62862

Sigma-Aldrich

Sodium dodecyl sulfate

≥90%

Sinônimo(s):
Lauryl sulfate sodium salt, Sodium lauryl sulfate, Dodecyl sulfate sodium salt, SDS, Dodecyl sodium sulfate
Fórmula linear:
CH3(CH2)11OSO3Na
Número CAS:
Peso molecular:
288.38
Beilstein/REAXYS Number:
3599286
Número EC:
Número MDL:
eCl@ss:
39093306
ID de substância PubChem:
NACRES:
NA.21

Nível de qualidade

100

descrição

anionic
62

teor

≥90%

peso molecular

288.38 g/mol

aplicação(ões)

LC/MS: suitable
electrophoresis: suitable
protein quantification: suitable

pf

204-207 °C (lit.)

solubilidade

water: soluble

HLB

40

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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Categorias relacionadas

Aplicação

Anionic detergent

Pictogramas

CorrosionExclamation mark

Palavra indicadora

Danger

hazcat

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

storage_class_code

11 - Combustible Solids

WGK Alemanha

WGK 2

Ponto de fulgor (ºF)

338.0 °F

Ponto de fulgor (ºC)

170 °C

Equipamento de proteção individual

Eyeshields, Faceshields, Gloves, type P1 (EN143) respirator filter, type P3 (EN 143) respirator cartridges

Certificado de análise

Certificado de origem

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...
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)...
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...
Lekun Fang et al.
Oncotarget, 5(10), 2974-2987 (2014-06-11)
Colorectal cancer (CRC) is one of the most common cancers worldwide, especially in Western countries. Although chemotherapy is used as an adjuvant or as a palliative treatment, drug resistance poses a great challenge. This study intended to identify biomarkers as...
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...

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