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L3609

2,4-二甲基吡啶

Name: 2,4-二甲基吡啶
Brand: ALDRICH

99%

别名:

2,4-卢剔啶

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关于此项目

经验公式（希尔记法）:

C₇H₉N

化学文摘社编号:

108-47-4

分子量:

107.15

UNSPSC Code:

12352100

NACRES:

NA.22

PubChem Substance ID:

24896348

EC Number:

203-586-8

Beilstein/REAXYS Number:

1506

MDL number:

MFCD00006337

Assay:

99%

Form:

liquid

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属性

Quality Level

100

assay

99%

form

liquid

refractive index

n20/D 1.499 (lit.)

bp

159 °C (lit.)

mp

−60 °C (lit.)

density

0.927 g/mL at 25 °C (lit.)

SMILES string

Cc1ccnc(C)c1

InChI

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

InChI key

JYYNAJVZFGKDEQ-UHFFFAOYSA-N

说明

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pictograms

GHS02,GHS06

signalword

Danger

hcodes

H226,H301 + H311 + H331,H315,H319,H335

pcodes

P210 - P280 - P301 + P310 - P303 + P361 + P353 - P304 + P340 + P311 - P305 + P351 + P338

Hazard Classifications

Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Eye Irrit. 2 - Flam. Liq. 3 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

存储类别

3 - Flammable liquids

wgk

WGK 3

flash_point_f

116.6 °F - closed cup

flash_point_c

47 °C - closed cup

ppe

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

法规信息

危险化学品

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历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Chemical standards in ion mobility spectrometry.

Roberto Fernández-Maestre et al.

The Analyst, 135(6), 1433-1442 (2010-04-07)

In ion mobility spectrometry (IMS), reduced mobility values (K(0)) are used as a qualitative measure of gas phase ions, and are reported in the literature as absolute values. Unfortunately, these values do not always match with those collected in the

Factors dictating the nuclearity/aggregation and acetate coordination modes of lutidine-coordinated zinc(II) acetate complexes.

Umesh Kumar et al.

Inorganic chemistry, 49(1), 62-72 (2009-12-05)

The reactions of Zn(OAc)(2).2H(2)O with various positional isomers of lutidine were explored with a view to understand the factors responsible for the nuclearity/aggregation and acetate coordination modes of the products. The reactions of Zn(OAc)(2).2H(2)O with 3,5-lutidine, 2,3-lutidine, 2,4-lutidine, and 3,4-lutidine

Synthesis and anti-inflammatory activity of polyazaheterocyclic derivatives of 6-amino-2,4-lutidine and their precursors.

J M Robert et al.

Arzneimittel-Forschung, 47(5), 635-642 (1997-05-01)

Derivatives of N-(4,6-pyridin-2-yl)arylcarboxamides resulting from the integration of the amidic function into 4H-1,2,4-triazole, triazol-3(2H)-one and 1H-tetrazole rings were evaluated as potential anti-inflammatory compounds. The level of activity decreased as compared to carboxamides, nevertheless their precursors and notably the corresponding amidrazones

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全球贸易项目编号

货号	GTIN
L3609-100ML	04061833951163
L3609-500ML	04061833951187
L3609-5ML	04061837669545