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Merck
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Documentos

04991

Supelco

2,6-Lutidina

analytical standard

Sinônimo(s):

2,6-Dimetilpiridina

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About This Item

Fórmula empírica (Notação de Hill):
C7H9N
Número CAS:
108-48-5
Peso molecular:
107.15
Beilstein:
105690
Número CE:
203-587-3
Número MDL:
MFCD00006345
Código UNSPSC:
85151701
ID de substância PubChem:
329747999
NACRES:
NA.24

grau

analytical standard

Nível de qualidade

100

Ensaio

≥99.7% (GC)

prazo de validade

limited shelf life, expiry date on the label

técnica(s)

HPLC: suitable
gas chromatography (GC): suitable

índice de refração

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

pb

143-145 °C (lit.)

pf

−6 °C (lit.)

densidade

0.92 g/mL at 25 °C (lit.)

aplicação(ões)

cleaning products
cosmetics
flavors and fragrances
food and beverages
personal care

formato

neat

cadeia de caracteres SMILES

Cc1cccc(C)n1

InChI

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

chave InChI

OISVCGZHLKNMSJ-UHFFFAOYSA-N

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Categorias relacionadas

Pictogramas

FlameExclamation mark
GHS02,GHS07

Palavra indicadora

Warning

Frases de perigo

H226,H302,H315,H319

Classificações de perigo

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

Código de classe de armazenamento

3 - Flammable liquids

Classe de risco de água (WGK)

WGK 3

Ponto de fulgor (°F)

91.4 °F

Ponto de fulgor (°C)

33 °C

Equipamento de proteção individual

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

Choose from one of the most recent versions:

Certificados de análise (COA)

Lot/Batch Number
BCCK5325
BCCF7883
BCCB7273
BCBV0328
BCBS1431V

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Sigma-Aldrich

32222

Diclorometano

tert-Butyldimethylsilyl trifluoromethanesulfonate reagent grade, 98%

Sigma-Aldrich

226149

tert-Butyldimethylsilyl trifluoromethanesulfonate

2,6-Di-tert-butylpyridine ≥97%

Sigma-Aldrich

219584

2,6-Di-tert-butylpyridine

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Sigma-Aldrich

41640

Dimetilsulfóxido

2,4,6-Trimethylpyridine puriss. p.a., 99% (GC)

Sigma-Aldrich

27690

2,4,6-Trimethylpyridine

Hexamethylenetetramine ACS reagent, ≥99.0%

Sigma-Aldrich

398160

Hexamethylenetetramine

Anidrido trifluorometanossulfônico 99%

Sigma-Aldrich

176176

Anidrido trifluorometanossulfônico

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
Jun Gao et al.
Journal of hazardous materials, 130(1-2), 141-147 (2005-10-26)
The homogeneous catalytic N-oxidation of two picolines and two lutidines by hydrogen peroxide has been studied calorimetrically using a heat flow and power compensation SIMULAR reaction calorimeter. The objective of this work was to extend a previously developed kinetic model
Ikuo Nakanishi et al.
Organic & biomolecular chemistry, 3(4), 626-629 (2005-02-11)
The scavenging reaction of 2,2-diphenyl-1-picrylhydrazyl radical (DPPH.) or galvinoxyl radical (GO.) by a vitamin E model, 2,2,5,7,8-pentamethylchroman-6-ol (1H), was significantly accelerated by the presence of Mg(ClO4)2 in de-aerated methanol (MeOH). Such an acceleration indicates that the radical-scavenging reaction of 1H
S R Agapova et al.
Molekuliarnaia genetika, mikrobiologiia i virusologiia, (5-6)(5-6), 10-13 (1992-05-01)
Arthrobacter crysallopoietes strain KM-4 degrading 2,6-dimethylpyridine and strain KM-4a degrading both 2,6-dimethylpyridine and pyridine, Arthrobacter sp. KM-4b degrading 2,4-dimethylpyridine were isolated from soil. Arthrobacter crystallopoietes KM-4 and Arthrobacter sp. KM-4b contain 100 Md plasmids pBS320 and pBS323. Arthrobacter crystallopietes KM-4a
Asymmetric fluorination of alpha-aryl acetic acid derivatives with the catalytic system NiCl2-Binap/R3SiOTf/2,6-lutidine.
Toshiaki Suzuki et al.
Angewandte Chemie (International ed. in English), 46(28), 5435-5439 (2007-06-15)
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