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蒸汽壓力
3.6 mmHg ( 20 °C)
品質等級
化驗
99%
自燃溫度
419 °F
折射率
n20/D 1.454 (lit.)
bp
158-159 °C (lit.)
密度
0.849 g/mL at 25 °C (lit.)
官能基
amine
SMILES 字串
CN(C)C1CCCCC1
InChI
1S/C8H17N/c1-9(2)8-6-4-3-5-7-8/h8H,3-7H2,1-2H3
InChI 密鑰
SVYKKECYCPFKGB-UHFFFAOYSA-N
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一般說明
空气中 N,N-二甲基环己基胺的采样和后续分析测定已有报道 。
應用
N , N -二甲基环己基胺已用于:
- 作为可切换的亲水性溶剂 (SHS),用于从冷冻干燥的 布氏葡萄球菌 微藻中提取脂质,用于生物燃料生产
- 作为水中三组分有机催化 Strecker 反应的催化剂
訊號詞
Danger
危險分類
Acute Tox. 2 Inhalation - Acute Tox. 3 Dermal - Acute Tox. 4 Oral - Aquatic Acute 1 - Flam. Liq. 3 - Skin Corr. 1B
儲存類別代碼
3 - Flammable liquids
水污染物質分類(WGK)
WGK 3
閃點(°F)
102.2 °F - closed cup
閃點(°C)
39 °C - closed cup
個人防護裝備
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
其他客户在看
Guillermo Lasarte-Aragonés et al.
Molecules (Basel, Switzerland), 25(1) (2019-12-29)
In the present work, the effectiveness of switchable hydrophobicity solvents (SHSs) as extraction solvent (N,N-Dimethylcyclohexylamine (DMCA), N,N-Diethylethanamine (TEA), and N,N-Benzyldimethylamine (DMBA)) for a variety of emerging pollutants was evaluated. Different pharmaceutical products (nonsteroidal anti-inflammatory drugs (NSAIDs), hormones, and triclosan) were
[Toxic properties of dimethylcyclohexylamine].
E S Smirnova et al.
Gigiena truda i professional'nye zabolevaniia, (5)(5), 54-55 (1984-05-01)
Alaina R Boyd et al.
Bioresource technology, 118, 628-632 (2012-06-23)
A switchable hydrophilicity solvent (SHS) was studied for its effectiveness at extracting lipids from freeze-dried samples of Botryococcus braunii microalgae. The SHS N,N-dimethylcyclohexylamine extracted up to 22 wt.% crude lipid relative to the freeze-dried cell weight. The solvent was removed
Joël Reignier et al.
Journal of colloid and interface science, 552, 153-165 (2019-05-28)
This paper presents an investigation of the morphology of growing polyurethane (PU) rigid foams during the very first seconds of the process by cryogenic scanning electron microscopy (cryo-SEM) performed at -150 °C. The heterogeneous nature of the initial mixture has been
Fabio Cruz-Acosta et al.
Chemical communications (Cambridge, England), (44)(44), 6839-6841 (2009-11-04)
The first three-component organocatalyzed Strecker reaction operating on water has been developed. The manifold utilizes ketones (aldehydes) as the starting carbonyl component, aniline as the primary amine, acetyl cyanide as the cyanide source and N,N-dimethylcyclohexylamine as the catalyst.
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