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431362

Sigma-Aldrich

Hidroxilamina

99.999% trace metals basis

Sinônimo(s):

Cloreto de hidroxilamônio

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About This Item

Fórmula linear:
NH2OH · HCl
Número CAS:
5470-11-1
Peso molecular:
69.49
Beilstein:
3539763
Número CE:
226-798-2
Número MDL:
MFCD00051089
Código UNSPSC:
12352301
ID de substância PubChem:
24867012
NACRES:
NA.22

grau

ACS reagent (specifications)

Ensaio

99.999% trace metals basis

Formulário

crystals

Impurezas

≤0.005% S compounds
≤0.25 meq/g Titr. free acid
<10 ppm total metallic impurities

resíduo de ignição

≤0.05%

pH

2.5-3.5 (20 °C, 50 g/L)

pf

155-157 °C (dec.) (lit.)

densidade

1.67 g/mL at 25 °C (lit.)

traços de cátion

Fe: ≤5 ppm
NH4+:, passes test
heavy metals: ≤5 ppm

cadeia de caracteres SMILES

Cl.NO

InChI

1S/ClH.H3NO/c;1-2/h1H;2H,1H2

chave InChI

WTDHULULXKLSOZ-UHFFFAOYSA-N

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Aplicação

Reactant for preparation of:
  • Organosilane amines as potent inhibitors and structural probes of influenza A virus M2 proton channel
  • Lamellarin D analogues as inibitors of topoisomerase I and potential antitumor agents
  • Azapeptide tocolytic agents as inhibitors of prostaglandin F2a receptor for preventing preterm labor
  • Thiazolidinones spiro-fused to indolin-2-ones as potent and selective inhibitors of Mycobacterium tuberculosis protein tyrosine phosphatase B
  • Orally bioavailable quinoline-based antidiabetic dipeptidyl peptidase IV inhibitors targeting Lys554
  • Pyrimidine nucleoside derivatives with nitric oxide donors as antiviral agents
  • Benzyladenosine compounds targeting adenosine A2A receptor and adenosine transporter for neuroprotection
  • Naphthol derivatives as inhibitors of the vanilloid receptor TRPV1 with improved potency in rat cystometry models of urinary incontinence

Ações bioquímicas/fisiológicas

Inibidor da MAO; inibe a agregação de plaquetas.

Características e benefícios

Meets A.C.S. reagent specifications.

Palavra indicadora

Warning

Classificações de perigo

Acute Tox. 4 Dermal - Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 2 - Carc. 2 - Eye Irrit. 2 - Met. Corr. 1 - Skin Irrit. 2 - Skin Sens. 1 - STOT RE 2 Oral

Órgãos-alvo

spleen

Código de classe de armazenamento

4.1A - Other explosive hazardous materials

Classe de risco de água (WGK)

WGK 3

Ponto de fulgor (°F)

Not applicable

Ponto de fulgor (°C)

Not applicable

Equipamento de proteção individual

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

Escolha uma das versões mais recentes:

Certificados de análise (COA)

Lot/Batch Number
MKCM6407
MKCJ7604
MKCF4222
MKCF1217
MKCB0034V

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Sigma-Aldrich

K2755

2-Keto-3-deoxyoctonate ammonium salt

Carine B Bourguet et al.
Journal of medicinal chemistry, 54(17), 6085-6097 (2011-07-22)
The prostaglandin-F2α (PGF2α) receptor (FP) was targeted to develop tocolytic agents for inhibiting preterm labor. Azabicycloalkane and azapeptide mimics 2-10 were synthesized based on the (3S,6S,9S)-indolizidin-2-one amino acid analogue PDC113.824 (1), which was shown to modulate FP by a biased
Salvatore Cananzi et al.
Bioorganic & medicinal chemistry, 19(16), 4971-4984 (2011-07-26)
A novel 5-oxa-6a,8-diazaindeno[2,1-b]phenanthren-7-one scaffold was designed and synthesized as an active analogue of the cytotoxic marine alkaloid Lamellarin D. The design was based on molecular modeling of the site of interaction of Lamellarin D with DNA-topoisomerase I cleavable complex, whereas
Jun Wang et al.
Journal of the American Chemical Society, 133(35), 13844-13847 (2011-08-09)
We describe the use of organosilanes as inhibitors and structural probes of a membrane protein, the M2 proton channel from influenza A virus. Organosilane amine inhibitors were found to be generally as potent as their carbon analogues in targeting WT
Hironobu Maezaki et al.
Bioorganic & medicinal chemistry, 19(15), 4482-4498 (2011-07-12)
Dipeptidyl peptidase IV (DPP-4) inhibition is a validated therapeutic option for type 2 diabetes, exhibiting multiple antidiabetic effects with little or no risk of hypoglycemia. In our studies involving non-covalent DPP-4 inhibitors, a novel series of quinoline-based inhibitors were designed
Shi, J.; et al.
Chinese Chemical Letters = Zhongguo Hua Xue Kuai Bao, 22, 899-899 (2011)
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