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Dokumente

A16602

Sigma-Aldrich

DL-N-Acetylhomocystein-Thiolacton

98%

Synonym(e):

2-Acetamido-4-mercaptobuttersäure-γ-thiolacton

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About This Item

Empirische Formel (Hill-System):
C6H9NO2S
CAS-Nummer:
1195-16-0
Molekulargewicht:
159.21
EG-Nummer:
214-793-8
MDL-Nummer:
MFCD00005480
UNSPSC-Code:
12352100
PubChem Substanz-ID:
24890578
NACRES:
NA.22

Assay

98%

Form

powder

mp (Schmelzpunkt)

109-111 °C (lit.)

SMILES String

CC(=O)NC1CCSC1=O

InChI

1S/C6H9NO2S/c1-4(8)7-5-2-3-10-6(5)9/h5H,2-3H2,1H3,(H,7,8)

InChIKey

NRFJZTXWLKPZAV-UHFFFAOYSA-N

Anwendung

<ul>
<li><strong>Ultrasonic synthesis of stable oil filled microcapsules:</strong> This study explores the ultrasonic synthesis of oil-filled microcapsules using thiolated chitosan, potentially involving derivatives like N-Acetylhomocysteine thiolactone for improved stability and functional properties. The research provides insights into advanced microencapsulation techniques relevant in pharmaceutical and industrial applications (

Piktogramme

Skull and crossbones
GHS06

Signalwort

Danger

H-Sätze

H301

P-Sätze

P301 + P310

Gefahreneinstufungen

Acute Tox. 3 Oral

Lagerklassenschlüssel

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

WGK

WGK 3

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable

Persönliche Schutzausrüstung

Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges

Analysenzertifikate (COA)

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L-Homocystein &#8805;98.0% (NT)

Sigma-Aldrich

69453

L-Homocystein

tert-Butylglycidylether 99%

Sigma-Aldrich

251712

tert-Butylglycidylether

L-Homocystin &#8805;98% (HPLC)

Sigma-Aldrich

H6010

L-Homocystin

Bromacetylchlorid &#8805;95% (GC)

Sigma-Aldrich

16120

Bromacetylchlorid

N-Acetylcysteinamid &#8805;98% (HPLC)

Sigma-Aldrich

A0737

N-Acetylcysteinamid

I Flechner et al.
Diabetes research (Edinburgh, Scotland), 13(2), 67-73 (1990-02-01)
The possible value of radical scavengers in the prevention of beta cell destruction was studied in two animal models of type I diabetes. Eight compounds were tested alone or in combinations. In the low-dose streptozotocin model treatment started 24 hr
Fixed drug eruption due to citiolone.
P G Delgado et al.
Contact dermatitis, 33(5), 352-352 (1995-11-01)
R W Powers et al.
Endocrinology, 137(7), 3101-3110 (1996-07-01)
The activity of nitric oxide (NO) has been implicated as an important mediator in ovarian function, including the regulation of the blood-follicle barrier and ovulation. Both clinical and experimental diabetes have been found to impair endothelial-dependent vascular activity through the
P P Sood et al.
Journal of environmental pathology, toxicology and oncology : official organ of the International Society for Environmental Toxicology and Cancer, 14(2), 101-105 (1995-01-01)
Male albino mice were intoxicated with a daily dose of 1 mg/kg of methylmercury chloride (MMC) for 7 days, and were treated thereafter with glutathione, N-acetyl-DL-homocysteine thiolactone, vitamin B complex, and vitamin E, either alone or in combinations, for the
[Serum sickness type reaction to citiolone].
M Luque Sánchez et al.
Atencion primaria, 16(5), 295-296 (1995-09-30)
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