2-Amino-3-methyl-1-butanol - CAS 16369-05-4
Catalog: |
BB012024 |
Product Name: |
2-Amino-3-methyl-1-butanol |
CAS: |
16369-05-4 |
Synonyms: |
2-amino-3-methylbutan-1-ol |
IUPAC Name: | 2-amino-3-methylbutan-1-ol |
Description: | 2-Amino-3-methyl-1-butanol (CAS# 16369-05-4) is an inhibitor of myoblast protein synthesis. A useful research chemical. |
Molecular Weight: | 103.16 |
Molecular Formula: | C5H13NO |
Canonical SMILES: | CC(C)C(CO)N |
InChI: | InChI=1S/C5H13NO/c1-4(2)5(6)3-7/h4-5,7H,3,6H2,1-2H3 |
InChI Key: | NWYYWIJOWOLJNR-UHFFFAOYSA-N |
Boiling Point: | 75-77 ℃ (8 torr) |
Purity: | ≥ 99 % |
Density: | 0.936 g/mL at 25 ℃ (lit.) |
Appearance: | White crystalline powder |
Storage: | Refrigerator (+4 ℃) |
MDL: | MFCD00004730 |
LogP: | 0.66230 |
GHS Hazard Statement: | H315 (100%): Causes skin irritation [Warning Skin corrosion/irritation] |
Precautionary Statement: | P261, P264, P271, P280, P302+P352, P304+P340, P305+P351+P338, P312, P321, P332+P313, P337+P313, P362, P403+P233, P405, and P501 |
Signal Word: | Warning |
Publication Number | Title | Priority Date |
WO-2020186126-A1 | Multi-amine polyester dispersant made via an anhydride intermediate | 20190314 |
WO-2020186133-A1 | Multi-amine dispersant made via an anhydride intermediate | 20190314 |
WO-2020150384-A1 | Method of strengthening non-keratinous fibers, and uses thereof | 20190117 |
WO-2020087901-A1 | Rho kinase inhibitor, method for preparing same and uses thereof | 20181030 |
EP-3878846-A1 | Rho kinase inhibitor, method for preparing same and uses thereof | 20181030 |
PMID | Publication Date | Title | Journal |
21476502 | 20110520 | Synthesis, conformational stability, and asymmetric transformation of atropisomeric 1,8-bisphenolnaphthalenes | The Journal of organic chemistry |
21416080 | 20110514 | Palladacycles of novel bisoxazoline chelating ligands based on the dimeric cyclobutadiene linked cobalt sandwich compound [(η5-Cp)Co(η4-C4Ph3)]2 | Dalton transactions (Cambridge, England : 2003) |
21077217 | 20101201 | β-Amino alcohol selectors for enantioselective separation of amino acids by ligand-exchange capillary zone electrophoresis in a low molecular weight organogel | Electrophoresis |
19799603 | 20100301 | Amino acid derivatives from Lucilia sericata excretions/secretions may contribute to the beneficial effects of maggot therapy via increased angiogenesis | The British journal of dermatology |
19586009 | 20090821 | Synthesis of highly enantioenriched chiral alpha-aminoorganotins via diastereoselective ring opening of chiral N-(arenesulfonyl) 2-tributylstannyloxazolidines | The Journal of organic chemistry |
Complexity: | 45.3 |
Compound Is Canonicalized: | Yes |
Covalently-Bonded Unit Count: | 1 |
Defined Atom Stereocenter Count: | 0 |
Defined Bond Stereocenter Count: | 0 |
Exact Mass: | 103.099714038 |
Formal Charge: | 0 |
Heavy Atom Count: | 7 |
Hydrogen Bond Acceptor Count: | 2 |
Hydrogen Bond Donor Count: | 2 |
Isotope Atom Count: | 0 |
Monoisotopic Mass: | 103.099714038 |
Rotatable Bond Count: | 2 |
Topological Polar Surface Area: | 46.2 Å2 |
Undefined Atom Stereocenter Count: | 1 |
Undefined Bond Stereocenter Count: | 0 |
XLogP3: | 0 |
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