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Merck

29135

Supelco

环己酮

Selectophore, ≥99.5%

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About This Item

线性分子式:
C6H10(=O)
CAS号:
分子量:
98.14
Beilstein:
385735
EC號碼:
MDL號碼:
分類程式碼代碼:
26111700
PubChem物質ID:
NACRES:
NB.61

等級

for ion-selective electrodes

品質等級

蒸汽密度

3.4 (vs air)

蒸汽壓力

3.4 mmHg ( 20 °C)

描述

solvent for preparation of membranes

產品線

Selectophore

化驗

≥99.5% (GC)
≥99.5%

自燃溫度

788 °F

expl. lim.

1.1 %, 100 °F
9.4 %

雜質

≤0.1% water

折射率

n20/D 1.450 (lit.)
n20/D 1.451

bp

155 °C (lit.)

mp

−47 °C (lit.)

密度

0.947 g/mL at 25 °C (lit.)

SMILES 字串

O=C1CCCCC1

InChI

1S/C6H10O/c7-6-4-2-1-3-5-6/h1-5H2

InChI 密鑰

JHIVVAPYMSGYDF-UHFFFAOYSA-N

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一般說明

环己酮是工业上重要的试剂。也是合成尼龙的主要中间体。
请访问我们的 传感器应用门户 网站,了解更多信息。

其他說明

用于制备微电极离子选择性膜的溶剂;比其他溶剂的挥发性低

法律資訊

Selectophore is a trademark of Merck KGaA, Darmstadt, Germany

訊號詞

Danger

危險分類

Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Eye Dam. 1 - Flam. Liq. 3 - Skin Irrit. 2 - 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)

111.2 °F - closed cup

閃點(°C)

44 °C - closed cup

個人防護裝備

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter


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Selective phenol hydrogenation to cyclohexanone over a dual supported Pd-Lewis acid catalyst.
Liu H
Science, 326 (5957), 1250-1252 (2009)
Effect of hydrogen sulphide on the hydrodeoxygenation of aromatic and aliphatic oxygenates on sulphided catalysts.
Senol OI
J. Mol. Catal. A: Chem., 277 (1), 107-112 (2007)
U. Schaller et al.
Pflugers Archiv : European Journal of Physiology (1993)
Alakananda Hajra et al.
Organic letters, 14(21), 5488-5491 (2012-10-18)
Dehydrogenative aromatization of cyclohexanone imines to arylamines has been achieved using a palladium catalyst under aerobic conditions. The reaction is applicable to a variety of imines that are either preformed or generated in situ from cyclohexanone derivatives and aryl or
Brahm J Yachnin et al.
Journal of the American Chemical Society, 134(18), 7788-7795 (2012-04-18)
The Baeyer-Villiger monooxygenases (BVMOs) are a family of bacterial flavoproteins that catalyze the synthetically useful Baeyer-Villiger oxidation reaction. This involves the conversion of ketones into esters or cyclic ketones into lactones by introducing an oxygen atom adjacent to the carbonyl

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