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Documentos

71717

Sigma-Aldrich

Dodecilsulfatosódico

tested according to NF, mixture of sodium alkyl sulfates consisting mainly of sodium dodecyl sulfate

Sinónimos:

Dodecil sulfato de sodio, Dodecil sulfato sodium salt, Lauril sulfato sodium salt, Laurilsulfato de sodio, SDS

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About This Item

Fórmula lineal:
CH3(CH2)11OSO3Na
Número de CAS:
151-21-3
Peso molecular:
288.38
Beilstein/REAXYS Number:
3599286
EC Number:
205-788-1
MDL number:
MFCD00036175
UNSPSC Code:
12161900
eCl@ss:
39093306
PubChem Substance ID:
57652342
NACRES:
NA.21

agency

USP
tested according to NF

Quality Level

200

description

anionic
 62

assay

≥85.0% (content of sodium alkyl sulfates)

form

rod

mol wt

288.38 g/mol

mp

204-207 °C (lit.)

solubility

water: soluble

HLB

40

application(s)

pharmaceutical (small molecule)

SMILES string

[Na+].CCCCCCCCCCCCOS([O-])(=O)=O

InChI

1S/C12H26O4S.Na/c1-2-3-4-5-6-7-8-9-10-11-12-16-17(13,14)15;/h2-12H2,1H3,(H,13,14,15);/q;+1/p-1

InChI key

DBMJMQXJHONAFJ-UHFFFAOYSA-M

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Application

Detergente aniónico.

pictograms

CorrosionExclamation mark
GHS05,GHS07

signalword

Danger

Hazard Classifications

Acute Tox. 4 Oral - Aquatic Chronic 3 - Eye Dam. 1 - Skin Irrit. 2

Storage Class

11 - Combustible Solids

wgk_germany

WGK 2

flash_point_f

338.0 °F

flash_point_c

170 °C

ppe

Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges

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A M Maillard et al.
Molecular psychiatry, 20(1), 140-147 (2014-11-26)
Anatomical structures and mechanisms linking genes to neuropsychiatric disorders are not deciphered. Reciprocal copy number variants at the 16p11.2 BP4-BP5 locus offer a unique opportunity to study the intermediate phenotypes in carriers at high risk for autism spectrum disorder (ASD)
Shane Stegeman et al.
Cancer discovery, 5(4), 368-379 (2015-02-19)
Prostate cancer is the second most common malignancy among men worldwide. Genome-wide association studies have identified 100 risk variants for prostate cancer, which can explain approximately 33% of the familial risk of the disease. We hypothesized that a comprehensive analysis
S Desrivières et al.
Molecular psychiatry, 20(2), 263-274 (2014-02-12)
Despite the recognition that cortical thickness is heritable and correlates with intellectual ability in children and adolescents, the genes contributing to individual differences in these traits remain unknown. We conducted a large-scale association study in 1583 adolescents to identify genes
Susanne Kohl et al.
Nature genetics, 47(7), 757-765 (2015-06-02)
Achromatopsia (ACHM) is an autosomal recessive disorder characterized by color blindness, photophobia, nystagmus and severely reduced visual acuity. Using homozygosity mapping and whole-exome and candidate gene sequencing, we identified ten families carrying six homozygous and two compound-heterozygous mutations in the
Yan Xiang et al.
The Journal of clinical investigation, 125(6), 2293-2306 (2015-04-29)
Glutaminase (GLS), which converts glutamine to glutamate, plays a key role in cancer cell metabolism, growth, and proliferation. GLS is being explored as a cancer therapeutic target, but whether GLS inhibitors affect cancer cell-autonomous growth or the host microenvironment or
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