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W277207

Sigma-Aldrich

Nerolidol

mixture of cis and trans, ≥97%, stabilized, FG

Sinonimo/i:

3,7,11-Trimethyl-1,6,10-dodecatrien-3-ol, 3-Hydroxy-3,7,11-trimethyl-1,6,10-dodecatriene

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About This Item

Formula condensata:
(CH3)2C=CHCH2CH2C(CH3)=CHCH2CH2C(CH3)(OH)CH=CH2
Numero CAS:
7212-44-4
Peso molecolare:
222.37
Numero FEMA:
2772
Numero CE:
230-597-5
N° CoE:
67
Numero MDL:
MFCD00008911
Codice UNSPSC:
12164502
ID PubChem:
24901317
Numero Flavis:
2.018
NACRES:
NA.21

Origine biologica

synthetic

Livello qualitativo

400

Grado

FG
Kosher

agenzia

meets purity specifications of JECFA

Conformità normativa

EU Regulation 1334/2008 & 872/2012
FCC
FDA 21 CFR 172.515

Saggio

≥97%

contiene

synthetic α-tocopherol as stabilizer

Indice di rifrazione

n20/D 1.479 (lit.)

P. eboll.

114 °C/1 mmHg (lit.)

Densità

0.875 g/mL at 25 °C (lit.)

applicazioni

flavors and fragrances

Documentazione

see Safety & Documentation for available documents

Allergene alimentare

no known allergens

Organolettico

green; floral; woody

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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Applicazioni


  • Effects of Six Natural Compounds and Their Derivatives on the Control of Coccidiosis in Chickens.: This article discusses the use of natural compounds including nerolidol for controlling coccidiosis in poultry, indicating its applications in veterinary biochemistry and animal health (Hou et al., 2024).

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. 1

Codice della classe di stoccaggio

10 - Combustible liquids

Classe di pericolosità dell'acqua (WGK)

WGK 2

Punto d’infiammabilità (°F)

262.4 °F - closed cup

Punto d’infiammabilità (°C)

128 °C - closed cup

Dispositivi di protezione individuale

Eyeshields, Gloves, type ABEK (EN14387) respirator filter

Certificati d'analisi (COA)

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A Lapczynski et al.
Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association, 46 Suppl 11, S247-S250 (2008-07-22)
A toxicologic and dermatologic review of nerolidol when used as a fragrance ingredient is presented.
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
Clécio S Ramos et al.
Journal of insect physiology, 58(12), 1663-1668 (2012-10-31)
The chemical volatiles from plant leaves and their biological activities have been extensively studied. However, no studies have addressed plant-chemical volatiles after undergoing the digestive process in host insects. Here we describe for the first time chemical profiles of volatile
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
Jianrong Wei et al.
Journal of chemical ecology, 44(7-8), 637-649 (2018-06-30)
We performed single-sensillum recordings from male and female antennae of the Asian longhorned beetle, Anoplophora glabripennis, that included as stimuli the two components of this species' aggregation-sex pheromone in addition to various general odorants. We compared the aggregation-sex-pheromone-component responses of
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