6728-26-3
Chemical Structure
trans-2-Hexenal
Synonym(s): (E)-2-Hexenal
- CAS No.: 6728-26-3
- Formula:C6H10O
- Molecular Weight:98.15
IUPAC Name: (E)-hex-2-enal
InChIKey: MBDOYVRWFFCFHM-SNAWJCMRSA-N
SMILES: CCC/C=C/C=O
Biological Activity: trans-2-Hexenal ((E)-2-Hexenal) is a volatile compound widely present in fresh plants, vegetables, and fruits, with a unique leafy aroma. trans-2-Hexenal has antifungal activity and can also inhibit the germination of soybean seeds and the growth of seedlings. In addition, trans-2-Hexenal can be used to determine low-molecular-weight carbonyl compounds that are reactive with biological nucleophiles in biological samples[1][2][3][4].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
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trans-2-Hexenal | 99.65% | trans-2-Hexenal ((E)-2-Hexenal) is a volatile compound widely present in fresh plants, vegetables, and fruits, with a unique leafy aroma. trans-2-Hexenal has antifungal activity and can also inhibit the germination of soybean seeds and the growth of seedlings. In addition, trans-2-Hexenal can be used to determine low-molecular-weight carbonyl compounds that are reactive with biological nucleophiles in biological samples. | ||||||||||||||||||||
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Trans-2-Hexenal (Standard) | 99.90% | Trans-2-Hexenal (Standard) is the analytical standard of Trans-2-Hexenal. This product is intended for research and analytical applications. Trans-2-Hexenal can be used for the determination of low-molecular-weight carbonyl compounds which are reactive with biological nucleophiles in biological samples. | ||||||||||||||||||||
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trans-2-Hexenal-d2-1 | trans-2-Hexenal-d2-1 is the deuterium labeled trans-2-Hexenal (HY-128429). trans-2-Hexenal ((E)-2-Hexenal) is a volatile compound widely present in fresh plants, vegetables, and fruits, with a unique leafy aroma. trans-2-Hexenal has antifungal activity and can also inhibit the germination of soybean seeds and the growth of seedlings. In addition, trans-2-Hexenal can be used to determine low-molecular-weight carbonyl compounds that are reactive with biological nucleophiles in biological samples. | |||||||||||||||||||||
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- [1]. Konidari CN, et al. Determination of plasma, urine, and bovine serum albumin low-molecular-weight carbonyl levels by capillary gas chromatography with electron-capture and mass-selective detection.Anal Biochem. 2005 Mar 1;338(1):62-70. [Content Brief]
- [2]. Gardner H W, et al. Hexanal, trans-2-hexenal, and trans-2-nonenal inhibit soybean, Glycine max, seed germination. Journal of Agricultural and Food Chemistry, 1990, 38(6): 1316-1320.
- [3]. Zhang J, et al. Antifungal activity of trans‐2‐hexenal against Penicillium cyclopium by a membrane damage mechanism. Journal of Food Biochemistry, 2017, 41(2): e12289.
- [4]. Hatanaka A, et al. Formation of cis-3-hexenal, trans-2-hexenal and cis-3-hexenol in macerated Thea sinensis leaves. Phytochemistry, 1973, 12(10): 2341-2346.
