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Merck

W304522

Sigma-Aldrich

(−)−α-松油醇

greener alternative

natural, ≥96%, FCC, FG

别名:

(S)-2-(4-三甲基-3-环己烯)-2-丙醇, (S)-对薄荷-1-烯-8-醇

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About This Item

经验公式(希尔记法):
C10H18O
CAS号:
分子量:
154.25
FEMA號碼:
3045
Beilstein:
2325137
EC號碼:
歐洲委員會號碼:
62c
MDL號碼:
分類程式碼代碼:
12164502
PubChem物質ID:
Flavis號碼:
2.014
NACRES:
NA.21
agency:
follows IFRA guidelines

等級

FG
Fragrance grade
Halal
Kosher
natural

品質等級

agency

follows IFRA guidelines

法律遵循

EU Regulation 1223/2009
EU Regulation 1334/2008 & 178/2002
FCC
FDA 21 CFR 172.515
FDA 21 CFR 178.1010

化驗

≥96%

環保替代產品特色

Less Hazardous Chemical Syntheses
Use of Renewable Feedstocks
Learn more about the Principles of Green Chemistry.

sustainability

Greener Alternative Product

折射率

n20/D 1482 (lit.)

bp

217-218 °C (lit.)

mp

31-35 °C (lit.)

密度

0.93 g/mL at 25 °C (lit.)

應用

flavors and fragrances

文件

see Safety & Documentation for available documents

食物過敏原

no known allergens

香料過敏原

α-terpineol

環保替代類別

感官的

lilac; citrus; woody; floral; pine

SMILES 字串

CC1=CC[C@@H](C(O)(C)C)CC1

InChI

1S/C10H18O/c1-8-4-6-9(7-5-8)10(2,3)11/h4,9,11H,5-7H2,1-3H3/t9-/m1/s1

InChI 密鑰

WUOACPNHFRMFPN-SECBINFHSA-N

一般說明

α-松油醇是一种单萜,主要存在于松树、迷迭香和茶树等植物的精油中。
α-萜品醇是一种单萜醇。它是互生叶白千层( Melaleuca alternifolia,茶树)精油的抗真菌成分之一。它还存在于牛至(Origanum)精油和迷迭香(Rosmarinus officinalis )精油中。
我们竭诚为您带来满足绿色替代产品四大类别要求的替代产品。本品为生物基产品,在“危险性较小的化学合成”和“使用可再生原料”绿色化学原则方面取得了重大进步。

應用

酯类α松油醇的酯类化合物特有薰衣草、香柠檬香气,广泛用于烘焙食品、冷冻奶制品、口香糖、酒精和非酒精饮料、肉制品。

象形圖

Corrosion

訊號詞

Danger

危險聲明

危險分類

Eye Dam. 1 - Skin Irrit. 2

儲存類別代碼

11 - Combustible Solids

水污染物質分類(WGK)

WGK 2

閃點(°F)

204.8 °F - closed cup

閃點(°C)

96 °C - closed cup

個人防護裝備

dust mask type N95 (US), Eyeshields, Gloves


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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访问文档库

Plant essential oils for pest and disease management.
Isman MB.
Crop Protection, 19(8), 603-608 (2000)
Comparative toxicity of Rosmarinus officinalis L. essential oil and blends of its major constituents against Tetranychus urticae Koch (Acari: Tetranychidae) on two different host plants.
Miresmailli S, et al.
Pest Management Science, 62(4), 366-371 (2006)
Antimicrobial testings and gas chromatographic analysis of pure oxygenated monoterpenes 1, 8-cineole, ?-terpineol, terpinen-4-ol and camphor as well as target compounds in essential oils of pine (Pinus pinaster), rosemary (Rosmarinus officinalis), tea tree (Melaleuca alternifolia).
Jirovetz L, et al.
Scientia Pharmaceutica, 73(1), 27-38 (2005)
Antimicrobial and cytotoxic activities of Origanum essential oils.
Sivropoulou A, et al.
Journal of Agricultural and Food Chemistry, 44(5), 1202-1205 (1996)
Acute, sublethal, antifeedant, and synergistic effects of monoterpenoid essential oil compounds on the tobacco cutworm, Spodoptera litura (Lep., Noctuidae).
Hummelbrunner LA & Isman MB.
Journal of Agricultural and Food Chemistry, 49(2), 715-720 (2001)

实验方案

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

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

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

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