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Merck
CN

W261505

Sigma-Aldrich

月桂醛

≥95%, stabilized, FCC, FG

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别名:
十二醛, 1-十二醛, 十二烷醛, 樟醛
线性分子式:
CH3(CH2)10CHO
CAS号:
分子量:
184.32
FEMA编号:
2615
Beilstein:
1703917
EC 号:
欧洲委员会编号:
99
MDL编号:
UNSPSC代码:
12164502
PubChem化学物质编号:
Flavis编号:
5.011
NACRES:
NA.21

生物来源

synthetic

质量水平

等级

FG
Fragrance grade
Halal
Kosher

Agency

follows IFRA guidelines
meets purity specifications of JECFA

管理合规性

EU Regulation 1223/2009
EU Regulation 1334/2008 & 178/2002
FCC
FDA 21 CFR 117
FDA 21 CFR 172.515

检测方案

≥95%

包含

α-tocopherol as stabilizer

折射率

n20/D 1.435 (lit.)

bp

185 °C/100 mmHg (lit.)

密度

0.831 g/mL at 25 °C (lit.)

应用

flavors and fragrances

文件

see Safety & Documentation for available documents

食品过敏原

no known allergens

致敏芳香化合物

no known allergens

性状检查

green; citrus; waxy; floral; soapy

SMILES字符串

CCCCCCCCCCCC=O

InChI

1S/C12H24O/c1-2-3-4-5-6-7-8-9-10-11-12-13/h12H,2-11H2,1H3

InChI key

HFJRKMMYBMWEAD-UHFFFAOYSA-N

一般描述

Lauric aldehyde is one of the main aliphatic green volatile compounds in macerated grape cluster stems. It is also one of the key flavor constituents of grapefruit oil.

应用


  • Utility of ToxTracker in animal alternative testing strategy for fragrance materials.: This study highlights the use of ToxTracker, a suite of reporter cell lines, to evaluate the genetic toxicity of fragrance materials, including lauric aldehyde, offering a potential alternative to animal testing and advancing the safety assessment of consumer products (Thakkar et al., 2023).

  • In vitro evaluation of polymeric micelles based on hydrophobically-modified sulfated chitosan as a carrier of doxorubicin.: Research demonstrates the potential of hydrophobically-modified sulfated chitosan micelles, incorporating lauric aldehyde, for improving the delivery of chemotherapeutic agents, particularly doxorubicin, enhancing drug stability and reducing side effects (Wang et al., 2012).

  • Biocompatibility of injectable chitosan-phospholipid implant systems.: Investigates the biocompatibility of chitosan-phospholipid injectable implants, where lauric aldehyde could play a role in modifying polymer matrices to enhance biocompatibility and drug release profiles, critical for medical implant technologies (De Souza et al., 2009).


象形图

Exclamation markEnvironment

警示用语:

Warning

危险声明

危险分类

Aquatic Chronic 2 - Skin Irrit. 2

WGK

WGK 2

闪点(°F)

closed cup

闪点(°C)

closed cup

个人防护装备

Eyeshields, Gloves, type ABEK (EN14387) respirator filter


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Green odorants of grape cluster stem and their ability to cause a wine stemmy flavor.
Hashizume K & Samuta T.
Journal of Agricultural and Food Chemistry, 45(4), 1333-1337 (1997)
Analysis of carbonyl flavor constituents from grapefruit oil.
Moshonas MG.
Journal of Agricultural and Food Chemistry, 19(4), 769-770 (1971)
Markus A Keller et al.
Nature communications, 5, 4439-4439 (2014-07-23)
Mutations in the gene coding for membrane-bound fatty aldehyde dehydrogenase (FALDH) lead to toxic accumulation of lipid species and development of the Sjögren-Larsson Syndrome (SLS), a rare disorder characterized by skin defects and mental retardation. Here, we present the crystallographic
James Liu et al.
Journal of pharmaceutical sciences, 104(3), 1187-1196 (2015-01-13)
The objective of this study is to develop and compare several Sorafenib-loaded biocompatible nanoparticle models in order to optimize drug delivery and tumor cellular kill thereby improving the quality of Sorafenib-regimented chemotherapy. Sorafenib-loaded poly (lactic-co-glycolic) acid (PLGA), 1,2-dipalmitoyl-sn-glycero-3-phosphocholine (DPPC) liposomes
Pingxi Xu et al.
Proceedings of the National Academy of Sciences of the United States of America, 111(46), 16592-16597 (2014-10-29)
Insect repellents are important prophylactic tools for travelers and populations living in endemic areas of malaria, dengue, encephalitis, and other vector-borne diseases. DEET (N,N-diethyl-3-methylbenzamide) is a 6-decade-old synthetic repellent, which is still considered the gold standard of mosquito repellents. Mosquitoes

实验方案

-β-Farnesene; α-Huµlene; Germacrene D; (+)-Valencene; Bicyclogermacrene; (+)-δ-Cadinene

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