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ISOBORNYL FORMATE

CAS No.
1200-67-5
Chemical Name:
ISOBORNYL FORMATE
Synonyms
FEMA 2162;exo-1,7,7-;ISOBORNYL FORMATE;Formic acid isocamphyl ester;exo-1,7,7-trimethylbicyclo(2.2.1)hept-2;exo-1,7,7-trimethylbicyclo(2.2.1)hept-2r;exo-1,7,7-trimethylbicyclo(2.2.1)hept-2-yl;1,7,7-Trimethylbicyclo[2.2.1]hept-2-yl formate;exo-1,7,7-trimethylbicyclo(2.2.1)hept-2-ylformate;exo-1,7,7-Trimethylbicyclo(2.2.1)hept-2-ylformiat
CBNumber:
CB6248341
Molecular Formula:
C11H18O2
Molecular Weight:
182.26
MDL Number:
MFCD00135983
MOL File:
1200-67-5.mol
MSDS File:
SDS
Last updated:2026-05-28 02:14:39
Product description Number Pack Size Price
Isobornyl Formate min. 95.0 % I1253 250MG $246
rel-(1R,2R,4R)-1,7,7-trimethylbicyclo[2.2.1]heptan-2-yl formate 95% AD266192 250MG $170
rel-(1R,2R,4R)-1,7,7-trimethylbicyclo[2.2.1]heptan-2-yl formate 95% AD266192 1G $450
BICYCLO[2.2.1]HEPTAN-2-OL, 1,7,7-TRIMETHYL-, 2-FORMATE, (1R,2R,4R)-REL- 95% AA000PZC 100mg $105
BICYCLO[2.2.1]HEPTAN-2-OL, 1,7,7-TRIMETHYL-, 2-FORMATE, (1R,2R,4R)-REL- 95% AA000PZC 250mg $177
More product size

ISOBORNYL FORMATE Properties

Boiling point 213.6±7.0 °C(Predicted)
Density 1.02±0.1 g/cm3(Predicted)
FEMA 2162 | ISOBORNYL FORMATE
FLAVIS Number 09.176 | DL-Isobornyl formate
storage temp. Sealed in dry,Room Temperature
Odor at 100.00 %. camphor musty medical woody
Odor Type balsamic
JECFA Number 1390
Cosmetics Ingredients Functions PERFUMING
LogP 3.19
Substances Added to Food (formerly EAFUS) ISOBORNYL FORMATE
FDA 21 CFR 172.515
EWG's Food Scores 1
FDA UNII 8QPT973QF4
EPA Substance Registry System Bicyclo[2.2.1]heptan-2-ol, 1,7,7-trimethyl-, formate, (1R,2R,4R)-rel- (1200-67-5)

SAFETY

Risk and Safety Statements

Symbol(GHS)  Exclamation Mark (GHS07)
GHS07
Signal word  Warning
Hazard statements  H412-H315
Precautionary statements  P264-P280-P302+P352-P321-P332+P313-P362-P273-P501
TSCA  TSCA listed

ISOBORNYL FORMATE price

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
TCI Chemical I1253 Isobornyl Formate min. 95.0 % 1200-67-5 250MG $246 2026-04-30 Buy
ACHEMBLOCK AD266192 rel-(1R,2R,4R)-1,7,7-trimethylbicyclo[2.2.1]heptan-2-yl formate 95% 1200-67-5 250MG $170 2026-05-27 Buy
ACHEMBLOCK AD266192 rel-(1R,2R,4R)-1,7,7-trimethylbicyclo[2.2.1]heptan-2-yl formate 95% 1200-67-5 1G $450 2026-05-27 Buy
aablocks AA000PZC BICYCLO[2.2.1]HEPTAN-2-OL, 1,7,7-TRIMETHYL-, 2-FORMATE, (1R,2R,4R)-REL- 95% 1200-67-5 100mg $105 2026-05-25 Buy
aablocks AA000PZC BICYCLO[2.2.1]HEPTAN-2-OL, 1,7,7-TRIMETHYL-, 2-FORMATE, (1R,2R,4R)-REL- 95% 1200-67-5 250mg $177 2026-05-25 Buy
Product number Packaging Price Buy
I1253 250MG $246 Buy
AD266192 250MG $170 Buy
AD266192 1G $450 Buy
AA000PZC 100mg $105 Buy
AA000PZC 250mg $177 Buy

ISOBORNYL FORMATE Chemical Properties,Uses,Production

Aroma

ISOBORNYL FORMATE has green-earthy, herbaceous-camphoraceous odor, more piney than that of the Bornyl formate, and more camphor-like, less nutlike. Suggested for use in fruit flavors, and although this ester does have a sweet taste similar to that of Bornyl formate, it is overall less fruity or attractive. The use in fruit flavors amounts to a few ppm in the finished product (traces).

Description

Isobornyl formate has a characteristic aromatic, pine needles odor. May be prepared by reaction of formic acid with camphene in the presence of a catalyst; also in the absence of a catalyst; the resulting products do not exhibit well-defined optical characteristics. The corresponding optically active esters have been prepared from d- or ι-camphene and formic acid in the presence of phthalic anhydride.

Chemical Properties

Isobornyl formate has a characteristic aromatic, pine needles odor.

Preparation

By reaction of formic acid with camphene in the presence of a catalyst; also in the absence of a catalyst; the resulting products do not exhibit well-defined optical characteristics. The corresponding optically active esters have been prepared from d- or l-camphene and formic acid in the presence of phthalic anhydride

Definition

ChEBI: Isobornyl formate is a bornane monoterpenoid that is isoborneol in which the hydroxy hydrogen has been replaced by a formyl group. It has a role as a plant metabolite. It is a bornane monoterpenoid, a bridged compound and a formate ester. It is functionally related to a borneol.

ISOBORNYL FORMATE Preparation Products And Raw materials

Raw materials

Preparation Products

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ISOBORNYL FORMATE FEMA 2162 1,7,7-trimethyl-,formate,exo-bicyclo[2.2.1]heptan-2-o 1,7,7-Trimethylbicyclo[2.2.1]hept-2-yl formate Bicyclo[2.2.1]heptan-2-ol, 1,7,7-trimethyl-, formate, exo- exo-1,7,7- [(3S)-4,7,7-trimethyl-3-bicyclo[2.2.1]heptanyl] formate exo-1,7,7-trimethylbicyclo(2.2.1)hept-2 exo-1,7,7-trimethylbicyclo(2.2.1)hept-2r exo-1,7,7-trimethylbicyclo(2.2.1)hept-2-yl exo-1,7,7-trimethylbicyclo(2.2.1)hept-2-ylformate exo-1,7,7-Trimethylbicyclo[2.2.1]heptan-2-ylformiate Bicyclo2.2.1heptan-2-ol, 1,7,7-trimethyl-, formate, (1R,2R,4R)-rel- exo-1,7,7-Trimethylbicyclo(2.2.1)hept-2-ylformiat rel-Formic acid (1S*,2S*,4S*)-1,7,7-trimethylbicyclo[2.2.1]heptane-2-yl ester [(6S)-1,7,7-trimethyl-6-bicyclo[2.2.1]heptanyl] formate [(6S)-1,7,7-trimethyl-6-bicyclo[2.2.1]heptanyl] methanoate formic acid [(2S)-1,7,7-trimethylnorbornan-2-yl] ester Bicyclo[2.2.1]heptan-2-ol, 1,7,7-trimethyl-, 2-formate, (1R,2R,4R)-rel- rel-(1R,2R,4R)-1,7,7-Trimethylbicyclo[2.2.1]heptan-2-yl formate Formic acid isocamphyl ester 1200-67-5