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Merck

W285609

Sigma-Aldrich

α-フェランドレン

≥75%, stabilized

別名:

2-メチル-5-(1-メチルエチル)-1,3-シクロヘキサジエン

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About This Item

実験式(ヒル表記法):
C10H16
CAS番号:
分子量:
136.23
FEMA番号:
2856
EC Number:
欧州評議会番号:
2117
MDL番号:
UNSPSCコード:
12164502
PubChem Substance ID:
Flavis 番号:
1.006
NACRES:
NA.21

由来生物

synthetic

品質水準

グレード

Halal
Kosher

法規制遵守

FDA 21 CFR 172.515

アッセイ

≥75%

光学活性

[α]20/D −139 to −110°, neat

含みます

alpha-tocopherol as additive

屈折率

n20/D 1.474 (lit.)

密度

0.85 g/mL at 25 °C (lit.)

アプリケーション

flavors and fragrances

文書

see Safety & Documentation for available documents

食物アレルゲン

no known allergens

官能

spicy; woody

SMILES記法

CC(C)C1CC=C(C)C=C1

InChI

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

InChI Key

OGLDWXZKYODSOB-UHFFFAOYSA-N

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関連するカテゴリー

アプリケーション


  • Does green mean clean Volatile organic emissions from regular versus green cleaning products.: This research compares the volatile organic compound (VOC) emissions from conventional and green cleaning products, identifying a-phellandrene as a common component. The findings highlight the environmental impact of green products and their effectiveness (Harding-Smith et al., 2024).

  • RNA-Seq-Based Transcriptomics and GC-MS Quantitative Analysis Reveal Antifungal Mechanisms of Essential Oil of Clausena lansium (Lour.) Skeels Seeds against Candida albicans.: The study uses RNA-Seq and GC-MS to investigate the antifungal properties of Clausena lansium essential oil, which contains a-phellandrene, against Candida albicans, providing insights into its potential therapeutic applications (Ma et al., 2023).

  • Unveiling the Anti-Cholera and Active Diabetic Renoprotective Compounds of Maqian Essential Oil: A Computational and Molecular Dynamics Study.: This study identifies a-phellandrene as an active compound in Maqian essential oil with anti-cholera and renoprotective effects, suggesting its potential for treating cholera and protecting against diabetic renal damage (Dahab et al., 2023).

  • Electrophysiological and Behavioral Responses of Batocera horsfieldi Hope to Volatiles from Pistacia chinensis Bunge.: This research examines the responses of Batocera horsfieldi to volatiles, including a-phellandrene, from Pistacia chinensis. The findings have implications for pest management strategies using natural volatiles (Fan et al., 2023).

免責事項

研究開発またはEUを除く食品用途向けです。小売販売用ではありません。

ピクトグラム

FlameHealth hazard

シグナルワード

Danger

危険有害性情報

危険有害性の分類

Asp. Tox. 1 - Flam. Liq. 3

保管分類コード

3 - Flammable liquids

WGK

WGK 2

引火点(°F)

116.6 °F - closed cup

引火点(℃)

47 °C - closed cup

個人用保護具 (PPE)

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


適用法令

試験研究用途を考慮した関連法令を主に挙げております。化学物質以外については、一部の情報のみ提供しています。 製品を安全かつ合法的に使用することは、使用者の義務です。最新情報により修正される場合があります。WEBの反映には時間を要することがあるため、適宜SDSをご参照ください。

消防法

第4類:引火性液体
第二石油類
危険等級III
非水溶性液体

Jan Code

W285609-BULK-K:
W285609-SAMPLE:
W285609-BULK:
W285609-VAR-K:
W285609-8KG-K:4548173312125
W285609-20KG-K:4548173312095
W285609-4KG-K:4548173312101
W285609-1KG-K:4548173312088
W285609-8KG:
W285609-800G:
W285609-800G-K:4548173312118
W285609-1KG:
W285609-SAMPLE-K:
W285609-20KG:
W285609-4KG:


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試験成績書(COA)

Lot/Batch Number

適切なバージョンが見つかりませんか。

特定のバージョンが必要な場合は、ロット番号またはバッチ番号で特定の証明書を検索できます。

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Slide 1 of 7

1 of 7

ミルセン analytical standard

Supelco

64643

ミルセン

α-ピネン 98%

Sigma-Aldrich

147524

α-ピネン

α-テルピネン analytical standard

Supelco

95652

α-テルピネン

Sabinene phyproof® Reference Substance

PHL82342

Sabinene

β-Pinene phyproof® Reference Substance

PHL89335

β-Pinene

David F Lima et al.
The Journal of pharmacy and pharmacology, 64(2), 283-292 (2012-01-10)
The aim of this work was to investigate the antinociceptive property of α-phellandrene (α-PHE) in experimental nociception models and possible mechanisms involved. Mass spectrometry was used to evaluate the purity and molecular mass of α-PHE. Macrophages from mice peritoneal cavity
Gökalp İşcan et al.
Chemistry & biodiversity, 9(8), 1525-1532 (2012-08-18)
Terpene derivatives converted by microbial biotransformation constitute an important resource for natural pharmaceutical, fragrance, and aroma substances. In the present study, the monoterpene α-phellandrene was biotransformed by 16 different strains of microorganisms (bacteria, fungi, and yeasts). The transformation metabolites were
Huai-sheng Hu et al.
Zhong yao cai = Zhongyaocai = Journal of Chinese medicinal materials, 32(1), 67-70 (2009-05-19)
The chemical constituents and antimicrobial activity of the essential oil from Acanthopanax brachypus were studied. The essential oil was extracted from the stem of A. brachypus by steam distillation, and its antimicrobial activity was tested in vitro. The chemical constituents
S Foss et al.
Systematic and applied microbiology, 21(2), 237-244 (1998-08-15)
Four pseudomonad strains 51Men, 54Pin, 62Car and 65Phen were recently isolated on the monoterpenes (+)-menthene, alpha-pinene, 2-carene and alpha-phellandrene as sole carbon source and nitrate as electron acceptor. These bacteria were characterised. The motile, mesophilic, Gram-negative rods had a strictly
Kazuhiro Okamoto et al.
Organic letters, 10(19), 4387-4389 (2008-09-06)
Chiral dienes possessing the bicyclo[2.2.2]octadiene framework were prepared readily through the [4 + 2] cycloaddition of ( R)-alpha-phellandrene with methyl propiolate as the key step. Diene 9, substituted with a tertiary alcohol on one of the two double bonds, is

プロトコル

-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

-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

GC Analysis of Sweet Orange Essential Oil on SLB®-5ms (10 m x 0.10 mm I.D., 0.10 μm), Fast GC Analysis

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