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Merck
CN

86485

萜品油烯

technical, ≥85% (GC)

别名:

4-异亚丙基-1-甲基环己烯, 对薄荷-1,4(8)-双烯, 对薄荷-1-烯-8-基-甲酸酯

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关于此项目

经验公式(希尔记法):
C10H16
化学文摘社编号:
分子量:
136.23
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
209-578-0
Beilstein/REAXYS Number:
1851203
MDL number:
Assay:
≥85% (GC)
Form:
liquid
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InChI key

MOYAFQVGZZPNRA-UHFFFAOYSA-N

InChI

1S/C10H16/c1-8(2)10-6-4-9(3)5-7-10/h4H,5-7H2,1-3H3

SMILES string

C\C(C)=C1/CCC(C)=CC1

vapor density

~4.7 (vs air)

vapor pressure

~0.5 mmHg ( 20 °C)

grade

technical

assay

≥85% (GC)

form

liquid

refractive index

n20/D 1.489 (lit.), n20/D 1.491

bp

184-185 °C (lit.)

density

0.861 g/mL at 25 °C (lit.)

Quality Level

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General description

松油烯是一种生物源性单萜。研究了 OH 和 NO 3 自由基与异松油烯气相反应的动力学。 黑曲霉 及几个相关菌种对异松油烯的生物转化已有报道。以氧化铝为多相催化剂,过氧化氢为氧化剂,研究了松油烯在无水物中的环氧化反应。它是从黄皮 地上部分提取的挥发油的主要成分

signalword

Danger

Hazard Classifications

Aquatic Acute 1 - Aquatic Chronic 3 - Asp. Tox. 1 - Skin Sens. 1

存储类别

3 - Flammable liquids

flash_point_f

141.8 °F - Seta closed cup

flash_point_c

61 °C - Seta closed cup

ppe

Eyeshields, Gloves, type ABEK (EN14387) respirator filter

法规信息

危险化学品
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历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Kinetics of the gas-phase reactions of hydroxyl and nitrogen oxide (NO3) radicals with 2-carene, 1, 8-cineole, p-cymene, and terpinolene.
Corchnoy SB and Atkinson R.
Environmental Science & Technology Letters, 24(10), 1497-1502 (1990)
Tran Huy Thaia et al.
Natural product communications, 9(10), 1531-1534 (2014-12-20)
The chemical composition of Vietnamese oil samples of the aerial parts of Clausena indica (Dalz.) Oliver and C. anisum-olens (Blanco) Merryll have been investigated using a combination of chromatographic and spectroscopic techniques. C. indica essential oil contained mainly terpinolene (53.9
Alumina as heterogeneous catalyst for the regioselective epoxidation of terpenic diolefins with hydrogen peroxide.
Uguina MA, et al.
J. Mol. Catal. A: Chem., 256(1), 208-215 (2006)
Biotransformation of monoterpenoids,(-)-and menthols, terpinolene and carvotanacetone by Aspergillus species.
Asakawa Y, et al.
Phytochemistry, 30(12), 3981-3987 (1991)
Michael F Russell et al.
Phytochemistry, 62(5), 683-689 (2003-03-07)
Individual leaves of the three most common chemotypes of Melaleuca alternifolia were examined both quantitatively and qualitatively for volatile constituents from the emergence of the first true leaves, through to 6-week-old tenth leaf set material. The 1,8-cineole and terpinolene chemotypes

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