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H12900

Sigma-Aldrich

cis-3-esene-1-ol

98%

Sinonimo/i:

(3Z)-3-Hexen-1-ol, (Z)-3-Hexen-1-ol, (Z)-Hex-3-en-1-ol, 3Z-Hexen-1-ol, Blaetteralkohol, cis-1-Hydroxy-3-hexene, cis-3-Hexene-1-ol, cis-3-Hexenol

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About This Item

Formula condensata:
C2H5CH=CHCH2CH2OH
Numero CAS:
928-96-1
Peso molecolare:
100.16
Beilstein:
1719712
Numero CE:
213-192-8
Numero MDL:
MFCD00063217
Codice UNSPSC:
12352100
ID PubChem:
24895448
NACRES:
NA.22

Densità del vapore

3.45 (vs air)

Saggio

98%

Forma fisica

liquid

Colore

APHA: ≤100

Indice di rifrazione

n20/D 1.44 (lit.)

P. eboll.

156-157 °C (lit.)

Densità

0.848 g/mL at 25 °C (lit.)

Stringa SMILE

CC\C=C/CCO

InChI

1S/C6H12O/c1-2-3-4-5-6-7/h3-4,7H,2,5-6H2,1H3/b4-3-
UFLHIIWVXFIJGU-ARJAWSKDSA-N

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Categorie correlate

Pittogrammi

Flame
GHS02

Avvertenze

Warning

Indicazioni di pericolo

H226

Classi di pericolo

Flam. Liq. 3

Codice della classe di stoccaggio

3 - Flammable liquids

Classe di pericolosità dell'acqua (WGK)

WGK 1

Punto d’infiammabilità (°F)

111.2 °F - closed cup

Punto d’infiammabilità (°C)

44 °C - closed cup

Dispositivi di protezione individuale

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

Certificati d'analisi (COA)

Cerca il Certificati d'analisi (COA) digitando il numero di lotto/batch corrispondente. I numeri di lotto o di batch sono stampati sull'etichetta dei prodotti dopo la parola ‘Lotto’ o ‘Batch’.

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trans-2-Hexen-1-ol ≥95%, FCC, FG

Sigma-Aldrich

W256218

trans-2-Hexen-1-ol

cis-3-Hexenyl acetate ≥98%, stabilized, FCC, FG

Sigma-Aldrich

W317101

cis-3-Hexenyl acetate

trans-2-Hexen-1-al 98%

Sigma-Aldrich

132659

trans-2-Hexen-1-al

4-Hexen-1-ol, predominantly trans 97%

Sigma-Aldrich

237604

4-Hexen-1-ol, predominantly trans

Supelco

Supelco

CRM47522

(±)-Geosmin solution

Damascenone analytical standard

Supelco

41163

Damascenone

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Journal of comparative physiology. A, Neuroethology, sensory, neural, and behavioral physiology, 194(5), 501-515 (2008-04-05)
Pheromone-source orientation behavior can be modified by coexisting plant volatiles. Some host plant volatiles enhance the pheromonal responses of olfactory receptor neurons and increase the sensitivity of orientation behavior in the Lepidoptera species. Although many electrophysiological studies have focused on
Damon J Crook et al.
Journal of economic entomology, 105(2), 429-437 (2012-05-23)
Field trapping assays were conducted in 2009 and 2010 throughout western Michigan, to evaluate lures for adult emerald ash borer, A. planipennis Fairmaire (Coleoptera: Buprestidae). Several ash tree volatiles were tested on purple prism traps in 2009, and a dark
Andre F Cruz et al.
Phytochemistry, 78, 72-80 (2012-04-24)
Fusarium diseases cause major economic losses in wheat-based crop rotations. Volatile organic compounds (VOC) in wheat and rotation crops, such as chickpea, may negatively impact pathogenic Fusarium. Using the headspace GC-MS method, 16 VOC were found in greenhouse-grown wheat leaves:
L Chen et al.
Bulletin of entomological research, 97(5), 515-522 (2007-10-06)
Parasitoids employ different types of host-related volatile signals for foraging and host-location. Host-related volatile signals can be plant-based, originate from the herbivore host or produced from an interaction between herbivores and their plant host. In order to investigate potential sex-
Tsviya Olender et al.
Chemical senses, 37(7), 581-584 (2012-06-15)
Considerable evidence supports the idea that odorant recognition depends on specific sequence variations in olfactory receptor (OR) proteins. Much of this emerges from in vitro screens in heterogenous expression systems. However, the ultimate proof should arise from measurements of odorant
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