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D7151

Sigma-Aldrich

1,7-Dioxaspiro[5.5]undecane

≥97%

Synonym(s):

Olive-fly ketal

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About This Item

Empirical Formula (Hill Notation):
C9H16O2
CAS Number:
180-84-7
Molecular Weight:
156.22
EC Number:
205-870-7
MDL number:
MFCD00011578
UNSPSC Code:
12352100
PubChem Substance ID:
57654121
NACRES:
NA.22

Assay

≥97%

form

liquid

refractive index

n20/D 1.464 (lit.)

bp

193 °C/750 mmHg (lit.)

density

1.02 g/mL at 25 °C (lit.)

storage temp.

2-8°C

SMILES string

C1CCC2(CCCCO2)OC1

InChI

1S/C9H16O2/c1-3-7-10-9(5-1)6-2-4-8-11-9/h1-8H2

InChI key

GBBVHDGKDQAEOT-UHFFFAOYSA-N

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Biochem/physiol Actions

Pheromone for Dacus oleae

Storage Class Code

10 - Combustible liquids

WGK

WGK 3

Flash Point(F)

147.2 °F - closed cup

Flash Point(C)

64 °C - closed cup

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

FSL

Group 4: Flammable liquids
Type 2 petroleums
Hazardous rank III
Water insoluble liquid

JAN Code

D7151-100MG:
D7151-500MG:
D7151-BULK:
D7151-VAR:

Certificates of Analysis (COA)

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Anat Levi-Zada et al.
Journal of chemical ecology, 38(8), 1036-1041 (2012-09-04)
The olive fruit fly, Bactrocera oleae (Diptera: Tephritidae), uses 1,7-dioxaspiro[5.5]undecane ("olean"), produced primarily by females, as a sex pheromone. We used sequential solid phase microextraction-gas chromatography mass spectrometry (SPME-GCMS) analysis to show that female olive flies release about 1000 ng
N Rysanek et al.
Acta crystallographica. Section C, Crystal structure communications, 52 ( Pt 11), 2932-2936 (1996-11-15)
The complex beta-cyclodextrin-1,7-dioxaspiro[5,5]undecane nonahydrate, C42H70O35.C9H16O2.9H2O, belongs to the class of beta-cyclodextrin dimeric-type complexes. The racemic guest molecule is present in a disordered position. Both enantiomers are located in two different regions inside the channel formed by the host dimers.
Brett D Schwartz et al.
Organic letters, 7(6), 1173-1176 (2005-03-12)
[reaction: see text] A biosynthetic scheme rationalizing the formation of (+/-)-1,7-dioxaspiro[5.5]undecane (5) in the fruit fly species Bactrocera cacuminata and Bactrocera oleae (olive fruit fly) is presented. Incorporation studies with deuterium-labeled keto aldehyde (10), 1,5-nonanediol (11), and 1,5,9-nonanetriol (12), and
S Makedonopoulou et al.
Acta crystallographica. Section B, Structural science, 57(Pt 3), 399-409 (2001-05-25)
The enantiomers of racemic olive fly sex pheromone 1,7-dioxaspiro[5.5]undecane (1) have been isolated by crystallization with enantiospecific cyclodextrin hosts: (S)-(1) crystallizes with heptakis(2,3,6-tri-O-methyl)-beta-cyclodextrin (TMbetaCD) and (R)-(1) with hexakis(2,3,6-tri-O-methyl)-alpha-cyclodextrin (TMalphaCD). The crystal structure of TMbetaCD/(S)-(1) from synchrotron radiation data at 100
Abby Jones Weldon et al.
The Journal of organic chemistry, 71(24), 9212-9216 (2006-11-18)
The relative gas-phase energetics of several low-lying isomers of 1,7-dioxaspiro[5.5]undecane and 1,7,9-trioxadispiro[5.1.5.3]hexadecane have been calculated with second-order Mller-Plesset perturbation theory and basis sets as large as aug-cc-pVQZ. Relative energies in THF, dichloromethane, acetone, and DMSO have been estimated with corrections
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