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品質水準
アッセイ
96%
フォーム
liquid
不純物
<4% 2-ethylhexanoic acid
屈折率
n20/D 1.415 (lit.)
bp
55 °C/13.5 mmHg (lit.)
密度
0.822 g/mL at 25 °C (lit.)
SMILES記法
[H]C(=O)C(CC)CCCC
InChI
1S/C8H16O/c1-3-5-6-8(4-2)7-9/h7-8H,3-6H2,1-2H3
InChI Key
LGYNIFWIKSEESD-UHFFFAOYSA-N
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関連するカテゴリー
詳細
2-Ethylhexanal is an aliphatic aldehyde used as an intermediate to produce various useful products such as perfumes, disinfectants, paints, warning agents, insecticides, and leak detectors.
アプリケーション
2-Ethylhexanal can be used as:
- A reductant in the Mukaiyama epoxidation of cis-cyclooctene.
- A reactant in the Horner-Wadsworth-Emmons reaction to synthesize cis-α,β-unsaturated amides.
- A starting material to synthesize 2-ethylhexanoic acid using manganese(II) acetate as a catalyst.
シグナルワード
Warning
危険有害性情報
危険有害性の分類
Flam. Liq. 3 - Repr. 2 - Skin Sens. 1
保管分類コード
3 - Flammable liquids
WGK
WGK 1
引火点(°F)
111.2 °F - closed cup
引火点(℃)
44 °C - closed cup
個人用保護具 (PPE)
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
適用法令
試験研究用途を考慮した関連法令を主に挙げております。化学物質以外については、一部の情報のみ提供しています。 製品を安全かつ合法的に使用することは、使用者の義務です。最新情報により修正される場合があります。WEBの反映には時間を要することがあるため、適宜SDSをご参照ください。
消防法
第4類:引火性液体
第二石油類
危険等級III
非水溶性液体
Jan Code
E29109-5ML:
E29109-VAR:
E29109-1L:
E29109-BULK:
E29109-250ML:
E29109-10KG:
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Factors affecting the selectivity of air oxidation of 2-ethyhexanal, an α-branched aliphatic aldehyde
Lehtinen C and Brunow G
Organic Process Research & Development, 4, 544-549 (2000)
David M Hodgson et al.
The Journal of organic chemistry, 78(4), 1508-1518 (2013-01-30)
The synthesis and alkylation of chiral, nonracemic tropane- and homotropane-derived enamines is examined as an approach to enantioenriched α-alkylated aldehydes. The two bicyclic N auxiliaries, which differ by a single methylene group, give opposite senses of asymmetric induction on alkylation
The effect of feeding di-(2-ethylhexyl) phthalate and related compounds on lipids in the laying hen.
D L Wood et al.
Poultry science, 63(3), 469-477 (1984-03-01)
Di-(2-ethylhexyl) phthalate (DEHP) and three structurally related side-chain analogs were fed to laying hens to determine relationships of structure to effects on lipid metabolism. Hubbard broiler breeder hens were fed either a standard laying mash control diet or the control
G Casperson et al.
Journal of basic microbiology, 26(5), 259-269 (1986-01-01)
Analogs of the natural substance (E)-hex-2-en-1-al which occurs naturally in green plants and is known to have microbiocidal properties were synthesized and studied with respect to their antifungal properties. Saturated and unsaturated aldehydes, alcohols, carbon acids and enolacetate were tested
Heather L Voegtle et al.
Journal of chemical ecology, 34(2), 215-219 (2008-01-24)
E-2-ethyl-2-hexen-1-ol (1), mellein (4), and 4-hydroxymellein (5) were identified as the major volatile compounds in the head and/or thorax of Camponotus quadrisectus. Neither 1 nor 5 have been previously detected in insects. Also identified were small amounts of m-cresol (2)
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