推荐产品
生物源
synthetic
品質等級
等級
FG
Kosher
法律遵循
EU Regulation 1334/2008 & 872/2012
蒸汽壓力
1.4 mmHg ( 20 °C)
化驗
≥98%
expl. lim.
16.3 %
折射率
n20/D 1.443 (lit.)
bp
140 °C (lit.)
密度
0.848 g/mL at 25 °C (lit.)
應用
flavors and fragrances
文件
see Safety & Documentation for available documents
食物過敏原
no known allergens
感官的
green; fruity
SMILES 字串
C\C(C)=C\CO
InChI
1S/C5H10O/c1-5(2)3-4-6/h3,6H,4H2,1-2H3
InChI 密鑰
ASUAYTHWZCLXAN-UHFFFAOYSA-N
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一般說明
甲基-2-丁烯-1-醇是人参果和水仙花的关键挥发性香气成分之一。它被用作香料化妆品、家庭清洁剂和洗涤剂中的香料成分。
訊號詞
Danger
危險分類
Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Eye Dam. 1 - Flam. Liq. 3 - Skin Corr. 1B - STOT SE 3
標靶器官
Respiratory system
儲存類別代碼
3 - Flammable liquids
水污染物質分類(WGK)
WGK 1
閃點(°F)
124.7 °F - closed cup
閃點(°C)
51.5 °C - closed cup
個人防護裝備
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
其他客户在看
Use of solid-phase microextraction as a sampling technique for the characterization of volatile compounds emitted from Chinese daffodil flowers.
Journal of Analytical Chemistry, 62(7), 674-679 (2007)
Fragrance material review on 3-methyl-2-buten-1-ol.
Food And Chemical Toxicology, 48, S64-S69 (2010)
Quantitative analysis of the volatile aroma components of pepino fruit by purge?and?trap and gas chromatography.
Journal of the Science of Food and Agriculture, 82(10), 1182-1188 (2002)
Journal of chromatography. A, 967(1), 21-55 (2002-09-11)
The chemical analysis and quality control of Ginkgo leaves and extracts is reviewed. Important constituents present in the medicinally used leaves are the terpene trilactones, i.e., ginkgolides A, B, C, J and bilobalide, many flavonol glycosides, biflavones, proanthocyanidins, alkylphenols, simple
Journal of the American Chemical Society, 134(33), 13881-13888 (2012-08-07)
We describe a practical, multigram synthesis of (2Z,6Z,10Z,14Z,18E,22E)-3,7,11,15,19,23,27-heptamethyl-2,6,10,14,18,22,26-octacosaheptaen-1-ol [(Z(4),E(2),ω)-heptaprenol, 4] using the nerol-derived sulfone 8 as the key intermediate. Sulfone 8 is prepared by the literature route and is converted in five additional steps (18% yield from 8) to (Z(4),E(2),ω)-heptaprenol
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