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Key Documents

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177482

Sigma-Aldrich

1,16-Hexadecanediol

97%

Synonym(s):

Hexadecamethylene glycol

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1 PKG
CN¥5,586.77

CN¥5,586.77

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1 PKG
CN¥5,586.77

About This Item

Linear Formula:
HO(CH2)16OH
CAS Number:
7735-42-4
Molecular Weight:
258.44
Beilstein:
1811931
EC Number:
231-794-9
MDL number:
MFCD00002821
UNSPSC Code:
12352100
PubChem Substance ID:
24850640
NACRES:
NA.22

CN¥5,586.77

Please contact Customer Service for Availability
Request a Bulk Order

Quality Level

100

Assay

97%

form

solid

bp

197-199 °C/3 mmHg (lit.)

mp

91-94 °C (lit.)

functional group

hydroxyl

SMILES string

OCCCCCCCCCCCCCCCCO

InChI

1S/C16H34O2/c17-15-13-11-9-7-5-3-1-2-4-6-8-10-12-14-16-18/h17-18H,1-16H2

InChI key

GJBXIPOYHVMPQJ-UHFFFAOYSA-N

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K08670643K08670661K08670651
Kromasil® C18 HPLC Column 5 μm particle size, pore size 100 Å, L × I.D. 250 mm × 4.6 mm

K08670357

Kromasil® C18 HPLC Column

vibrant-m

K08670643

Kromasil® C18 HPLC Column

Kromasil® C18 HPLC Column 5 μm particle size, pore size 100 Å, L × I.D. 250 mm × 4 mm

K08670661

Kromasil® C18 HPLC Column

Kromasil® C18 HPLC Column 5 μm particle size, pore size 100 Å, L × I.D. 100 mm × 21.2 mm

K08670651

Kromasil® C18 HPLC Column

particle size

5 μm

particle size

3.5 μm

particle size

5 μm

particle size

5 μm

matrix active group

C18 (octadecyl) phase

matrix active group

C18 (octadecyl) phase

matrix active group

C18 (octadecyl) phase

matrix active group

C18 (octadecyl) phase

separation technique

reversed phase

separation technique

reversed phase

separation technique

reversed phase

separation technique

reversed phase

product line

Kromasil®

product line

Kromasil®

product line

Kromasil®

product line

Kromasil®

agency

suitable for USP L1

agency

suitable for USP L1

agency

suitable for USP L1

agency

suitable for USP L1

technique(s)

HPLC: suitable

technique(s)

HPLC: suitable

technique(s)

HPLC: suitable

technique(s)

HPLC: suitable

Application

1,16-Hexadecanediol was used to activate Mps1 MAP kinase pathway[1]. It was also used to accumulate BChl c monoesterified with the corresponding diols[2].

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H315

Hazard Classifications

Skin Irrit. 2

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves
  • Specification Sheet

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    Certificates of Analysis (COA)

    Lot/Batch Number
    SHBK2257
    02411TH
    00104JH
    14513DH
    02328JE

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    Misa Kuroki et al.
    Scientific reports, 7(1), 9697-9697 (2017-08-31)
    The rice blast fungus Magnaporthe oryzae differentiates a specialized infection structure called an appressorium to invade rice cells. In this report, we show that CBP1, which encodes a chitin-deacetylase, is involved in the induction phase of appressorium differentiation. We demonstrate
    Takashi Fujikawa et al.
    Molecular microbiology, 73(4), 553-570 (2009-07-16)
    Oligosaccharides derived from cell wall of fungal pathogens induce host primary immune responses. To understand fungal strategies circumventing the host plant immune responses, cell wall polysaccharide localization was investigated using fluorescent labels during infectious structure differentiation in the rice blast
    Risato Nishimori et al.
    Biochemistry, 50(36), 7756-7764 (2011-08-19)
    Unnatural bacteriochlorophyll (BChl) c derivatives possessing a hydroxy group at the terminus of a hydrocarbon chain at the 17-propionate were biosynthesized in the green sulfur photosynthetic bacterium Chlorobaculum tepidum. Addition of exogenous 1,8-octanediol, 1,12-dodecanediol, and 1,16-hexadecanediol in acetone to liquid
    Ying Li et al.
    mBio, 11(2) (2020-03-27)
    The appressoria that are generated by the rice blast fungus Magnaporthe oryzae in response to surface cues are important for successful colonization. Previous work showed that regulators of G-protein signaling (RGS) and RGS-like proteins play critical roles in appressorium formation.
    Martin Korn et al.
    PloS one, 10(5), e0125960-e0125960 (2015-05-21)
    We used insertional mutagenesis by Agrobacterium tumefaciens mediated transformation (ATMT) to isolate pathogenicity mutants of Colletotrichum higginsianum. From a collection of 7200 insertion mutants we isolated 75 mutants with reduced symptoms. 19 of these were affected in host penetration, while

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