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3-??????

3-??????
3-?????? ??? ???
?? ??:
350-03-8
???:
3-??????
???(??):
3-??????
???:
3-Acetylpyridine
???(??):
FEMA 3424;3-Acetylpiridine;methylpyridylketone;1-(3-PYRIDINYL)ETHANONE;1-(3-pyridenyl)ethanone;Ethanone,1-(3-pyridinyl)-;NSC 761;Imatinib-int A;3-ActylPyridine;3-ACETOPYRIDINE
CBNumber:
CB9286704
???:
C7H7NO
??? ??:
121.14
MOL ??:
350-03-8.mol
MSDS ??:
SDS

3-?????? ??

???
11-13 °C (lit.)
?? ?
220 °C (lit.)
??
1.102 g/mL at 25 °C (lit.)
???
0.3Pa at 20℃
FEMA
3424 | 3-ACETYLPYRIDINE
???
n20/D 1.534(lit.)
???
302 °F
?? ??
Inert atmosphere,Room Temperature
???
?????(?? ???), ???(?? ???)
?? ?? (pKa)
pK1: 3.256(+1) (25°C)
??? ??
??
??
??~???? ???
Specific Gravity
1.102
??????(pH)
6.5-7.5 (H2O, 20℃)
??
????? ??? ? 1.00%. ???? ??? ??? ?? ??? ?? ??
?? ??
???
???? ??
synthetic
???
??? ?? ???
Merck
14,6116
JECFA Number
1316
BRN
107751
Henry's Law Constant
4.6×102 mol/(m3Pa) at 25℃, Abraham et al. (1994)
?? ??
?? ? ?
InChI
1S/C7H7NO/c1-6(9)7-3-2-4-8-5-7/h2-5H,1H3
InChIKey
WEGYGNROSJDEIW-UHFFFAOYSA-N
SMILES
CC(=O)c1cccnc1
LogP
0.34 at 13℃
CAS ??????
350-03-8(CAS DataBase Reference)
NIST
Ethanone, 1-(3-pyridinyl)-(350-03-8)
EPA
Ethanone, 1-(3-pyridinyl)- (350-03-8)
??
  • ?? ? ?? ??
  • ?? ? ???? ?? (GHS)
??? ?? T,Xi,Xn
?? ???? ?? 25-36/38-36/37/38-20/21/22
????? 45-37/39-28A-26-36
????(UN No.) UN 2810 6.1/PG 3
WGK ?? 3
RTECS ?? OB5425000
F ?????? 8-10
?? ?? ?? Irritant
TSCA TSCA listed
?? ?? 6.1
???? II
HS ?? 29333999
???? ??? 6.1C - Combustible acute toxic Cat.3
toxic compounds or compounds which causing chronic effects
Hazard Classifications Acute Tox. 3 Oral
Skin Irrit. 2
?? LD50 orl-rat: 46 mg/kg JACTDZ 1,681,92
????(GHS): Skull and Crossbones (GHS06)
?? ?: Danger
??·?? ??:
?? ??·?? ?? ?? ?? ?? ?? ? ?? ?? P- ??
H301 ??? ??? ?? ?? ?? - ?? ?? 3 ?? P264, P270, P301+P310, P321, P330,P405, P501
H315 ??? ??? ??? ????? ?? ????? ?? 2 ?? P264, P280, P302+P352, P321,P332+P313, P362
??????:
P264 ?? ??? ?? ??? ????.
P264 ?? ??? ?? ??? ????.
P270 ? ??? ??? ??? ???, ???? ???? ???.
P280 ????/???/???/?????? ?????.
P301+P310 ???? ?? ????(??)? ??? ????.
P302+P352 ??? ??? ??? ?? ????.
P332+P313 ?? ??? ??? ???? ??· ??? ????.
NFPA 704
0
3 0

3-?????? MSDS


Methyl 3-pyridyl ketone

3-?????? C??? ??, ??, ??

??

Reported found in roasted filberts, beer, brandy, coffee, malt and wheaten bread.

??

3-Acetylpyridine used as an intermediate for the synthesis of risedronate sodium, inhibitor of bone resorption. It is also used in perfumery.

?? ??

Produced from Ethyl nicotinate and Ethyl acetoacetate, in principle by hydrolysis of Aceto acetylpyridine.

?? ??

Dry distillation of calcium nicotinate with calcium acetate.

??

It is a nicotinic acidantagonist.

Safety Profile

Poison by ingestion. Moderately toxic by intraperitoneal routeMutation data reported. A flammable liquid. When heated to decomposition emits toxic fumes of NOx,. See also KETONES

Synthesis

A mixture of 22 g/h of methyl nicotinate, 57 g/h of acetic acid and 20 g/h of water was evaporated in an evaporator and passed, together with 10 l/h of nitrogen, at 400° C., over 100 ml of catalyst, which contained 2% by weight of sodium oxide, the remainder being anatase. The catalyst was prepared by impregnating 980 g of TiO2 carrier I with a solution which contained 20 g of Na2O (as aqueous NaOH). The reaction gases were then cooled and were collected in a receiver. From the discharged two-phase mixture, the organic phase was analyzed by gas chromatography. The selectivity with respect to 3-acetylpyridine was 60%.

Purification Methods

It is purified by dissolving in HCl, extracting with Et2O to remove the possible impurity of nicotinic acid, basified with NaOH and extracted with Et2O. The dried extract is filtered, evaporated and the residual oil is distilled. If the NMR spectrum indicates further impurities, then convert it to the phenylhydrazone (m 137o, yellow needles from EtOH). This is hydrolysed with HCl [Engler & Kiby Chem Ber 22 597 1889], the phenylhydrazine HCl is removed by filtration, NaNO2 is added, the solution is basified with aqueous NaOH and extracted with Et2O as before and distilled at atmospheric pressure to give 3-acetylpyridine as a colourless oil. Purification can also be achieved by shaking with 50% aqueous KOH, extracting with Et2O, drying the extract and distilling it at atmospheric pressure or in vacuo. [Kloetzel & Chubb J Am Chem Soc 79 4226 1957.] The hydrochloride has m 180-181o (from MeOH/EtOH), the picrate has m 133.8-134.8o (from H2O), and the phenylhydrazone has m 137o (129-130o)(needles, from EtOH) [Webb & Webb J Am Chem Soc 71 2285 1949]. The ketoxime has m 112o (from EtOH or *C6H6). [Strong & McElvain J Am Chem Soc 55 816 1933, Kolloff & Hunter J Am Chem Soc 63 490 1941, Beilstein 21/7 V 394.]

3-?????? ?? ?? ? ???

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?? ??


3-?????? ?? ??

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