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Merck

48292

Supelco

苯乙酮 溶液

certified reference material, 2000 μg/mL in methylene chloride

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About This Item

经验公式(希尔记法):
C8H8O
CAS号:
分子量:
120.15
EC號碼:
分類程式碼代碼:
12000000

等級

certified reference material

CofA

current certificate can be downloaded

包裝

ampule of 1 mL

濃度

2000 μg/mL in methylene chloride

技術

HPLC: suitable
gas chromatography (GC): suitable

應用

environmental

格式

single component solution

儲存溫度

2-30°C

InChI

1S/C8H8O/c1-7(9)8-5-3-2-4-6-8/h2-6H,1H3

InChI 密鑰

KWOLFJPFCHCOCG-UHFFFAOYSA-N

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應用

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

象形圖

Health hazardExclamation mark

訊號詞

Warning

危險分類

Carc. 2 - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

標靶器官

Central nervous system

儲存類別代碼

6.1D - Non-combustible acute toxic Cat.3 / toxic hazardous materials or hazardous materials causing chronic effects

水污染物質分類(WGK)

WGK 2

閃點(°F)

Not applicable

閃點(°C)

Not applicable


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分析证书(COA)

Lot/Batch Number

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Dejan Vražič et al.
Molecules (Basel, Switzerland), 18(1), 74-96 (2013-01-25)
The Brønsted-acidic ionic liquid 1-methyl-3-(4-sulfobutyl)imidazolium triflate [BMIM(SO(3)H)][OTf] was demonstrated to act efficiently as solvent and catalyst for the halogenation of activated organic compounds with N-halosuccinimides (NXS) under mild conditions with short reaction times. Methyl aryl ketones were converted into α-halo
Raphaël F Guignard et al.
Chemical communications (Cambridge, England), 47(44), 12185-12187 (2011-10-15)
A new concise route to Polycyclic Aromatic Hydrocarbons (PAHs) through radical addition and cyclisation of xanthates is described.
V Selvarani et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 91, 329-337 (2012-03-14)
Four tetradentate (N(2)O(2)) and tridentate (NO(2)) Schiff base compounds (L1-L4) with propargyl moiety were prepared by the condensation of 1-[2-hydroxy-4-(prop-2-yn-1-yloxy)phenyl]ethanone with various aliphatic amines. The newly synthesized compounds (L1-L4) were characterized on the basis of the results of elemental analysis
Eric R Bittner et al.
The Journal of chemical physics, 137(22), 22A551-22A551 (2012-12-20)
The standard model for molecular recognition of an odorant is that receptor sites discriminate by molecular geometry as evidenced that two chiral molecules may smell very differently. However, recent studies of isotopically labeled olfactants indicate that there may be a
Yuka Inatomi et al.
Journal of natural medicines, 67(2), 359-368 (2012-08-01)
New glycosides of seven acetophenone derivatives (1-7) and two phenylpropanoids (8, 9), named juniperosides III-XI, have been isolated from the MeOH extract of the leaves and stems of Juniperus occidentalis Hook. (Cupressaceae), together with eleven other known compounds. The structures

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