Skip to Content
Merck
CN

B55203

(−)-Bornyl acetate

95%

Synonym(s):

endo-(1S)-1,7,7-Trimethylbicyclo[2.2.1]hept-2-yl acetate

Sign In to View Organizational & Contract Pricing

Select a Size

About This Item

Empirical Formula (Hill Notation):
C12H20O2
CAS Number:
5655-61-8
Molecular Weight:
196.29
Beilstein:
2502036
EC Number:
227-101-4
MDL number:
MFCD00867808
UNSPSC Code:
12352108
PubChem Substance ID:
329773262
NACRES:
NA.22

Key Documents

View All Documentation
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist

vapor pressure

0.6 mmHg ( 20 °C)

Quality Level

100

Assay

95%

form

liquid

optical activity

[α]20/D −38.10°, neat

refractive index

n20/D 1.463 (lit.)

bp

223-224 °C (lit.)

density

0.986 g/mL at 20 °C (lit.)

SMILES string

CC(=O)O[C@@H]1C[C@@H]2CC[C@@]1(C)C2(C)C

InChI

1S/C12H20O2/c1-8(13)14-10-7-9-5-6-12(10,4)11(9,2)3/h9-10H,5-7H2,1-4H3/t9-,10+,12+/m0/s1

InChI key

KGEKLUUHTZCSIP-HOSYDEDBSA-N

Looking for similar products? Visit Product Comparison Guide

Related Categories

Application

(−)-Bornyl acetate can be used:
  • As a key intermediate in the preparation of camphor.
  • To prepare (−)-englerin A, an anti-cancer agent.

Features and Benefits

Mimics the natural sex pheromone of the American cockroach.

Storage Class Code

10 - Combustible liquids

WGK

WGK 1

Flash Point(F)

185.0 - 194.0 °F

Flash Point(C)

85 - 90 °C

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
MKCZ1643
MKCZ1641
MKCX1855
MKCX1396
0000334981

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Search for a COA

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Bornyl acetate conversion enhancement by pervaporation in ionic liquid
Izak P, et al.
Planta Medica, 75(09), PI18-PI18 (2009)
Design and synthesis of terpene based englerin A mimics using chromium oxide mediated remote CH2 oxidation
Acerson MJ, et al.
Tetrahedron Letters, 56(23), 3277-3280 (2015)
Aldrichimica Acta, 16, 41-41 (1983)
Bénédicta G H Kpadonou Kpoviessi et al.
Journal of ethnopharmacology, 155(3), 1417-1423 (2014-07-25)
Different parts of Ocimum gratissimum Linn are largely used in folk medicine for the treatment of many diseases, some of which related to parasitical infections as fevers and headaches. In order to validate their use and to clarify the plant
Barbara Sgorbini et al.
Journal of chromatography. A, 1376, 9-17 (2014-12-30)
Herbs and spices are used worldwide as food flavoring, thus determination of their identity, origin, and quality is mandatory for safe human consumption. An analysis strategy based on separative (HS-SPME-GC-MS) and non-separative (HS-SPME-MS) approaches is proposed for the volatile fraction

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service