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Documenti

18143

Supelco

trans-Nerolidol

analytical standard

Sinonimo/i:

(E)-3,7,11-Trimethyl-1,6,10-dodecatrien-3-ol, trans-3,7,11-Trimethyl-1,6,10-dodecatrien-3-ol

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About This Item

Formula condensata:
(CH3)2C=CHCH2CH2C(CH3)=CHCH2CH2C(CH3)(OH)CH=CH2
Numero CAS:
40716-66-3
Peso molecolare:
222.37
Beilstein:
5731231
Numero CE:
255-053-4
Numero MDL:
MFCD00008911
Codice UNSPSC:
85151701
ID PubChem:
329751635
NACRES:
NA.24

Grado

analytical standard

Livello qualitativo

100

Saggio

≥85% (GC)

Durata

limited shelf life, expiry date on the label

tecniche

HPLC: suitable
gas chromatography (GC): suitable

Indice di rifrazione

n20/D 1.479 (lit.)

P. eboll.

145-146 °C/12 mmHg (lit.)

Densità

0.876 g/mL at 25 °C (lit.)

applicazioni

food and beverages

Formato

neat

Stringa SMILE

C\C(C)=C/CC\C(C)=C\CCC(C)(O)C=C

InChI

1S/C15H26O/c1-6-15(5,16)12-8-11-14(4)10-7-9-13(2)3/h6,9,11,16H,1,7-8,10,12H2,2-5H3/b14-11+
FQTLCLSUCSAZDY-SDNWHVSQSA-N

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Descrizione generale

Nerolidol is a naturally occurring sesquiterpene found in the essential oils.

Applicazioni

It has been used as reference sample for analyzing sterols and related compounds in root bark of Oplopanax horridus using HPLC and TLC methods.
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Confezionamento

Bottomless glass bottle. Contents are inside inserted fused cone.

Pittogrammi

Exclamation markEnvironment
GHS07,GHS09

Avvertenze

Warning

Indicazioni di pericolo

H317,H319,H410

Classi di pericolo

Aquatic Acute 1 - Aquatic Chronic 1 - Eye Irrit. 2 - Skin Sens. 1B

Codice della classe di stoccaggio

10 - Combustible liquids

Classe di pericolosità dell'acqua (WGK)

WGK 1

Punto d’infiammabilità (°F)

235.4 °F - closed cup

Punto d’infiammabilità (°C)

113 °C - closed cup

Dispositivi di protezione individuale

Eyeshields, Gloves, type ABEK (EN14387) respirator filter

Choose from one of the most recent versions:

Certificati d'analisi (COA)

Lot/Batch Number
BCCL4307
BCCK9054
BCCK5865
BCCH2832
BCCD2160

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High-performance liquid chromatography and thin-layer chromatography assays for Devil's Club (Oplopanax horridus).
Gruber JW
Journal of Chromatographic Science, 42(4), 196-199 (2004)
Shigeru Tamogami et al.
FEBS letters, 585(12), 1807-1813 (2011-04-23)
DMNT biosynthesis was proposed to proceed via (E)-nerolidol in plants a decade ago. However, (E)-nerolidol function as airborne signal/substrate for in-vivo biosynthesis of DMNT remains to be investigated and the regulation of DMNT production and emission is largely unknown. We
Fernanda Pículo et al.
Journal of applied toxicology : JAT, 31(7), 633-639 (2010-11-23)
Nerolidol is a sesquiterpenoid component of essential oil used as a flavor and aroma enhancer. It has also been studied as a topical skin penetration enhancer, and has inhibitory activities against S. aureus and E. coli, among other activities. The
D McGinty et al.
Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association, 48 Suppl 3, S43-S45 (2010-02-10)
An addendum to the toxicologic and dermatologic review of Nerolidol (isomer unspecified) when used as a fragrance ingredient is presented.
S-Y Wang et al.
Insect molecular biology, 22(2), 172-182 (2013-01-09)
Olfaction plays an important role in insects' survival and reproduction. Odorant-binding proteins (OBPs) are considered to be one of the crucial proteins in the insect olfactory pathway. In this study, an antenna-specific OBP of the alfalfa plant bug, Adelphocoris lineolatus
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