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09699

Supelco

Ammonium carbamate

for decomposition

Synonym(s):

Carbamic acid ammonium salt

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About This Item

Linear Formula:
H2NCO2NH4
CAS Number:
1111-78-0
Molecular Weight:
78.07
Beilstein:
3914091
EC Number:
214-185-2
MDL number:
MFCD00013010
UNSPSC Code:
12000000
eCl@ss:
39033203
PubChem Substance ID:
329748802
NACRES:
NA.21

vapor pressure

100 mmHg ( 26.7 °C)

Quality Level

100

Assay

≥99.5% (T)

expl. lim.

2 %

ign. residue

≤0.002% (as SO4)

anion traces

chloride (Cl-): ≤5 mg/kg
nitrate (NO3-): ≤10 mg/kg
phosphate (PO43-): ≤5 mg/kg
sulfate (SO42-): ≤10 mg/kg

cation traces

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: ≤5 mg/kg
Pb: ≤5 mg/kg
Zn: ≤5 mg/kg

storage temp.

2-8°C

SMILES string

[H]N([H])[H].NC(O)=O

InChI

1S/CH3NO2.H3N/c2-1(3)4;/h2H2,(H,3,4);1H3

InChI key

BVCZEBOGSOYJJT-UHFFFAOYSA-N

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Other Notes

this product will be discontinued, please find the alternative product here :
101134

Pictograms

CorrosionExclamation mark
GHS05,GHS07

Signal Word

Danger

Hazard Statements

H302,H315,H318

Hazard Classifications

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

Storage Class Code

11 - Combustible Solids

WGK

WGK 1

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
BCCG4836
BCCF5201
BCCF5863
BCCC6180
BCCC3502

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Alexey P Ilyn et al.
The Journal of organic chemistry, 71(7), 2811-2819 (2006-03-25)
We present a convenient synthesis of novel heteroaryl-fused 3-oxo-1,4-thiazepine-5-carboxamides and 5-oxo-1,4-thiazepine-3-carboxamides using a modification of four-component Ugi condensation. We demonstrate the usefulness and versatility of the developed approach for the synthesis of variously substituted compounds and discuss the scope and
An-Hua Liu et al.
Angewandte Chemie (International ed. in English), 51(45), 11306-11310 (2012-10-09)
Steric bulk controls CO(2) absorption: N-substituted amino acid salts in poly(ethylene glycol) reversibly absorb CO(2) in nearly 1:1 stoichiometry. Carbamic acid is thought to be the absorbed form of CO(2); this was supported by NMR and in situ IR spectroscopy
Jana Klimentová et al.
Bioorganic & medicinal chemistry letters, 16(7), 1981-1984 (2006-02-01)
Transkarbam 12 (T12) is a novel transdermal penetration enhancer with high activity. Its polar head group is formed by carbamic acid salt that is unstable in acidic environment and releases CO(2). To find out whether this property influences its high
Michal Novotný et al.
Bioorganic & medicinal chemistry letters, 20(9), 2726-2728 (2010-04-13)
Transkarbam 12, an ammonium carbamate formed by the reaction of dodecyl 6-aminohexanoate with carbon dioxide, is a highly active, broad-spectrum, nontoxic, and nonirritant transdermal permeation enhancer. It probably acts by a dual mechanism: a part of its activity is associated
William H Schaefer
Current drug metabolism, 7(8), 873-881 (2006-12-16)
Glucuronidation is an important mechanism used by mammalian systems to clear and eliminate both endogenous and foreign chemicals. Many functional groups are susceptible to conjugation with glucuronic acid, including hydroxyls, phenols, carboxyls, activated carbons, thiols, amines, and selenium. Primary and
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