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크기 선택
제품정보 (DICE 배송 시 비용 별도)
Linear Formula:
CH3(CH2)10CON(CH3)CH2COONa
CAS 번호:
Molecular Weight:
293.38
UNSPSC Code:
12352107
NACRES:
NA.32
PubChem Substance ID:
EC Number:
205-281-5
Beilstein/REAXYS Number:
5322974
MDL number:
InChI key
KSAVQLQVUXSOCR-UHFFFAOYSA-M
InChI
1S/C15H29NO3.Na/c1-3-4-5-6-7-8-9-10-11-12-14(17)16(2)13-15(18)19;/h3-13H2,1-2H3,(H,18,19);/q;+1/p-1
SMILES string
[Na+].CCCCCCCCCCCC(=O)N(C)CC([O-])=O
description
anionic
assay
≥94%
form
powder
mol wt
micellar avg mol wt 600, average mol wt 600
aggregation number
2
technique(s)
oligo synthesis: suitable
CMC
14.6 mM (20-25°C)
solubility
H2O: 100 mg/mL, clear to slightly hazy, colorless to faintly yellow
density
1,14 g/cm3 at 20 °C (1,14 g/cm3 at 20 °C)
Quality Level
유사한 제품을 찾으십니까? 방문 제품 비교 안내
Application
N-Lauroylsarcosine sodium salt has been used as one of the components of the lysing solution in the cornet assay. It has been used for lysing protoplasts in the process of chromosomal DNA isolation form Streptococcus mutans.
Biochem/physiol Actions
N-Lauroylsarcosine is an anionic surfactant which also has protein denaturant potency. In addition, it has been shown as a microbicide for sexually transmitted diseases.
Other Notes
Anionic surfactant.
signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 2 Inhalation - Eye Dam. 1 - Skin Irrit. 2
저장 등급
6.1B - Non-combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials
wgk
WGK 1
ppe
Eyeshields, Gloves, type N95 (US)
P W Caufield et al.
Journal of clinical microbiology, 27(2), 274-278 (1989-02-01)
Attempts to study the acquisition, transmission, and other aspects of the natural history of Streptococcus mutans infections in humans have been hampered by limitations and inconsistencies in methods by which phenotypic characteristics of individual isolates are examined. Because most mutans
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Genetics and molecular research : GMR, 7(4), 1414-1421 (2009-02-19)
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Frontiers in molecular neuroscience, 13, 106-106 (2020-08-09)
Alzheimer's disease (AD) is characterized by the accumulation in the brain of intraneuronal aggregates of abnormally and hyperphosphorylated tau proteins and of extracellular deposits of amyloid-β surrounded by dystrophic neurites. Numerous experimental models have shown that tau pathology develops in
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