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Merck

04991

Supelco

2,6-二甲基吡啶

analytical standard

别名:

2,6-卢剔啶

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About This Item

经验公式(希尔记法):
C7H9N
CAS号:
分子量:
107.15
Beilstein:
105690
EC號碼:
MDL號碼:
分類程式碼代碼:
85151701
PubChem物質ID:
NACRES:
NA.24

等級

analytical standard

品質等級

化驗

≥99.7% (GC)

儲存期限

limited shelf life, expiry date on the label

技術

HPLC: suitable
gas chromatography (GC): suitable

折射率

n20/D 1.497 (lit.)
n20/D 1.499

bp

143-145 °C (lit.)

mp

−6 °C (lit.)

密度

0.92 g/mL at 25 °C (lit.)

應用

cleaning products
cosmetics
flavors and fragrances
food and beverages
personal care

形式

neat

SMILES 字串

Cc1cccc(C)n1

InChI

1S/C7H9N/c1-6-4-3-5-7(2)8-6/h3-5H,1-2H3

InChI 密鑰

OISVCGZHLKNMSJ-UHFFFAOYSA-N

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象形圖

FlameExclamation mark

訊號詞

Warning

危險分類

Acute Tox. 4 Oral - Eye Irrit. 2 - Flam. Liq. 3 - Skin Irrit. 2

儲存類別代碼

3 - Flammable liquids

水污染物質分類(WGK)

WGK 3

閃點(°F)

89.6 °F

閃點(°C)

32 °C

個人防護裝備

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


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Wensheng Yu et al.
Organic letters, 6(19), 3217-3219 (2004-09-10)
[reaction: see text] Oxidative cleavage of olefins by OsO(4)-NaIO(4) sometimes suffers from low yields due to the formation of side products. It is found that the addition of 2,6-lutidine can suppress the side reactions and dramatically improve the yield of
Cyrille Costentin et al.
Journal of the American Chemical Society, 132(29), 10142-10147 (2010-07-06)
The effect of base pairing by cytosine on the electrochemical oxidation of guanine is examined by means of cyclic voltammetry on carefully purified reactants in a solvent, CHCl(3), which strongly favors the formation of an H-bonded pair. The thermodynamics and
Kathryn A White et al.
Journal of colloid and interface science, 359(1), 126-135 (2011-04-22)
Using a system of modified silica particles and mixtures of water and 2,6-lutidine to form particle-stabilized emulsions, we show that subtle alterations to the hydration of the particle surface can cause major shifts in emulsion structure. We use fluorescence confocal
Qingnan Liu et al.
The journal of physical chemistry. A, 113(16), 4387-4396 (2009-03-24)
Collision rates and energy transfer distributions are reported for HOD with highly vibrationally excited 2-methylpyridine (2-picoline, E = 38 310 cm(-1)) and 2,6-dimethylpyridine (2,6-lutidine, E = 38 700 cm(-1)). High resolution transient IR absorption is used measured to complete product
Elena Arceo et al.
Nature chemistry, 5(9), 750-756 (2013-08-24)
Asymmetric catalytic variants of sunlight-driven photochemical processes hold extraordinary potential for the sustainable preparation of chiral molecules. However, the involvement of short-lived electronically excited states inherent to any photochemical reaction makes it challenging for a chiral catalyst to dictate the

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