu(OtBu)-Gly-Thr(OtBu)-Phe-Thr(OtBu)-Ser(OtBu)-Asp(OtBu)-Tyr(OtBu)-Ser(OtBu)-Ile-Aib-Leu; (2-((2S,3S)-2-((S)-3-(tert-Butoxy)-2-((S)-2-((S)-4-(tert-butoxy)-2-((S)-3-(tert-butoxy)-2-((2S,3R)-3-(tert-butoxy)-2-((S)-2-((2S,3R)-3-(tert-butoxy)-2-(2-((S)-5-(tert-butoxy)-2-(2-((S)-3-(4-(tert-butoxy)phenyl)-2-((tert-butoxycarbonyl)amino)propanamido)-2-methylpropanamido)-5-oxopentanamido. Grade: ≥96%. Molecular formula: C109H176N14O27. Mole weight: 2114.68. | |
| Boc-Tyr(OtBu)-Aib-Glu(OtBu)-OH | Boc-Tyr(OtBu)-Aib-Glu(OtBu)-OH is a protected tripeptide used in peptide synthesis. The Boc (tert-Butoxycarbonyl) group protects the N-terminus of the tyrosine (Tyr) residue, preventing it from reacting during the synthesis. The hydroxyl group of tyrosine and the side chain carboxyl group of glutamic acid (Glu) are protected by OtBu (tert-butyl) groups, which shield these functional groups from reactivity until deprotection is performed. Aib (α-aminoisobutyric acid), known for its ability to induce helical structures, is the middle residue in the sequence. The -OH at the C-terminus indicates a free carboxyl group, allowing for further peptide coupling or modifications. This peptide is utilized to incorporate tyrosine, Aib, and glutamic acid into peptides while maintaining precise control over the reactivity of the functional groups through specific protections. Synonyms: YXE; (6S,12S)-12-(3-(tert-Butoxy)-3-oxopropyl)-6-(4-(tert-butoxy)benzyl)-2,2,9,9-tetramethyl-4,7,10-trioxo-3-oxa-5,8,11-triazatridecan-13-oic acid; Boc-Tyr(tBu)-Aib-Glu(tBu)-OH. Grade: ≥95%. Molecular formula: C31H49N3O9. Mole weight: 607.75. | |
| Boc-Tyr(OtBu)-Aib-Gly-OH | Boc-Tyr(OtBu)-Aib-Gly-OH is a protected tripeptide used in peptide synthesis. The Boc (tert-Butoxycarbonyl) group protects the N-terminus of the tyrosine (Tyr) residue, preventing it from reacting during synthesis. The hydroxyl group of tyrosine is protected by an OtBu (tert-butyl) group, which keeps it from reacting until deprotection is needed. Aib (α-aminoisobutyric acid), a non-natural amino acid known for inducing helical structures, follows tyrosine. Gly (Glycine), the final amino acid in the sequence, has a free carboxyl group at the C-terminus, indicated by -OH, allowing for further coupling or modifications. This compound is used to introduce tyrosine, Aib, and glycine into peptides, with selective protection of functional groups to ensure controlled and efficient peptide synthesis. Synonyms: YXG; (S)-(2-(3-(4-(tert-Butoxy)phenyl)-2-((tert-butoxycarbonyl)amino)propanamido)-2-methylpropanoyl)glycine. Grade: ≥99%. Molecular formula: C24H37N3O7. Mole weight: 479.57. | |
| Boc-Tyr(OtBu)-Aib-OH | Boc-Tyr(OtBu)-Aib-OH is a protected dipeptide used in peptide synthesis. The Boc (tert-Butoxycarbonyl) group protects the N-terminus of the tyrosine (Tyr) residue, preventing it from reacting during peptide assembly. The hydroxyl group on the tyrosine side chain is also protected by a tBu (tert-butyl) group, ensuring that it remains unreactive until the desired deprotection step. Aib (α-aminoisobutyric acid) is the second amino acid in the sequence, a non-natural amino acid known for inducing helical structures in peptides. The -OH at the C-terminus indicates a free carboxyl group, allowing for further peptide coupling. This compound is used to incorporate tyrosine and Aib into peptides, offering specific protective strategies for controlled synthesis and the introduction of conformational constraints. Synonyms: Boc-Tyr(tBu)-Aib-OH; N-tert-Butoxycarbonyl-O4-tert-butyl-L-tyrosyl-alpha-methyl-alanine; (S)-2-(3-(4-(tert-Butoxy)phenyl)-2-((tert-butoxycarbonyl)amino)propanamido)-2-methylpropanoic acid. Grade: ≥95%. CAS No. 2639221-78-4. Molecular formula: C22H34N2O6. Mole weight: 422.52. | |
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