Nerolidol manufacturers and suppliers

Nerolidol suppliers

Properties

Melting point:: -75 °C

Boiling point:: 114 °C/1 mmHg (lit.)

Density: 0.875 g/mL at 25 °C (lit.)

vapor pressure: <1 hPa (20 °C)

refractive index: n20/D 1.479(lit.)

FEMA: 2772 | NEROLIDOL (ISOMER UNSPECIFIED)

Flash point:: 230 °F

storage temp.: Store below +30°C.

solubility: 0.014g/l, Very slightly soluble in water, soluble in alcohol and oils.

pka: 14.44±0.29(Predicted)

form: Liquid

color: Clear slightly yellow

Specific Gravity: 0.88

Odor: at 100.00 %. floral green waxy citrus woody

Odor Type: floral

biological source: synthetic

explosive limit: 0.7-4.5%(V)

Water Solubility: immiscible

Merck: 14,6476

JECFA Number: 1646

BRN: 1724135

Henry's Law Constant: 3.2×10^-4 mol/(m³Pa) at 25℃, Copolovici and Niinemets (2015)

Cosmetics Ingredients Functions: PERFUMING

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+

InChIKey: FQTLCLSUCSAZDY-SDNWHVSQSA-N

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

LogP: 4.5 at 24℃

CAS DataBase Reference: 7212-44-4(CAS DataBase Reference)

NIST Chemistry Reference: 1,6,10-Dodecatrien-3-ol, 3,7,11-trimethyl-(7212-44-4)

EPA Substance Registry System: Nerolidol (7212-44-4)

Safety Information

Symbol(GHS): GHS07,GHS09

Signal word: Warning

Hazard statements: H317-H319-H410

Precautionary statements: P261-P264-P273-P280-P302+P352-P305+P351+P338

PPE: Eyeshields, Gloves, type ABEK (EN14387) respirator filter

Hazard Codes: Xi,N

Risk Statements: 36/37/38-50/53

Safety Statements: 26-36-61-60

RIDADR: UN 3082 9 / PGIII

WGK Germany: 2

RTECS: JR4977000

F: 10-23

Autoignition Temperature: 230 °C

TSCA: TSCA listed

HS Code: 29052290

Storage Class: 10 - Combustible liquids

Hazard Classifications: Aquatic Acute 1
Aquatic Chronic 1
Eye Irrit. 2
Skin Sens. 1B

Toxicity: LD50 orally in Rabbit: > 5000 mg/kg LD50 dermal Rabbit > 5000 mg/kg

REACH Registrations: Active

Use

Nerolidol is the sesquiterpene analog of linalool. Because of the double bond at the 6-position, it exists as (6Z)- and (6E)- isomers, each forming an enantiomeric pair, since the carbon atom in the 3-position is asymmetric. Nerolidol is a component of many essential oils. (3S,6E)-(+)-nerolidol occurs in cabreuva oil. Synthetic nerolidol consists of a mixture of racemic (6Z)- and (6E)-nerolidol and is a colorless liquid with a long-lasting, mild floral odor. Industrial synthesis of nerolidol starts with linalool, which is converted into geranylacetone by using diketene, ethyl acetoacetate, or isopropenyl methyl ether, analogously to the synthesis of 6-methyl-5-hepten-2-one from 2-methyl- 3-buten-2-ol. Addition of acetylene and partial hydrogenation of the resultant dehydronerolidol produces a mixture of (6Z)- and (6E)-nerolidol racemates.Nerolidol is used as a base note in many delicate floral odor complexes. It is also an intermediate in the production of vitamins E and K1.

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