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제품정보 (DICE 배송 시 비용 별도)
Linear Formula:
CH3(CH2)10CON(CH3)CH2COONa
CAS 번호:
Molecular Weight:
293.38
UNSPSC Code:
12161902
NACRES:
NA.25
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
5322974
description
anionic
Quality Level
assay
≥97.0% (HPLC)
form
liquid
quality
30% aqueous solution
mol wt
average mol wt 600
aggregation number
2
technique(s)
protein quantification: suitable
pH
7.0-9.0 (25 °C)
CMC
14.6
solubility
water: soluble at 20 °C (soluble)
density
1.033 g/mL at 20 °C
cation traces
Ca: ≤20 mg/kg, Cd: ≤5 mg/kg, Co: ≤5 mg/kg, Cr: ≤5 mg/kg, Cu: ≤5 mg/kg, Fe: ≤10 mg/kg, K: ≤70 mg/kg, Mg: ≤10 mg/kg, Mn: ≤5 mg/kg, Ni: ≤5 mg/kg, Pb: ≤5 mg/kg, Zn: ≤5 mg/kg
SMILES string
[Na+].CCCCCCCCCCCC(=O)N(C)CC([O-])=O
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
InChI key
KSAVQLQVUXSOCR-UHFFFAOYSA-M
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Application
N-Lauroylsarcosine (Sarcosyl) is an ionic surfactant useful in a wide range of solubilization and permeation applications from solubilization of membrane proteins to enhancement of skin permeability in transdermal applications.
Other Notes
Solubilization of membrane proteins; useful for rupturing of eukaryote cells in transcription studies; In the lysis of Clostridium perfringens for rapid extraction of plasmids
ppe
Eyeshields, Gloves
wgk
WGK 1
signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Inhalation - Eye Irrit. 2
저장 등급
10 - Combustible liquids
H Wroblewski et al.
Biochimie, 60(4), 389-398 (1978-01-01)
1. Up to 90 per cent of the membrane proteins from Spiroplasma citri could be solubilized with the anionic detergent Sarkosyl (sodium lauroyl-sarcosinate). Maximal solubilization was obtained with 6 to 20 mumoles of of detergent per mg of membrane protein.
Properties of the polyoma virus transcription complex obtained from mouse nuclei.
R J Shmookler et al.
Virology, 57(1), 122-127 (1974-01-01)
D E Mahony et al.
Applied and environmental microbiology, 51(3), 521-523 (1986-03-01)
Two rapid methods were evaluated for their extraction of plasmids from Clostridium perfringens. The first method involved lysis of 1 to 2 ml of C. perfringens culture by treatment with hyaluronidase, lysozyme, and sarcosyl. DNA, extracted with phenol-chloroform, was treated
P. Gariglio et al.
Febs Letters, 44, 430-430 (1974)
Rhonda I Hobb et al.
Microbiology (Reading, England), 155(Pt 3), 979-988 (2009-02-28)
Although infection with Campylobacter jejuni is one of the leading causes of gastroenteritis worldwide, relatively little is known about the factors that are required to elicit a protective immune response. The need for a vaccine against this pathogen is well
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