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Merck
모든 사진(1)

주요 문서

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422754

Sigma-Aldrich

3-Decyn-1-ol

97%

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모든 사진(1)

About This Item

Linear Formula:
CH3(CH2)5C≡CCH2CH2OH
CAS Number:
51721-39-2
Molecular Weight:
154.25
MDL number:
MFCD00040917
UNSPSC 코드:
12352100
PubChem Substance ID:
24866451
NACRES:
NA.22

분석

97%

양식

liquid

refractive index

n20/D 1.459 (lit.)

bp

130-131 °C/22 mmHg (lit.)

density

0.877 g/mL at 25 °C (lit.)

작용기

hydroxyl

SMILES string

CCCCCCC#CCCO

InChI

1S/C10H18O/c1-2-3-4-5-6-7-8-9-10-11/h11H,2-6,9-10H2,1H3

InChI key

YGEQBZUDPQQIFI-UHFFFAOYSA-N

일반 설명

3-Decyn-1-ol is primary homo-propargylic alcohol derivative.[1] It has been reported to be formed during the isomerization of 2-decyn-1-ol in the presence of sodium salt of 1,3-diaminopropane.[2] Its toxicity has been evaluated on the green alga, Pseudokirchneriella subcapitata in terms of EC50 (median effective concentration) and NOEC (no observed effect level) values.[1] It undergoes semi hydrogenation in the presence of Lindlar catalyst to form cis-3-decen-1-ol.[3]

애플리케이션

3-Decyn-1-ol may be used in the following studies:
  • As a starting material in the synthesis of 3′-deoxyribolactones.[4]
  • As a starting material in the synthesis of (Z)-3-decen-1-ol by hydrogenation over P-2 nickel.[5]
  • As a reagent in the synthesis of methyl 9-decynoate.[6]

픽토그램

Exclamation mark
GHS07

신호어

Warning

유해 및 위험 성명서

H315,H319,H335

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

표적 기관

Respiratory system

Storage Class Code

10 - Combustible liquids

WGK

WGK 3

Flash Point (°F)

224.6 °F - closed cup

Flash Point (°C)

107 °C - closed cup

개인 보호 장비

Eyeshields, Gloves, type ABEK (EN14387) respirator filter

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시험 성적서(COA)

Lot/Batch Number
MKCL1044
MKCK5218
MKCK4976
MKCF7726
MKCD4434

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문서 라이브러리에서 최근에 구매한 제품에 대한 문서를 찾아보세요.

문서 라이브러리 방문

The rearrangement of isomeric linear decyn-1-ols by reaction with the sodium salt of 1, 3-diaminopropane.
Macaulay SR.
Canadian Journal of Chemistry, 58(23), 2567-2572 (1980)
Seiji Itoh et al.
Bioscience, biotechnology, and biochemistry, 66(7), 1591-1596 (2002-09-13)
Both the (17R)- and (17S)-isomers of volicitin, which is contained in the oral secretion of the beet armyworm and induces corn seedlings to emit a blend of volatile compounds to attract the natural enemy of the herbivore, were synthesized via
Synthesis of 3'-Deoxyribolactones using a Hydrolysis-Induced Lactonization Cascade Reaction of Epoxy Cyanohydrins.
Vugts DJ, et al.
European Journal of Organic Chemistry, 2008(8), 1336-1339 (2008)
Miriam F Cooperband et al.
Journal of chemical ecology, 38(1), 52-62 (2012-01-17)
A male-produced pheromone that attracts both males and females was identified for the European woodwasp, Sirex noctilio, a serious pest of pine trees. Males displayed excitatory behaviors when placed in groups, and were attracted to the odors from males that
Chung Yuan Chen et al.
Journal of environmental monitoring : JEM, 14(1), 181-186 (2011-11-23)
The present study evaluates the toxicity of 34 propargylic alcohols, including primary, primary homo-, secondary, and tertiary alcohols, based on their effects on phytoplankton. A closed-system algal toxicity test was applied because the closed-system technique presents more realistic concentration-response relationships
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