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141-12-8

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141-12-8 Usage

Description

Neryl acetate has a very sweet, floral, orange-blossom and roselike odor. It is initially fresh and pungent, and then a honey-like flavor with a raspberry undertone. Neryl acetate may be prepared by esterification of nerol with acetic acid; also prepared from myrcene by hydrobromination and esterification.

Chemical Properties

Different sources of media describe the Chemical Properties of 141-12-8 differently. You can refer to the following data:
1. Neryl acetate has a very sweet, floral, orange-blossom and rose-like odor. It has a flavor that is initially fresh and pungent, and then honey-like with a raspberry undertone
2. CLEAR COLOURLESS TO SLIGHTLY YELLOWISH LIQUID
3. is the (Z)- isomer of geranyl acetate. It is present in helichrysum oil and has also been identified in, among others, neroli oil and petitgrain oil Bigarade. It is a colorless, floral, sweet-smelling liquid and is used in perfumery for blossom compositions (e.g., orange blossom and jasmine).

Occurrence

Reported found in the essential oils of lemon, neroli, and petitgrain bigarade, in sweet and bitter orange, lemon, grapefruit, lime, black currants, grapes, celery, ginger, Mentha oils, nutmeg, thyme, hop oil, white wine, cocoa, tea, passion fruit, sweet marjoram, cardamom, lovage leaf, myrtle leaf and berry, buchu oil, lemon balm, clary sage, eucalyptus oil and mastic gum leaf oil

Preparation

By esterification of nerol with acetic acid; also prepared from myrcene by hydrobromination and esterification.

Aroma threshold values

Detection: 2 to 8.5 ppm

Taste threshold values

Taste characteristics at 10 ppm: floral, rosy, soapy, fruity, pear, and tropical.

General Description

cis-3,7-Dimethyl-2,6-octadien-1-yl acetate (Neryl acetate) is the major component of lavender volatile oils.

Biochem/physiol Actions

Taste at 5 ppm

Check Digit Verification of cas no

The CAS Registry Mumber 141-12-8 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 1,4 and 1 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 141-12:
(5*1)+(4*4)+(3*1)+(2*1)+(1*2)=28
28 % 10 = 8
So 141-12-8 is a valid CAS Registry Number.
InChI:InChI=1/C12H20O2/c1-10(2)6-4-7-11(3)8-5-9-12(13)14/h6,8H,4-5,7,9H2,1-3H3,(H,13,14)/p-1

141-12-8 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
  • Packaging
  • Price
  • Detail
  • TCI America

  • (N0463)  Neryl Acetate  >95.0%(GC)

  • 141-12-8

  • 25mL

  • 250.00CNY

  • Detail
  • Alfa Aesar

  • (A19282)  Neryl acetate, 98%   

  • 141-12-8

  • 25g

  • 328.0CNY

  • Detail
  • Alfa Aesar

  • (A19282)  Neryl acetate, 98%   

  • 141-12-8

  • 100g

  • 953.0CNY

  • Detail
  • Sigma-Aldrich

  • (46015)  Nerylacetate  analytical standard

  • 141-12-8

  • 46015-1ML

  • 1,027.26CNY

  • Detail

141-12-8SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name Neryl Acetate

1.2 Other means of identification

Product number -
Other names 2,6-Octadien-1-ol, 3,7-dimethyl-, acetate, (Z)-

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only. Food additives -> Flavoring Agents
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:141-12-8 SDS

141-12-8Related news

OsO 4 -Catalyzed oxidative cyclization of geranyl and NERYL ACETATE (cas 141-12-8) to cis-2,5-bis(hydroxymethyl)tetrahydrofurans10/01/2019

OsO 4 catalyzes the oxidative cyclization of the 1,5-dienes geranyl acetate (1) and neryl acetate (2) to the cis-2,5-bis(hydroxymethyl)tetrahydrofurans 3 and 4 respectively, in the presence of NaIO 4 as cooxidant in DMF. The reaction is stereospecific and proceeds with the sequen...detailed

141-12-8Relevant articles and documents

Epoxy-Tethered Diels-Alder Reaction toward the Tricyclic Core of Kalihinols

Krishna Chaitanya, Nandikolla,Dinda, Shrabani,Mainkar, Prathama S.,Chandrasekhar, Srivari

, p. 3557 - 3560 (2020)

A chiral-template-driven intramolecular Diels-Alder reaction has been used to build the tricyclic core of kalihinols, a group of antimalarial marine natural products. The key starting materials are commercially available nerol and sulcatone.

Synthesis of a model DEF-ring core of hexacyclinic acid

Clarke, Paul A.,Grist, Matthew,Ebden, Mark,Wilson, Claire

, p. 1560 - 1561 (2003)

The first synthesis of a DEF-ring system of hexacyclinic acid is reported. The key steps being an intramolecular Pd(0) π-allyl substitution reaction, followed by a transannular iodocyclisation with acetyl hypoiodite.

Total Synthesis of Isohericenone J via a Stille Coupling Reaction

Cao, Wei,Chen, Ping,Tang, Yu

, p. 1701 - 1705 (2020/06/08)

The first total synthesis of isohericenone J is reported. Key features of this synthetic strategy are a Friedel-Crafts reaction to construct the isobenzofuranone unit and a Pd-catalyzed Stille coupling reaction for the formation of the C5-C1′ bond, generating the natural product, as well as one of its isomers, in 6.0% overall yield in eight steps. This strategy provides a foundation for the synthesis of challenging isobenzofuranone and isoindolinone-type derivatives.

New neryl esters from Helichrysum italicum (Roth) G. Don (Asteraceae) essential oil

?or?evi?, Miljana R.,?ivkovi? Sto?i?, Milena Z.,Aksi?, Jelena M.,Gen?i?, Marija S.,Mladenovi?, Marko Z.,Radulovi?, Niko S.

supporting information, (2020/11/02)

Helichrysum italicum (immortelle) is a dwarf aromatic shrub native to the Mediterranean region. The typical subspecies (italicum) produces an essential oil rich in neryl acetate and characteristic β-diketones, italidiones, highly valued in the perfume industry. As esters are an important group of aroma-active volatiles, herein the composition of the ester fraction of this immortelle chemotype essential oil was studied in detail. Chromatographic separation of Corsican immortelle essential oil enabled the discovery of numerous potentially olfactory-interesting esters of nerol and/or angelic acid, undetectable by direct GC-MS analyses of the unfractioned oil. Four esters of nerol and medium-chain branched fatty acids represent new natural products, while several other esters have a rather restricted occurrence in the Plant Kingdom.

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