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192422

Sigma-Aldrich

1-Bromotridecane

98%

Synonym(s):

Tridecyl bromide

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About This Item

Linear Formula:
CH3(CH2)12Br
CAS Number:
765-09-3
Molecular Weight:
263.26
Beilstein:
1739992
EC Number:
212-138-0
MDL number:
MFCD00000227
UNSPSC Code:
12352100
PubChem Substance ID:
24851548
NACRES:
NA.22
form:
liquid
Assay:
98%

vapor density

9.2 (vs air)

Quality Level

200

Assay

98%

form

liquid

refractive index

n20/D 1.459 (lit.)

bp

148-150 °C/10 mmHg (lit.)

mp

4-7 °C (lit.)

density

1.03 g/mL at 25 °C (lit.)

functional group

alkyl halide
bromo

SMILES string

CCCCCCCCCCCCCBr

InChI

1S/C13H27Br/c1-2-3-4-5-6-7-8-9-10-11-12-13-14/h2-13H2,1H3

InChI key

BFDNZQUBFCYTIC-UHFFFAOYSA-N

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Related Categories

Application

1-Bromotridecane was used in the synthesis of:
  • tetradecanoic acid enriched with 13C at carbons 1, 3, or 6
  • (Z)-7-henicosene
  • (Z)-(2′R)-[N-carboethoxypyrrolidine]tetradec-1-ene
  • 2,3,6,7,10,11,14,15-octaalkyloxytetrabenzo[a,d,g,jlcyclododecatetraenes (CTTV-n) containing n=4-15 methylenic units in the alkyloxy substituents

Storage Class Code

10 - Combustible liquids

WGK

WGK 3

Flash Point(F)

>230.0 °F - closed cup

Flash Point(C)

> 110 °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 3 petroleums
Hazardous rank III
Water insoluble liquid

JAN Code

192422-BULK:
192422-VAR:
192422-5G:
192422-100G:
192422-25G:

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Certificates of Analysis (COA)

Lot/Batch Number
BCCJ8871
BCCG0231
BCCD8048
BCCD5061
BCCD7590

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B V Burger et al.
Journal of chemical ecology, 30(8), 1603-1611 (2004-11-13)
Using gas chromatography-mass spectrometry in conjunction with auxiliary techniques such as solid phase microextraction and determination of double bond positions by means of dimethyl disulfide derivatization, 45 constituents of the uropygial secretion of the green woodhoopoe, Phoeniculus purpureus, have been
Alkyloxy-substituted CTTV derivatives that exhibit columnar mesophases.
Percec V, et al.
Journal of Materials Chemistry, 1(2), 217-222 (1991)
J T Sparrow et al.
Journal of lipid research, 24(7), 938-941 (1983-07-01)
The synthesis of tetradecanoic acid enriched with 13C at carbons 1, 3, or 6 is described. The label at the carbonyl carbon was introduced by treating 1-bromotridecane with K13CN (90% enriched) to form the 13C-labeled nitrile, which upon hydrolysis yielded
A concise synthesis of (R)-Bgugaine, a pyrrolidine alkaloid from Arisarum vulgare.
Majik MS, et al.
J. Chem. Res. (M), 2008(3), 121-122 (2008)

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