Molecular structure of Isopropylamine, CAS Number: 75-31-0
Isopropylamine (CAS 75-31-0)
Alternate Names:
2-Aminopropane
CAS Number:
75-31-0
Purity:
≥99%
Molecular Weight:
59.11
Molecular Formula:
C3H9N
Supplemental Information:
This is classified as a Dangerous Good for transport and may be subject to additional shipping charges.
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.
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Isopropylamine serves as an intermediate in the synthesis of diverse chemicals. Notably, it plays a key role in producing other amines like diethylamine and triethylamine. Its versatility as a reagent in organic synthesis makes it a valuable building block for various compounds. Additionally, isopropylamine functions as an effective catalyst during the synthesis of organic substances and is an essential reagent in the production of peptides and polymers.
Isopropylamine (CAS 75-31-0) References
- Transformation of isopropylamine to L-alaninol by Pseudomonas sp. strain KIE171 involves N-glutamylated intermediates. | de Azevedo Wäsch, SI., et al. 2002. Appl Environ Microbiol. 68: 2368-75. PMID: 11976110
- The toxicity of Roundup® 360 SL formulation and its main constituents: glyphosate and isopropylamine towards non-target water photoautotrophs. | Lipok, J., et al. 2010. Ecotoxicol Environ Saf. 73: 1681-8. PMID: 20813408
- Combined use of isopropylamine and trifluoroacetic acid in methanol-containing mobile phases for chiral supercritical fluid chromatography. | De Klerck, K., et al. 2012. J Chromatogr A. 1234: 72-9. PMID: 22142971
- ω-Transaminase-catalyzed asymmetric synthesis of unnatural amino acids using isopropylamine as an amino donor. | Park, ES., et al. 2013. Org Biomol Chem. 11: 6929-33. PMID: 23897436
- Immobilization of (R)- and (S)-amine transaminases on chitosan support and their application for amine synthesis using isopropylamine as donor. | Mallin, H., et al. 2014. J Biotechnol. 191: 32-7. PMID: 24874095
- Skin Notations for Low-Molecular-Weight Amines: Development of a Testing Protocol with Isopropylamine as an Example. | Thredgold, L., et al. 2018. Ann Work Expo Health. 62: 633-638. PMID: 29846518
- The challenge of using isopropylamine as an amine donor in transaminase catalysed reactions. | Kelefiotis-Stratidakis, P., et al. 2019. Org Biomol Chem. 17: 1634-1642. PMID: 30394478
- Isobutylamine, Isopropylamine, sec-Butylamine, Propylamine, Hexylamine, Pentylamine and 2-Methylbutylamine (Flavoring Substances). | ,. 2019. Food Saf (Tokyo). 7: 54-55. PMID: 31998587
- Regioselective α-Deuteration of Michael Acceptors Mediated by Isopropylamine in D2O/AcOD. | Landge, VG., et al. 2020. Org Lett. 22: 9745-9750. PMID: 33259211
- Amine Volatilization from Herbicide Salts: Implications for Herbicide Formulations and Atmospheric Chemistry. | Sharkey, SM., et al. 2022. Environ Sci Technol. 56: 13644-13653. PMID: 36150089
- Isopropylamine, a biologically active deamination product of propranolol in dogs: identification of deuterated and unlabeled isopropylamine by gas chromatography-mass spectrometry. | Walle, T., et al. 1972. J Pharmacol Exp Ther. 183: 508-12. PMID: 4636389
- Nicotinic-like effects and tissue disposition of isopropylamine. | Privitera, PJ., et al. 1982. J Pharmacol Exp Ther. 222: 116-21. PMID: 7086693
- Toxicity studies in fertilized zebrafish eggs treated with N-methylamine, N,N-dimethylamine, 2-aminoethanol, isopropylamine, aniline, N-methylaniline, N,N-dimethylaniline, quinone, chloroacetaldehyde, or cyclohexanol. | Groth, G., et al. 1993. Bull Environ Contam Toxicol. 50: 878-82. PMID: 8495065
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
Isopropylamine, 25 ml | sc-250201 | 25 ml | $26.00 | |||
Isopropylamine, 250 ml | sc-250201A | 250 ml | $36.00 |