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Documenti

86040

Supelco

Acido sulfamico

analytical standard (for acidimetry), ACS reagent

Sinonimo/i:

Acido amidosolfonico

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About This Item

Formula condensata:
NH2SO3H
Numero CAS:
5329-14-6
Peso molecolare:
97.09
Numero CE:
226-218-8
Numero MDL:
MFCD00011603
Codice UNSPSC:
12161700
ID PubChem:
329769435
NACRES:
NA.25

Grado

ACS reagent
analytical standard (for acidimetry)

Livello qualitativo

100

agenzia

complies with DIN 19266

Saggio

99.3-100.3% (dried material)

Punto di fusione

215-225 °C (dec.) (lit.)

Anioni in tracce

chloride (Cl-): ≤10 mg/kg
sulfate (SO42-): ≤500 mg/kg

Cationi in tracce

Ca: ≤10 mg/kg
Cd: ≤5 mg/kg
Co: ≤5 mg/kg
Cr: ≤5 mg/kg
Cu: ≤5 mg/kg
Fe: ≤5 mg/kg
K: ≤50 mg/kg
Mg: ≤5 mg/kg
Mn: ≤5 mg/kg
Na: ≤50 mg/kg
Ni: ≤10 mg/kg
Pb: ≤5 mg/kg
Zn: ≤5 mg/kg

applicazioni

environmental
food and beverages
general analytical
industrial qc
pharmaceutical

Formato

mixture

Stringa SMILE

NS(O)(=O)=O

InChI

1S/H3NO3S/c1-5(2,3)4/h(H3,1,2,3,4)
IIACRCGMVDHOTQ-UHFFFAOYSA-N

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Categorie correlate

Descrizione generale

Sulfamic acid, a strong inorganic acid, exists in crystalline form. It is stable, non-hygroscopic, odorless, and colorless in dry state, making its commercial packaging and handling convenient.

Applicazioni

It can be used as an acidimetric standard for analytical applications.
Sulfamic acid also finds its use as a primary standard in non-aqueous visual, conductometric, and potentiometric titrations.

Caratteristiche e vantaggi

  • Available in a secure glass bottle to ensure its stability for the entire shelf life until opened.
  • High-quality offering accurate titer determinations
  • Accompanied by a detailed certificate of analysis (CoA)

Pittogrammi

Exclamation mark
GHS07

Avvertenze

Warning

Indicazioni di pericolo

H315,H319,H412

Classi di pericolo

Aquatic Chronic 3 - Eye Irrit. 2 - Skin Irrit. 2

Codice della classe di stoccaggio

8B - Non-combustible corrosive hazardous materials

Classe di pericolosità dell'acqua (WGK)

WGK 1

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable

Dispositivi di protezione individuale

dust mask type N95 (US), Eyeshields, Faceshields, Gloves

Choose from one of the most recent versions:

Certificati d'analisi (COA)

Lot/Batch Number
BCCG4172
BCCF2002
BCCC7172
BCCC0478
BCCB3235

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Targeting tumour associated carbonic anhydrase (CA, EC 4.2.1.1) isoforms IX and XII is now considered as a pertinent approach for the development of new cancer therapeutics against hypoxic tumours. In the last period, with the help of X-ray crystallography, much
Patricia Chávez et al.
The Journal of organic chemistry, 77(4), 1922-1930 (2012-01-31)
An intramolecular diamination of acrylates is reported using sulfamates as nitrogen sources. This reaction proceeds under palladium(II) catalysis with copper bromide as oxidant and gives rise to anti-configured 2,3-diamino carboxylates as bicyclic sulfamate derivatives. An aminobrominated intermediate within the diamination
Na Zhang et al.
The Journal of organic chemistry, 77(14), 5956-5964 (2012-06-21)
The efficiency of arylboron-based nucleophiles, boronic acid, potassium trifluoroborate, neopentylglycolboronate, and pinacol boronate in nickel-catalyzed Suzuki-Miyaura cross-coupling reactions with the two C-O electrophiles, mesylates, and sulfamates was compared. Arylboronic acid is the most reactive and most atom-economic of the four
Amit Saha et al.
Chemical communications (Cambridge, England), 48(71), 8889-8891 (2012-07-21)
Unnatural α-amino acids containing dithiocarbamate side chains were synthesized by a one-pot reaction of in situ generated dithiocarbamate anions with sulfamidates. A wide range of these anions participated in the highly regio- and stereo-selective ring opening of sulfamidates to produce
Derek J Langeslay et al.
Analytical chemistry, 83(20), 8006-8010 (2011-09-15)
Sulfamate (NHSO(3)(-)) groups are critically important structural elements of the glycosaminoglycans heparin and heparan sulfate (HS). Experimental conditions are presented for detection of the sulfamate (1)H NMR resonances in aqueous solution. NMR spectra reported for N-sulfoglucosamine (GlcNS) and the synthetic
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