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00459

Supelco

Nerolidol

mixture of cis and trans, analytical standard

Synonym(s):

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

Linear Formula:
(CH3)2C=CHCH2CH2C(CH3)=CHCH2CH2C(CH3)(OH)CH=CH2
CAS Number:
7212-44-4
Molecular Weight:
222.37
EC Number:
230-597-5
MDL number:
MFCD00008911
UNSPSC Code:
85151701
PubChem Substance ID:
329747073
NACRES:
NA.24

Quality Level

100

grade

analytical standard

Assay

≥98.5% (GC)

shelf life

limited shelf life, expiry date on the label

impurities

≤0.3% water

refractive index

n20/D 1.478-1.483
n20/D 1.479 (lit.)

bp

114 °C/1 mmHg (lit.)

density

0.875 g/mL at 25 °C (lit.)

application(s)

cleaning products
cosmetics
flavors and fragrances
food and beverages
personal care

format

neat

SMILES string

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+

InChI key

FQTLCLSUCSAZDY-SDNWHVSQSA-N

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General description

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

Pictograms

Exclamation markEnvironment
GHS07,GHS09

Signal Word

Warning

Hazard Statements

H317,H319,H410

Hazard Classifications

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

Storage Class Code

10 - Combustible liquids

WGK

WGK 2

Flash Point(F)

262.4 °F - closed cup

Flash Point(C)

128 °C - closed cup

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Certificates of Analysis (COA)

Lot/Batch Number
BCCF2485
BCCB7487
BCBZ4371
BCBX3851
BCBW8263

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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.
A Lapczynski et al.
Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association, 46 Suppl 11, S245-S246 (2008-07-22)
A toxicologic and dermatologic review cis-nerolidol when used as a fragrance ingredient is presented.
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.
Tiago Coelho de Assis Lage et al.
Experimental parasitology, 148, 24-29 (2014-12-03)
Baccharis dracunculifolia DC (common name "alecrim-do-campo" in Brazil) is a plant with widespread distribution in South America that is the botanical origin of green propolis. The aim of this study was to evaluate the chemical composition and acaricidal activity of
J A R Curvelo et al.
Journal of medical microbiology, 63(Pt 5), 697-702 (2014-02-14)
Candidiasis is a major opportunistic fungal infection in humans, and its incidence has increased steadily over the last two decades. Candida albicans, the main species of the genus, has a large arsenal of virulence attributes that contribute to successful infections
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