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Merck

442505

Supelco

莰烯

analytical standard

别名:

DL-莰烯

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About This Item

经验公式(希尔记法):
C10H16
CAS号:
分子量:
136.23
EC號碼:
MDL號碼:
分類程式碼代碼:
12000000
PubChem物質ID:

等級

analytical standard

品質等級

CofA

current certificate can be downloaded

包裝

ampule of 1000 mg

技術

HPLC: suitable
gas chromatography (GC): suitable

bp

159-160 °C (lit.)

mp

48-52 °C (lit.)

密度

0.85 g/mL at 25 °C (lit.)

應用

cleaning products
cosmetics
environmental
flavors and fragrances
food and beverages
personal care

格式

neat

儲存溫度

2-30°C

SMILES 字串

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

InChI

1S/C10H16/c1-7-8-4-5-9(6-8)10(7,2)3/h8-9H,1,4-6H2,2-3H3/t8-,9+/m0/s1

InChI 密鑰

CRPUJAZIXJMDBK-DTWKUNHWSA-N

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一般說明

莰烯为用于草药产品,营养食品和研究的各种药用植物提供了广泛且快速增长的活性成分和标志化合物的分析标准品组合。莰烯是一种环状单萜,是胡椒(Piper hymenophyllum Miq),伞形科物种,苍耳等精油的重要成分。据报告,它还被称为现代月季 奇唇兰兰花物种等的香料成分。据报告,莰烯用于香水工业,其天然来源是唇形科Satureja douglasii)。
莰烯是一种有机塑料型的晶体,可作为工业中间化合物用于生产樟脑,乙酸异冰片酯和异冰片等商业化学品。它可以通过α-蒎烯在酸性二氧化钛催化剂上的异构化而获得。

應用

有关合适的仪器技术的更多信息,请参阅产品的分析证书。想要获得更多支持,请联系技术服务部。
莰烯可用作分析标准品,用于使用气相色谱-质谱法(GC-MS)定量测定 现代月季和鱼样品中的分析物。

訊號詞

Danger

危險聲明

危險分類

Aquatic Acute 1 - Aquatic Chronic 1 - Eye Irrit. 2 - Flam. Sol. 1

儲存類別代碼

4.1B - Flammable solid hazardous materials

水污染物質分類(WGK)

WGK 2

閃點(°F)

78.8 °F - DIN 51755 Part 1

閃點(°C)

26 °C - DIN 51755 Part 1

個人防護裝備

Eyeshields, Gloves, type P3 (EN 143) respirator cartridges


从最新的版本中选择一种:

分析证书(COA)

Lot/Batch Number

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其他客户在看

Slide 1 of 3

1 of 3

Phytochemical composition and in vitro antimicrobial activity of essential oil of Piper hymenophyllum Miq.: A rare wild betel
Ratnam VK, et al.
International Journal of Pharmacognosy and Phytochemical Research , 7(1), 68-71 (2015)
Ion exchange resins as catalyst for the isomerization of ?-pinene to camphene
Chimal-Valencia.O, et al.
BioTechnology: An Indian Journal, 93, 119-123 (2004)
Determination of fragrance ingredients in fish by ultrasound-assisted extraction followed by purge & trap
Chen LC, et al.
Analytical Methods : Advancing Methods and Applications, 9(15), 2237-2245 (2017)
Dendritic growth kinetics and structure II. Camphene
Rubinstein.RE and Glicksman.EM
Journal of Crystal Growth, 112, 97-110 (1991)
M Tiwari et al.
Toxicology in vitro : an international journal published in association with BIBRA, 23(2), 295-301 (2009-01-13)
Exploration of antioxidants of plant origin and scientific validation of their efficacies has unraveled bioactives from natural sources. In this study, two terpenoids camphene and geraniol were assessed for their cytoprotective and antioxidant potential using t-BHP stressed rat alveolar macrophages.

实验方案

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.

Cymene; 4,5,6,7-Tetrahydro-3,6-dimethylbenzofuran; Linalool; Menthol; Menthone; Menthyl acetate; Germacrene D; Bicyclogermacrene; Thymol

-α-Bergamotene; β-Bisabolene; α-Terpineol; Neryl acetate; Geranyl acetate; Neral; Geranial

-3,7-Dimethyl-2,6-octadien-1-ol; Neral; Geraniol; Geranial; Undecanal; Citronellyl acetate; Neryl acetate; 3,7-Dimethyl-2,6-octadienyl acetate; 1-Tetradecene; Tetradecane; α-Bisabolol

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