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Merck
CN

62122

Sigma-Aldrich

(R)-(+)-柠檬烯

greener alternative

technical, ~90% (sum of enantiomers, GC)

别名:

(+)-对薄荷-1,8-二烯, (+)-香芹烯, (R)-4-异丙烯基-1-甲基-1-环己烯

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关于此项目

经验公式（希尔记法）:
C10H16
CAS Number:
5989-27-5
分子量:
136.23
Beilstein:
2204754
EC 号:
227-813-5
MDL编号:
MFCD00062991
UNSPSC代码:
12352002
PubChem化学物质编号:
329759709
NACRES:
NA.22

主要文件

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蒸汽密度

4.7 (vs air)

质量水平

100

蒸汽压

<3 mmHg ( 14.4 °C)

等级

technical

方案

~90% (sum of enantiomers, GC)

表单

liquid

旋光性

[α]20/D +112±5°, c = 10% in ethanol

expl. lim.

6.1 %

环保替代产品特性

Waste Prevention
Safer Solvents and Auxiliaries
Use of Renewable Feedstocks
Learn more about the Principles of Green Chemistry.

sustainability

Greener Alternative Product

折射率

n20/D 1.473 (lit.)

沸点

176-177 °C (lit.)

溶解性

water: insoluble

密度

0.842 g/mL at 20 °C (lit.)

环保替代产品分类

Aligned,

储存温度

2-8°C

SMILES字符串

CC(=C)[C@@H]1CCC(C)=CC1

InChI

1S/C10H16/c1-8(2)10-6-4-9(3)5-7-10/h4,10H,1,5-7H2,2-3H3/t10-/m0/s1

InChI key

XMGQYMWWDOXHJM-JTQLQIEISA-N

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相关类别

一般描述

(R)-(+)-柠檬烯存在于柑橘类水果的果皮油中。它是技术产品和精细香料中最常用的香料。它是从莳萝属（印度莳萝）中提取的香精油的主要成分。外消旋柠檬烯通过指状青霉菌丝体，经过对映选择性和对映特异性转化为（R)-(+)-α-松油醇。研究了真菌对（R）-（+）-和（S）-（-）-柠檬烯的生物转化。
（R）-（+）-柠檬烯是柠檬烯的一种光学活性（R）形式。柠檬烯是一种10碳环己酮单萜。广泛应用于化妆品行业。

应用

（R）-（+）-柠檬烯已被用于研究柠檬烯对利什曼原虫的体外和体内作用。

警示用语：

Danger

危险分类

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

储存分类代码

3 - Flammable liquids

WGK

WGK 2

闪点(°F)

123.8 °F - closed cup

闪点(°C)

51 °C - closed cup

个人防护装备

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

法规信息

危险化学品

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number
BCCF2454
BCBZ1768
BCBR2678V

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Bioconversion of (R)-(+)-limonene by P. digitatum (NRRL 1202)
Tan Q, et al.
Process. Biochem., 33(1), 29-37 (1998)
J C Demyttenaere et al.
Phytochemistry, 57(2), 199-208 (2001-05-31)
The biotransformation of (R)-(-)- and (S)-(-)-limonene by fungi was investigated. More than 60 fungal cultures were screened for their ability to bioconvert the substrate, using solid phase microextraction as the monitoring technique. After screening, the best fungal strains were selected
Antimicrobial activity profiles of the two enantiomers of limonene and carvone isolated from the oils of Mentha spicata and Anethum sowa.
Aggarwal KK, et al.
Flavour and Fragrance Journal, 17(1), 59-63 (2002)
Cedric S Graebin et al.
European journal of medicinal chemistry, 45(4), 1524-1528 (2010-02-02)
The synthesis and in vitro activity of R(+)-Limonene derivatives against Leishmania and Trypanosoma cruzi strains are reported. Seven compounds have shown better in vitro activity against Leishmania (V.)braziliensis than the standard drug pentamidine. Additionally, we have identified two promising new
W G Flamm et al.
Regulatory toxicology and pharmacology : RTP, 13(1), 70-86 (1991-02-01)
The monoterpene d-limonene is a naturally occurring chemical which is the major component in oil of orange. Currently, d-limonene is widely used as a flavor and fragrance and is listed to be generally recognized as safe (GRAS) in food by
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Chromatograms

suitable for GC

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