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Methyl heptenone（ PG）Basic informationes

Product nomen:	Methyl heptenone（PG）
Synonyma:	2-methyl-6-oxo-2-heptene;2-methylhept-2-en-6-one; methyI-5-hepten-2-one; 6 methyl-5-hepten-2-on; 97.50%
CAS;	110-93-0
MF:	C8H14O
MW:	126.2
EINECS:	203-816-7
Categoria:	Alphabetical Listings, Naturalis ProductsFlavors Certified et odores, sapores et odores, M-N; C7 ad C8, Carbonyl Composita, Ketones
Mol fasciculi:	110-93-0.mol

Methyl heptenone（ PG）Chemical Properties

punctum liquescens	-67.1 °C
fervens	73 °C18 mm Hg (lit.)
density	0.855 g/mL at 25 °C(lit.)
FEMA	2707 \| 6-METHYL-5-HEPTEN-2-ONE
refractivus index	n20/D 1.439(lit.)
Fp	123 °F
repono temp.	Flammabiles area
solubility	Solutum methanolum et chloroform.
forma	tersus
Gravitas Imprimis	0.855
PH	6.6 (3g/l, H2O, 25℃)
explosive modum	1.1-7.3%(V)
Aqua Solubility	insolubilis
JECFA Number	1120
BRN	1741705
CAS Reference	110-93-0 (CAS Reference)
NIST Chemia Reference	5-Hepten-2-one, 6-methyl-(110-93-0)
EPA Substantia Registry System	6-Methyl-5-hepten-2-one (110-93-0)

Methyl heptenone（PG）Safety Information

Periculum Denunciationes	10-36/37/38
Salus Denunciationes	16-24/25
RIDADR	UN 1224 3/PG 3
WGK Germania	1
RTECS	MJ9700000
TSCA	Ita
HazardClass	3
PackingGroup	III
HS Code	29141990

Methyl heptenone PG, Synthesis et Synthesis

Descriptio	methyl heptenone（PG）has fortis; pinguis, viridis, odoris citri, et saporis amarissimi simile piri. Praeparari potest ex oleo lemongrass vel ex citrali per refluxus 12 . horas in solutione aquea K2C 03 continens, et destillationem subsequentem et fractio vacuum; ex acetoacetic ester et methylbuten-3-ol-2 cum aluminium alcoholatum in reactione Carroll sequitur pyrolysis ester.
Chemical Properties	Methyl heptenone（PG）e fortis habet; pinguis, viridis, citri similis, odoris et saporis amarissimi simile piri.
Chemical Properties	SERENUS LEVITER CLAVUS LIQUIDUS
Chemical Properties	Methyl heptenone PG）is magni momenti medium in synthesi terpenoidum. Odorem proprietates non sunt gravem. Fit in natura ut terpenes degradatio. (Z)- et Tagetone, [3588-18-9], [6752-80-3] sunt majores partes tagetarum. oleum. Solanone [1937-54-8] et pseudoionone [141-10-6] sunt acyclicC13 . ketoneswith terpenoideum sceletum. Solanone est unus e sapore-determinando constituunt tabaci et pseudoionone medium in synthesi of ionones.
usus	Synthesis organica; vilia unguenta, fla-voring.
Definition	Chebi: A heptenone id est hept-V-en-2-a yl coetus substituitur in situ 6. Est a oleum volatile componens oleum citronellae, oleum herbarum citreum et oleum palmarosum.
Praeparatio	Ex olei of* lemongrass aut ex citral refluxus pro XII horis in aqueum solutionem continens K2CO3, et subsequentem distillationem et fractionem vacuum; e* acetoacetic ester et yl-buten-3-ol-2 cum aluminio alcoholato in Carroll reactionem sequitur pyrolysis ester
Aroma limina values	Deprehensio: 50 ppb
Gustus limina values	Sapor notas ad 10 ppm: viridis, vegetativa, vitiata, pomum, Musa et viridia fabae similis.
salus Profile	Mediocriter toxicus per ingestion. Pellis irritamentum. Liquor flammabilis, cum calori expositus, scintillae, seu flamma. Cum calefacta compositione emittit fumum acrem et fumos exagitans.