Merck
Todas as fotos(2)

147524

Sigma-Aldrich

α-Pinene

98%

Sinônimo(s):
(±)-2-Pinene, alpha-Pinene, 2,6,6-Trimethylbicyclo[3.1.1]hept-2-ene
Empirical Formula (Hill Notation):
C10H16
Número CAS:
Peso molecular:
136.23
Número EC:
Número MDL:
ID de substância PubChem:
NACRES:
NA.22

Nível de qualidade

100

teor

98%

forma

liquid

temperatura de autoignição

491 °F

índice de refração

n20/D 1.465 (lit.)

pb

155-156 °C (lit.)

densidade

0.858 g/mL at 25 °C (lit.)

SMILES string

[H][C@@]12CC=C(C)[C@@]([H])(C1)C2(C)C

InChI

1S/C10H16/c1-7-4-5-8-6-9(7)10(8,2)3/h4,8-9H,5-6H2,1-3H3/t8-,9-/m1/s1

InChI key

GRWFGVWFFZKLTI-RKDXNWHRSA-N

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Descrição geral

α-Pinene is a chemical constituent of essential oil extracted from the stem of Canarium tramdenanum.
It reacts with ozone in the air to form oxygenated products that can further react to form secondary organic aerosols (SOA).

Aplicação

α-Pinene was used as standard in headspace solid-phase microextraction-gas chromatographic analysis of volatile compounds in virgin olive oils. It was used in the synthesis of cesium-doped heteropolyacid having potential application in biodiesel synthesis.

Embalagem

1 L in glass bottle
5, 250 mL in glass bottle

Palavra indicadora

Danger

Classificações de perigo

Aquatic Acute 1 - Aquatic Chronic 1 - Asp. Tox. 1 - Flam. Liq. 3 - Skin Irrit. 2 - Skin Sens. 1

Código de classe de armazenamento

3 - Flammable liquids

WGK

WGK 3

Ponto de fulgor (ºF)

87.8 °F - closed cup

Ponto de fulgor (ºC)

31 °C - closed cup

Equipamento de proteção individual

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

Certificado de análise

Insira o número de lote para pesquisar o Certificado de análise (COA).

Certificado de origem

Insira o número de lote para pesquisar o Certificado de origem (COO).

Newly characterized products and composition of secondary aerosols from the reaction of ?-pinene with ozone.
Jang M and Kamens R M
Atmospheric Environment, 33(3), 459-474 (1999)
Aerosol formation from the reaction of ?-pinene and ozone using a gas-phase kinetics-aerosol partitioning model.
Kamens R, et al.
Environmental Science & Technology, 33(9), 1430-1438 (1999)
Structure-activity relations in Cs-doped heteropolyacid catalysts for biodiesel production.
Narasimharao K, et al.
J. Catal., 248(2), 226-234 (2007)
Aleksandra Zielińska et al.
Pharmaceutical development and technology, 25(7), 832-844 (2020-03-25)
Glycerol monostearate solid lipid nanoparticles (SLN) were produced by hot high-pressure homogenization technique to load alpha-pinene, citral, geraniol or limonene. SLN were composed of 1 wt.% monoterpene, 4 wt.% of Imwitor® 900K as a solid lipid and 2.5 wt.% of Poloxamer188 as a
Jeremy D Allison et al.
Environmental entomology, 41(6), 1587-1596 (2013-01-17)
In recent years, several attractant pheromones have been identified for cerambycid beetles, including 2-(undecyloxy)-ethanol (hereafter monochamol) for Monochamus galloprovincialis (Olivier), M. alternatus Hope, and M. scutellatus (Say). This study screened eight known cerambycid pheromones or their analogues (including monochamol) as

Protocolos

GC Analysis of Geranium Bourbon Essential Oil on SUPELCOWAX® 10

-(+)-Limonene, purum, ≥98.0% (sum of enantiomers, GC); Geranyl tiglate; α-Terpineol, natural, ≥96%, FCC, FG; Geranyl formate; α-Pinene

Essential Oil on SLB®-5ms

Cinnamoµm Camphor, also known as the camphor tree, is grown in several parts of the world including Japan, Taiwan, and Australia. Camphor, which is used in medicinal and cosmetic preparations, is derived from the leaves and wood of this tree.

GC Analysis of Peppermint Essential Oil on SUPELCOWAX® 10

-Cymene; (−)-Menthone; α-Terpineol, natural, ≥96%, FCC, FG; Terpinolene; β-Bourbonene; 1-Octen-3-ol; β-Caryophyllene; Linalool; α-Terpinene; (−)-Menthol

GC Analysis of Spearmint Essential Oil on SLB®-IL59

-Cymene; Linalool; Menthol; α-Terpineol; Menthyl acetate

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