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545449

Sigma-Aldrich

5-Decyne

98%

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About This Item

Linear Formula:
CH3(CH2)3C≡C(CH2)3CH3
CAS Number:
1942-46-7
Molecular Weight:
138.25
MDL number:
MFCD00027277
UNSPSC Code:
12352100
PubChem Substance ID:
24878826
NACRES:
NA.22

Assay

98%

refractive index

n20/D 1.4340 (lit.)

density

0.766 g/mL at 25 °C (lit.)

SMILES string

CCCCC#CCCCC

InChI

1S/C10H18/c1-3-5-7-9-10-8-6-4-2/h3-8H2,1-2H3

InChI key

JWBQJUFCNOLNNC-UHFFFAOYSA-N

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General description

5-Decyne is a symmetrical dialkylacetylene derivative that can be prepared from 1-hexyne.

Application

5-Decyne may be used in the preparation of:
  • B

  • -(cis-5-decenyl)-9-BBN (9-BBN= 9-borabicyclo[3,3,1]nonane)
  • 5-decanone
  • (Z)-5-ethyl-6-decene
  • trans-5-decene

Pictograms

FlameCorrosion
GHS02,GHS05

Signal Word

Danger

Hazard Statements

H226,H314

Hazard Classifications

Eye Dam. 1 - Flam. Liq. 3 - Skin Corr. 1B

Storage Class Code

3 - Flammable liquids

WGK

WGK 3

Flash Point(F)

136.4 °F - closed cup

Flash Point(C)

58 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

FSL

Group 4: Flammable liquids
Type 2 petroleums
Hazardous rank III
Water insoluble liquid

JAN Code

545449-25G:
545449-BULK:
545449-VAR:

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Xi Z, et al.
The Journal of Organic Chemistry, 60(14), 4444-4448 (1995)
Reduction of organic compounds by lithium in low molecular weight amines. II. Stereochemistry. Chemical reduction of an isolated non-terminal double bond.
Benkeser RA, et al.
Journal of the American Chemical Society, 77(12), 3378-3379 (1955)
Hydroboration. 50. Hydroboration of representative alkynes with 9-borabicyclo [3.3.1] nonane-a simple synthesis of versatile vinyl bora and gem-dibora intermediates.
Brown HC, et al.
Journal of the American Chemical Society, 101(1), 96-99 (1979)
Structure-activity relationships in the destruction of cytochrome P-450 mediated by certain ethynyl-substituted compounds in rats.
I N White
Biochemical pharmacology, 29(24), 3253-3255 (1980-12-01)

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