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171034

Sigma-Aldrich

tert-Nonyl mercaptan, mixture of isomers

≥97%

Synonym(s):

tert-Nonanethiol

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100 MG
143,00 $
1 G
262,00 $
5 G
743,00 $

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100 MG
143,00 $
1 G
262,00 $
5 G
743,00 $

About This Item

Empirical Formula (Hill Notation):
C9H20S
CAS Number:
Molecular Weight:
160.32
EC Number:
MDL number:
UNSPSC Code:
12162002
PubChem Substance ID:
NACRES:
NA.23

143,00 $


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Assay

≥97%

refractive index

n20/D 1.457 (lit.)

bp

188 °C (lit.)

density

0.856 g/mL at 25 °C (lit.)

SMILES string

CCCCCCC(C)(C)S

InChI

1S/C9H20S/c1-4-5-6-7-8-9(2,3)10/h10H,4-8H2,1-3H3

InChI key

MPBLPZLNKKGCGP-UHFFFAOYSA-N

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This Item
364622456292364630
isotopic purity

98 atom % D

isotopic purity

98 atom % D

isotopic purity

98 atom % D

isotopic purity

98 atom % D

mass shift

M+10

mass shift

M+10

mass shift

M+10

mass shift

M+14

Quality Level

200

Quality Level

200

Quality Level

200

Quality Level

200

form

solid

form

solid

form

solid

form

solid

mp

210-215 °C (lit.)

mp

98-100 °C (lit.)

mp

110-113 °C (lit.)

mp

212-213 °C (lit.)

bp

340 °C (lit.)

bp

340 °C (lit.)

bp

384 °C (lit.)

bp

-

Legal Information

Product of Arkema Inc.

Pictograms

FlameExclamation mark

Signal Word

Warning

Hazard Statements

Hazard Classifications

Eye Irrit. 2 - Flam. Liq. 3 - Skin Sens. 1 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

3 - Flammable liquids

WGK

WGK 3

Flash Point(F)

104.0 °F - closed cup

Flash Point(C)

40 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Katharina Neudorfer et al.
Diagnostic microbiology and infectious disease, 90(1), 58-63 (2017-12-03)
We tested the in vitro activity of dalbavancin, vancomycin and daptomycin against 83 enterococcal isolates in planktonic and biofilm states. The MIC90 for vancomycin-susceptible Enterococcus faecalis was 0.125 and 4μg/mL for dalbavancin and daptomycin, respectively. For vancomycin-resistant Enterococcus faecium, the
Helio S Sader et al.
Antimicrobial agents and chemotherapy, 62(3) (2017-12-22)
Dalbavancin activity was assessed against a large collection of Staphylococcus aureus isolates (n = 59,903), including isolates with decreased susceptibility to vancomycin (MIC, ≥2 mg/liter; n = 1,141), daptomycin (MIC, ≥2 mg/liter; n = 48), telavancin (MIC, ≥0.12 mg/liter; n
Zongru Guo
Acta pharmaceutica Sinica. B, 7(2), 119-136 (2017-03-18)
Drug innovation is characterized by painstaking molecular-level syntheses and modifications as the basic components of research and development. Similarly, natural products are chemically tailored and modified based upon their structural and biological properties. To some extent, the modification of natural
Michael A Pfaller et al.
International journal of antimicrobial agents, 51(4), 608-611 (2017-12-27)
Osteomyelitis is a difficult-to-treat infection that regularly involves prolonged use of systemic antibiotics. Dalbavancin has demonstrated activity against Gram-positive isolates, and has been considered as a candidate for the treatment of osteomyelitis in adults and children. This study evaluated the
Valentin Al Jalali et al.
Clinical pharmacokinetics, 57(7), 797-816 (2018-01-15)
Telavancin was discovered by modifying the chemical structure of vancomycin and belongs to the group of lipoglycopeptides. It employs its antimicrobial potential through two distinct mechanisms of action: inhibition of bacterial cell wall synthesis and induction of bacterial membrane depolarization

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