모든 사진(2)
About This Item
Linear Formula:
CH3CH=CHCH=CHCHO
CAS Number:
Molecular Weight:
96.13
Beilstein:
1698401
EC Number:
MDL number:
UNSPSC 코드:
12352100
PubChem Substance ID:
NACRES:
NA.22
추천 제품
vapor density
>1 (vs air)
분석
95%
형태
liquid
refractive index
n20/D 1.541 (lit.)
bp
69 °C/20 mmHg (lit.)
density
0.895 g/mL at 20 °C
0.871 g/mL at 25 °C (lit.)
저장 온도
2-8°C
SMILES string
[H]C(=O)\C=C\C=C\C
InChI
1S/C6H8O/c1-2-3-4-5-6-7/h2-6H,1H3/b3-2+,5-4+
InChI key
BATOPAZDIZEVQF-MQQKCMAXSA-N
유사한 제품을 찾으십니까? 방문 제품 비교 안내
일반 설명
trans,trans-2,4-Hexadienal is an α,β-unsaturated aldehyde used as a food additive and as a starting material in various chemical and pharmaceutical industries.
애플리케이션
trans,trans-2,4-Hexadienal (sorbic aldehyde) was used in the synthesis of chiral cycloadducts.
신호어
Danger
유해 및 위험 성명서
Hazard Classifications
Acute Tox. 3 Dermal - Acute Tox. 3 Oral - Eye Dam. 1 - Skin Corr. 1B - Skin Sens. 1
Storage Class Code
6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
WGK
WGK 3
Flash Point (°F)
154.0 °F - closed cup
Flash Point (°C)
67.77 °C - closed cup
개인 보호 장비
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
시험 성적서(COA)
제품의 로트/배치 번호를 입력하여 시험 성적서(COA)을 검색하십시오. 로트 및 배치 번호는 제품 라벨에 있는 ‘로트’ 또는 ‘배치’라는 용어 뒤에서 찾을 수 있습니다.
이미 열람한 고객
De novo asymmetric synthesis of two 5-amino-5, 6-dideoxy-D-allose derivatives.
Tetrahedron Letters, 35(31), 5653-5656 (1994)
Atmospheric reactions between E, E-2, 4-hexadienal and OH, NO3 radicals and Cl atoms
Colmenar, et al.
Atmospheric Environment, 99, 159-167 (2014)
Influence of 1-butanethiol and metal ions on hydrogenation of trans, trans-2, 4-hexadienal at platinum nanocatalysts
Du, YK and Xu, et al.
Colloids and Surfaces. A, Physicochemical and Engineering Aspects, 257, 75-78 (2005)
Margaret P O'Connor et al.
Physical chemistry chemical physics : PCCP, 8(44), 5236-5246 (2007-01-05)
The atmospheric photolysis of E-2-hexenal, Z-3-hexenal and E,E-2,4-hexadienal has been investigated at the large outdoor European Photoreactor (EUPHORE) in Valencia, Spain. E-2-Hexenal and E,E-2,4-hexadienal were found to undergo rapid isomerization to produce Z-2-hexenal and a ketene-type compound (probably E-hexa-1,3-dien-1-one), respectively.
Po C Chan et al.
Archives of toxicology, 77(9), 511-520 (2003-07-25)
2,4-Hexadienal (2,4-Hx) was studied for its toxicity and carcinogenicity because of its alpha, beta-unsaturated aldehyde structure and potential link between exposure to lipid peroxidation products in the diet and human malignancies. Male and female F344N rats and B6C3F1 mice received
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