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136913

Sigma-Aldrich

3-Octanone

≥98%

Sinonimo/i:

Ethyl amyl ketone, Ethyl pentyl ketone

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About This Item

Formula condensata:
CH3(CH2)4COC2H5
Numero CAS:
106-68-3
Peso molecolare:
128.21
Beilstein:
1700021
Numero CE:
203-423-0
Numero MDL:
MFCD00009515
Codice UNSPSC:
12352100
ID PubChem:
24848302
NACRES:
NA.22

Livello qualitativo

100

Saggio

≥98%

Stato

liquid

Indice di rifrazione

n20/D 1.415 (lit.)

P. ebollizione

167-168 °C (lit.)

Densità

0.822 g/mL at 25 °C (lit.)

Gruppo funzionale

ketone

Stringa SMILE

CCCCCC(=O)CC

InChI

1S/C8H16O/c1-3-5-6-7-8(9)4-2/h3-7H2,1-2H3
RHLVCLIPMVJYKS-UHFFFAOYSA-N

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Descrizione generale

3-Octanone is the common metabolite produced by some fungal species.

Applicazioni

3-Octanone was used to study the effect TiO2 photocatalyst on the rate and the ratio of products generated in photocatalytic oxidation of 3-octanone.

Pittogrammi

FlameExclamation mark
GHS02,GHS07

Avvertenze

Warning

Indicazioni di pericolo

H226,H315

Classi di pericolo

Flam. Liq. 3 - Skin Irrit. 2

Codice della classe di stoccaggio

3 - Flammable liquids

Classe di pericolosità dell'acqua (WGK)

WGK 1

Punto d’infiammabilità (°F)

123.8 °F - closed cup

Punto d’infiammabilità (°C)

51 °C - closed cup

Dispositivi di protezione individuale

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

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Certificati d'analisi (COA)

Lot/Batch Number
SHBP3039
SHBL9885
MKCG0132
MKBQ0220V
MKBK3944V

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2-Octanone analytical standard

Supelco

02479

2-Octanone

3-Octanol ≥97%, FCC, FG

Sigma-Aldrich

W358118

3-Octanol

2-Octanone ≥98%, FG

Sigma-Aldrich

W280208

2-Octanone

1-Octen-3-ol ≥98%, FCC, FG

Sigma-Aldrich

W280518

1-Octen-3-ol

2-Nonanone ≥99%, FCC, FG

Sigma-Aldrich

W278505

2-Nonanone

4-Heptanone 98%

Sigma-Aldrich

101745

4-Heptanone

2-Heptanone 99%

Sigma-Aldrich

537683

2-Heptanone

Ocimene mixture of isomers, stabilized, ≥90%

Sigma-Aldrich

W353901

Ocimene

3-Phenylpropionaldehyde for synthesis

Sigma-Aldrich

8.04542

3-Phenylpropionaldehyde

Effects of water, salt water, and silicone overcoating of the TiO2 photocatalyst on the rates and products of photocatalytic oxidation of liquid 3-octanol and 3-octanone.
Sunada F and Heller A.
Environmental Science & Technology, 32(2), 282-286 (1998)
A L Sunesson et al.
The Annals of occupational hygiene, 40(4), 397-410 (1996-08-01)
Two fungal species commonly found in indoor environments, Penicillium commune and Paecilomyces variotü, were cultivated on pine wood and on a combination of gypsum board and mineral wool. Air from the cultures was adsorbed on Tenax TA and analysed using
D Tuma et al.
International journal of food microbiology, 8(2), 103-119 (1989-05-01)
Western hard red spring wheat, stored at 20 and 25% moisture contents for 10 months during 1985-86, was monitored for biotic and abiotic variables in 10 unheated bins in Winnipeg, Manitoba. The major odor volatiles identified were 3-methyl-1-butanol, 3-octanone and
Martin J Schnermann et al.
Proceedings of the National Academy of Sciences of the United States of America, 107(14), 6158-6163 (2010-03-25)
Golgi-modifying properties of the spongian diterpene macfarlandin E (MacE) and a synthetic analog, t-Bu-MacE, containing its 2,7-dioxabicyclo[3.2.1]octan-3-one moiety are reported. Natural product screening efforts identified MacE as inducing a novel morphological change in Golgi structure defined by ribbon fragmentation with
Marek Nemcovic et al.
FEMS microbiology letters, 284(2), 231-236 (2008-05-31)
Light and starvation are two principal environmental stimuli inducing conidiation in the soil micromycete Trichoderma spp. We observed that volatiles produced by conidiating colonies of Trichoderma spp. elicited conidiation in colonies that had not been induced previously by exposure to
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