Chemical Properties Usage Preparation Category Toxicity grade Acute toxicity Flammability hazard characteristics Storage Fire extinguishing agents
ChemicalBook > CAS DataBase List > 2,6-Lutidine

2,6-Lutidine

Chemical Properties Usage Preparation Category Toxicity grade Acute toxicity Flammability hazard characteristics Storage Fire extinguishing agents
Product Name
2,6-Lutidine
CAS No.
108-48-5
Chemical Name
2,6-Lutidine
Synonyms
2,6-DIMETHYLPYRIDINE;2,6-Lutdeine;2,6-Lutidene;2,6-Dimethypyridine;utidine;2,6-Lutidine 2,6-Dimethylpyridine;26L;NSC 2155;FEMA 3540;2,6-LUTIDINE
CBNumber
CB6852755
Molecular Formula
C7H9N
Formula Weight
107.15
MOL File
108-48-5.mol
More
Less

2,6-Lutidine Property

Melting point:
-6 °C (lit.)
Boiling point:
143-145 °C (lit.)
Density 
0.92 g/mL at 25 °C (lit.)
vapor pressure 
5.5 hPa (20 °C)
FEMA 
3540 | 2,6-DIMETHYLPYRIDINE
refractive index 
n20/D 1.497(lit.)
Flash point:
92 °F
storage temp. 
−20°C
solubility 
Chloroform (Soluble), Methanol (Slightly)
pka
6.65(at 25℃)
form 
Liquid
color 
Clear
Odor
at 1.00 % in dipropylene glycol. nutty amine woody bready cocoa oily
Odor Type
nutty
Water Solubility 
40 g/100 mL (20 ºC)
Sensitive 
Hygroscopic
JECFA Number
1317
Merck 
14,5616
BRN 
105690
Dielectric constant
7.3300000000000001
Stability:
Stable. Flammable. Incompatible with strong oxidizing agents, acid chlorides, acids, chloroformates. Protect from moisture.
LogP
0.12 at 25℃
CAS DataBase Reference
108-48-5(CAS DataBase Reference)
NIST Chemistry Reference
Pyridine, 2,6-dimethyl-(108-48-5)
EPA Substance Registry System
2,6-Dimethylpyridine (108-48-5)
More
Less

Safety

Hazard Codes 
Xn,F,Xi
Risk Statements 
10-22-36/37/38-20/21/22
Safety Statements 
26-36/37-16-36-36/37/39
RIDADR 
UN 1993 3/PG 3
WGK Germany 
3
RTECS 
OK9700000
8
Hazard Note 
Irritant/Flammable
TSCA 
Yes
HazardClass 
3
PackingGroup 
III
HS Code 
29333999
Hazardous Substances Data
108-48-5(Hazardous Substances Data)
Toxicity
LD50 orally in Rabbit: 400 mg/kg LD50 dermal Rabbit > 1000 mg/kg
More
Less

Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H226Flammable liquid and vapour

H302Harmful if swallowed

H315Causes skin irritation

H319Causes serious eye irritation

Precautionary statements

P210Keep away from heat/sparks/open flames/hot surfaces. — No smoking.

P302+P352IF ON SKIN: wash with plenty of soap and water.

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

More
Less

N-Bromosuccinimide Price

Sigma-Aldrich
Product number
W354007
Product name
2,6-Dimethylpyridine
Purity
≥99%
Packaging
1kg
Price
$204
Updated
2024/03/01
Sigma-Aldrich
Product number
W354007
Product name
2,6-Dimethylpyridine
Purity
≥99%
Packaging
5kg
Price
$1080
Updated
2024/03/01
Sigma-Aldrich
Product number
W354007
Product name
2,6-Dimethylpyridine
Purity
≥99%
Packaging
10Kg
Price
$1990
Updated
2024/03/01
Sigma-Aldrich
Product number
L3900
Product name
2,6-Lutidine
Purity
ReagentPlus?, 98%
Packaging
100mL
Price
$46.3
Updated
2024/03/01
Sigma-Aldrich
Product number
L3900
Product name
2,6-Lutidine
Purity
ReagentPlus?, 98%
Packaging
500mL
Price
$116
Updated
2024/03/01
More
Less

2,6-Lutidine Chemical Properties,Usage,Production

Chemical Properties

Colorless oily liquid, melting point-5.8℃, boiling point 144℃(139-141℃,145.6-145.8℃), density 0.9252(20/4℃), refractive index 1.4977, flash point 33℃, soluble in dimethyl formamide, tetrahydrofuran, cold water, hot water, ethanol and ether, with mixed odor of Pyridine and mint.

Usage

2,6-Lutidine is widely used in organic synthesis as a raw material and solvent. In Pharmaceutical industry, it can be used for the production of antiatherosclerotic pyridinolcarbamate. It can also be used for the production of Cortisone acetate, hydrocortisone, niacin, lobeline and stilbazium iodide which is an anthelmintic and effective for the worm, fasciolopsis buski, whipworm, pinworm and so on. In addition, 2,6-Lutidine can be used as an auxiliaries for Pesticides, dyes, dyeing and printing and used as resin and rubber accelerator,  intermediate of hot oil stabilizer.  It  can be oxidized to produce Dimethyl pyridine acid, which can be used as the stabilizer for hydrogen peroxide and acetic acid and used to synthesize lobelidine. 2,6-Lutidine is used as various kinds of nutty essence and cocoa, coffee, meat, bread and vegetable typed essence. It is also used to synthesize drugs for the treatment and first-aid of hypertension.

Preparation

2,6-Lutidine is obtained through the separation of β-methylpyridine which is a recycled product of coal coking byproduct.

Category

flammable liquid

Toxicity grade

high toxic

Acute toxicity

oral – rat LD50: 400mg/kg

Flammability hazard characteristics

flammable in case of fire, high temperature and oxidant, releasing toxic nitrogen oxides in case of heat.

Storage

Ventilated and dry warehouse with low temperature, separated from acids.

Fire extinguishing agents

Dry powder, dry sand, carbon dioxide, foam.

Chemical Properties

Colorless to yellow liquid

Chemical Properties

2,6-Dimethylpyridine has a powerful and diffusive minty-tarry odor. It has also been described to have the odor of pyridine and peppermint

Occurrence

Reported found in bread, tea, peppermint oil, cheeses, chicken, beef, pork, beer, sherry, whiskies, cocoa, coffee, tea, oatmeal, rice bran, buckwheat and malt.

Uses

2,6-Lutidine is used as a solvent in organic synthesis and as a sterically hindered mild base. It is also used as a vulcanization accelerator for dyes, resins and rubber. It also acts as a food additive.

Uses

Isolated from the basic fraction of coal tar. A semi-volatile compound in tobacco.

Definition

ChEBI: A member of the class of methylpyridines that is pyridine carrying methyl substituents at positions 2 and 6.

Taste threshold values

Taste characteristics at 20 ppm: nutty, coffee, cocoa, musty, bready and meaty

Synthesis Reference(s)

Organic Syntheses, Coll. Vol. 2, p. 214, 1943
Tetrahedron Letters, 17, p. 383, 1976 DOI: 10.1016/S0040-4039(00)93738-9

General Description

A colorless liquid with a peppermint odor. Flash point 92°F. Less dense than water. Vapors heavier than air. Produces toxic oxides of nitrogen during combustion. Used to make other chemicals.

Air & Water Reactions

Highly flammable. Soluble in water.

Reactivity Profile

2,6-Lutidine neutralizes acids in exothermic reactions to form salts plus water. May be incompatible with isocyanates, halogenated organics, peroxides, phenols (acidic), epoxides, anhydrides, and acid halides. Flammable gaseous hydrogen may be generated in combination with strong reducing agents, such as hydrides.

Health Hazard

Inhalation or contact with material may irritate or burn skin and eyes. Fire may produce irritating, corrosive and/or toxic gases. Vapors may cause dizziness or suffocation. Runoff from fire control or dilution water may cause pollution.

Flammability and Explosibility

Flammable

Synthesis

Synthesis from ethyl acetoacetate, formaldehyde and ammonia; isolated from basic fraction of coal tar

Purification Methods

Likely contaminants include 3-and 4-picoline (similar boiling points). However, they are removed by using BF3, with which they react preferentially, by adding 4mL of BF3 to 100mL of dry fractionally distilled 2,6-lutidine and redistilling. Distillation of commercial material from AlCl3 (14g per 100mL) can also be used to remove picolines (and water). Alternatively, lutidine (100mL) can be refluxed with ethyl benzenesulfonate (20g) or ethyl p-toluenesulfonate (20g) for 1hour, then the upper layer is cooled, separated and distilled. The distillate is refluxed with BaO or CaH2, then fractionally distilled through a glass helices-packed column. 2,6-Lutidine can be dried with KOH or sodium or by refluxing with (and distilling from) BaO, prior to distillation. For purification via its picrate, 2,6-lutidine, dissolved in absolute EtOH, is treated with an excess of warm ethanolic picric acid. The precipitate is filtered off, recrystallised from acetone (to give m 163-164.5o (166-167o), and partitioned between ammonia and CHCl3/diethyl ether. The organic layer, after washing with dilute aqueous KOH, is dried with Na2SO4 and fractionally distilled. [Warnhoff J Org Chem 27 4587 1962.] Alternatively, 2,6-lutidine can be purified via its urea complex, as described under 2,3-lutidine. Other purification procedures include azeotropic distillation with phenol [Coulson et al. J Appl Chem (London) 2 71 1952], fractional crystallisation by partial freezing, and vapour-phase chromatography using a 180-cm column of polyethylene glycol-400 (Shell, 5%) on Embacel (May and Baker) at 100o, with argon as carrier gas [Bamford & Block J Chem Soc 4989 1961]. The hydrochloride has m 235-237o, 239o (from EtOH). [Beilstein 20 II 160, 20 III/IV 2776, 20/6 V 32.]

More
Less

2,6-Lutidine Suppliers

Molekula Ltd
Tel
--
Fax
--
Email
info@molekula.com
Country
United Kingdom
ProdList
4060
Advantage
50
Melrob Ltd (part of Nordmann)
Tel
--
Fax
--
Email
nquiries@melrob.com
Country
United Kingdom
ProdList
3065
Advantage
58
Molekula Limited
Tel
--
Fax
--
Email
o@molekula.com
Country
United Kingdom
ProdList
6127
Advantage
58
Cenik Chemicals
Tel
--
Fax
--
Email
lo@cenikchemicals.com
Country
United Kingdom
ProdList
1681
Advantage
58
Apollo Scientific Ltd
Tel
--
Fax
--
Email
ales@apo
Country
United Kingdom
ProdList
4521
Advantage
58
Alcan Chemicals Europe
Tel
--
Fax
--
Country
United Kingdom
ProdList
99
Advantage
58
Hawks Chemical Company Limited
Tel
--
Fax
--
Email
pete@hawks-chem.com
Country
United Kingdom
ProdList
600
Advantage
58
OQEMA (Formerly Lansdowne Chemicals Plc)
Tel
--
Fax
--
Email
info@oqema.co.uk
Country
United Kingdom
ProdList
182
Advantage
58
CMS Chemicals Limited
Tel
--
Fax
--
Email
cms.marketing@cms-chemicals.com
Country
United Kingdom
ProdList
3708
Advantage
60
Manchester Organics
Tel
--
Fax
--
Email
info@manchesterorganics.com
Country
United Kingdom
ProdList
6834
Advantage
67
Biosynth Carbosynth
Tel
--
Fax
--
Email
ales@carbosynth.com
Country
United Kingdom
ProdList
2598
Advantage
58
Whyte Chemicals
Tel
--
Fax
--
Email
sales@whytechemicals.co.uk
Country
United Kingdom
ProdList
3748
Advantage
50
Apollo Scientific Ltd.
Tel
--
Fax
--
Email
sales@apolloscientific.co.uk
Country
United Kingdom
ProdList
6084
Advantage
88
CARBONE SCIENTIFIC CO.,LTD
Tel
--
Fax
--
Email
sales@carbonesci.com
Country
United Kingdom
ProdList
6666
Advantage
30
Carbosynth Limited
Tel
--
Fax
--
Email
sales@carbosynth.com
Country
United Kingdom
ProdList
6581
Advantage
61
Leancare Ltd.
Tel
--
Fax
--
Email
enquiry@leancare.co.uk
Country
United Kingdom
ProdList
6446
Advantage
42
Lansdowne Chemicals Plc
Tel
--
Fax
--
Email
robert.moss@lansdownechemicals.com
Country
United Kingdom
ProdList
576
Advantage
51
MOLEKULA Ltd.
Tel
--
Fax
--
Email
kevinbanks@molekula.com
Country
United Kingdom
ProdList
6140
Advantage
66
ETA SCIENTIFIC Co.,Ltd
Tel
--
Fax
--
Email
sales@etascientific.com
Country
United Kingdom
ProdList
6090
Advantage
34
VWR International
Tel
--
Fax
--
Email
solutions@vwr.com
Country
United Kingdom
ProdList
6548
Advantage
82
Vertellus Specialties UK Ltd. (formerly Seal Sands Chemicals Ltd.)
Tel
--
Fax
--
Email
CSRs@vertellus.com
Country
United Kingdom
ProdList
198
Advantage
73
Eurolabs Limited
Tel
--
Fax
--
Country
United Kingdom
ProdList
6309
Advantage
46
MDA Chemicals Ltd.
Tel
--
Fax
--
Email
sheila@mda-chem.co.uk
Country
United Kingdom
ProdList
1961
Advantage
30
More
Less

View Lastest Price from 2,6-Lutidine manufacturers

Qingdao RENAS Polymer Material Co., Ltd.
Product
2,6-Lutidine 108-48-5
Price
US $0.00/kg
Min. Order
20kg
Purity
99%
Supply Ability
20 tons
Release date
2024-09-12
Hebei Weibang Biotechnology Co., Ltd
Product
2,6-Lutidine 108-48-5
Price
US $10.00/KG
Min. Order
1KG
Purity
99%
Supply Ability
10 mt
Release date
2021-08-05
Hebei Mojin Biotechnology Co., Ltd
Product
2,6-Lutidine 108-48-5
Price
US $0.00/KG
Min. Order
1KG
Purity
99%
Supply Ability
50000KG/month
Release date
2023-06-27

108-48-5, 2,6-LutidineRelated Search:


  • FEMA 3540
  • FEMA NUMBER 3540
  • DIMETHYLPYRIDINE(2,6-)
  • 2,6-Lutidine 2,6-Dimethylpyridine
  • 26L
  • 2,6-DIMETHYLPYRIDINE
  • 2,6-LUTIDINE
  • 2 6-DIMETHYLPYRIDINE 99+%
  • 2,6-LUTIDINE, REDISTILLED, 99+%
  • 2 6-LUTIDINE REAGENTPLUS(TM) 99%
  • 2,6-LUTIDINE, STANDARD FOR GC
  • 2,6-LUTIDINE 99%
  • 2,6-DIMETHYLPYRIDINE-D9 98%
  • 2,6-Lutidine, 98+%
  • 2,6-Lutidine, spectro grade, 99%
  • 2,6-Lutdeine
  • 2,6-Dimethylpyridine 98+%
  • 2,6-Lutidine, redistilled
  • 2,6-Dimethylpyridine, 2,6-Lutidine
  • 2,6-Lutidine ,99%
  • 2,6-Lutidine,99%,spectro grade
  • 2,6-Dimethylpyridine,2,6-Dimethylpyridine, 2,6-Lutidine
  • 2,6-dimethyl-pyridin
  • 2,6-Dimethypyridine
  • 2,6-Lutidene
  • alpha,alpha’-dimethylpyridine
  • alpha,alpha’-lutidin
  • alpha,alpha’-lutidine
  • alpha,alpha'-Dimethylpyridine
  • alpha,alpha'-Lutidin
  • alpha,alpha'-Lutidine
  • Pyridine,2,6-dimethyl-
  • 2,6-Lutidine, 99% 250ML
  • NSC 2155
  • 2,6-Lutidine, 99%, purified by redistillation, AcroSeal
  • 2,6-DIMETHYLPYRIDINE FOR SYNTHESIS
  • 2,6-Lutidine, redistillation
  • 2,6-Lutidine purified by redistillation, >=99%
  • 2,6-Lutidine ReagentPlus(R), 98%
  • 2,6-dimethyl-pyridin 2,6-Dimethypyridine 2,6-Lutidene
  • 2,6-Lutidine, 99%, redistillation
  • utidine
  • 2,6-Lutidine/2,6-Dimethypyridine
  • 2,6-Dimethylpyridine(or2,6-Lutidine)
  • 2,6-Lutidine&gt
  • Bayer resin -181
  • *Trolamine Impurity 2 (Trolamine EP Impurity B)
  • 2, 6-Lutidine 99% For Synthesis
  • 2,6-Lutidine1G
  • 108-48-5
  • 488-96-8
  • 2,6-LUTIDINE
  • CH32C5H3N
  • Fatty Acids
  • Heterocyclic Building Blocks
  • Chromatography
  • Esters
  • Natural Compounds