+1 858-523-8231
Login | Register
menu
AA Blocks, Building Blocks, Catalysts, Inhibitors
Login | Register
4229-44-1,MFCD00012597
Catalog No.:AA0035BN

4229-44-1 | N-Methylhydroxylamine HCl

Pack Size
Purity
Availability
Price(USD)
Quantity
  
1g
97%
in stock  
$7.00   $5.00
- +
5g
97%
in stock  
$11.00   $8.00
- +
10g
97%
in stock  
$20.00   $14.00
- +
25g
97%
in stock  
$26.00   $19.00
- +
100g
97%
in stock  
$103.00   $72.00
- +
500g
97%
in stock  
$513.00   $359.00
- +
  • Technical Information
  • Properties
  • Upstream Synthesis Route
  • Downstream Synthesis Route
  • Literature
  • Request for Quotation
  • Download SDS
Technical Information
Catalog Number:
AA0035BN
Chemical Name:
N-Methylhydroxylamine HCl
CAS Number:
4229-44-1
Molecular Formula:
CH6ClNO
Molecular Weight:
83.5174
MDL Number:
MFCD00012597
SMILES:
CNO.Cl
NSC Number:
48213
Properties
Properties
 
Form:
Solid  
MP:
86-88 °C(lit.)  
Solubility:
H2O: 0.1 g/mL, clear, very faintly yellow  
Stability:
Hygroscopic  
Storage:
Inert atmosphere;Room Temperature;  

Computed Properties
 
Complexity:
4.8  
Covalently-Bonded Unit Count:
2  
Defined Atom Stereocenter Count:
0  
Defined Bond Stereocenter Count:
0  
Formal Charge:
0  
Heavy Atom Count:
4  
Hydrogen Bond Acceptor Count:
2  
Hydrogen Bond Donor Count:
3  
Isotope Atom Count:
0  
Rotatable Bond Count:
0  
Undefined Atom Stereocenter Count:
0  
Undefined Bond Stereocenter Count:
0  

Synonyms
 
  
Upstream Synthesis Route

[1]JournalofFluorineChemistry,1987,vol.36,p.247-272

[1]Patent:US6153793,2000,A,

[2]Patent:US6153793,2000,A,

[1]JournaloftheAmericanChemicalSociety,2013,vol.135,#31,p.11521-11524

[2]OrganicLetters,2005,vol.7,#25,p.5729-5732

[3]OrganicLetters,2007,vol.9,#20,p.4009-4012

[4]Chemical&PharmaceuticalBulletin,1982,vol.30,#4,p.1221-1224

[5]OrganicLetters,2009,vol.11,#22,p.5210-5213

[6]OrganicLetters,2017,vol.19,#6,p.1314-1317

[7]EuropeanJournalofOrganicChemistry,2017,vol.2017,#25,p.3722-3728

[8]Patent:US2013/149242,2013,A1,.Locationinpatent:Paragraph0107

[9]OrganicandBiomolecularChemistry,2017,vol.15,#7,p.1686-1699

[10]Chemistry-AEuropeanJournal,2015,vol.21,#52,p.18944-18948

[11]Patent:WO2018/5881,2018,A1,.Locationinpatent:Page/Pagecolumn343

[1]JournalofOrganicChemistry,2003,vol.68,#1,p.195-197

[1]Patent:WO2015/80936,2015,A1,.Locationinpatent:Page/Pagecolumn10

Downstream Synthesis Route

[1]Bittner,S.etal.[TetrahedronLetters,1965,p.95-99]

[1]Bittner,S.etal.[TetrahedronLetters,1965,p.95-99]

4229-44-1    583-47-1   
C10H14N2O2 

[1]TetrahedronLetters,1965,p.95-99

[1]Tetrahedron,1967,vol.23,p.4395-4407

[1]Tetrahedron,1967,vol.23,p.4395-4407

Literature

Title: Radiosynthesis and biodistribution of a prosthetic group (¹⁸F-FENMA) conjugated to cyclic RGD peptides.

Journal: Bioconjugate chemistry 20101215

Title: Tris-(hydroxyamino)triazines: high-affinity chelating tridentate O,N,O-hydroxylamine ligand for the cis-V(V)O2(+) cation.

Journal: Dalton transactions (Cambridge, England : 2003) 20101014

Title: Nitrosation of N-methylhydroxylamine by nitroprusside. A kinetic and mechanistic study.

Journal: Dalton transactions (Cambridge, England : 2003) 20081007

Title: Highly efficient three-component synthesis of beta-lactams from N-methylhydroxylamine, aldehydes, and phenylacetylene.

Journal: Chemistry, an Asian journal 20060717

Title: Substituent effects on 15N NMR chemical shifts in selected N-alkylthiohydroxamic acids. A comparative study.

Journal: Magnetic resonance in chemistry : MRC 20050101

Title: Reactivity and chemical synthesis of L-pyrrolysine- the 22(nd) genetically encoded amino acid.

Journal: Chemistry & biology 20040901

Title: Beta D305A mutant of tryptophan synthase shows strongly perturbed allosteric regulation and substrate specificity.

Journal: Biochemistry 20010626

Quotation Request
Company Name:
*
Contact Person:
*
Email:
*
Quantity Required:
*
Country:
Additional Info:
Submit
SDS
Related Products of 4229-44-1
593-77-1

593-77-1
Building Blocks
More >
Historical Records
263169-24-0

263169-24-0

 130416-46-5

130416-46-5

 174648-95-4

174648-95-4

 1856098-22-0

1856098-22-0

 1049569-35-8

1049569-35-8

 1249754-30-0

1249754-30-0
Tags:4229-44-1 Molecular Formula|4229-44-1 MDL|4229-44-1 SMILES|4229-44-1 N-Methylhydroxylamine HCl
Catalog No.: AA0035BN
4229-44-1,MFCD00012597
4229-44-1 | N-Methylhydroxylamine HCl
Pack Size： 1g
Purity： 97%
in stock
$7.00 $5.00
Pack Size： 5g
Purity： 97%
in stock
$11.00 $8.00
Pack Size： 10g
Purity： 97%
in stock
$20.00 $14.00
Pack Size： 25g
Purity： 97%
in stock
$26.00 $19.00
Pack Size： 100g
Purity： 97%
in stock
$103.00 $72.00
Pack Size： 500g
Purity： 97%
in stock
$513.00 $359.00
Quantity
- +
Add to Card
Order Now
bulk Quotation Request
Technical Information
Catalog Number: AA0035BN
Chemical Name: N-Methylhydroxylamine HCl
CAS Number: 4229-44-1
Molecular Formula: CH6ClNO
Molecular Weight: 83.5174
MDL Number: MFCD00012597
SMILES: CNO.Cl
NSC Number: 48213
Properties
Form: Solid  
MP: 86-88 °C(lit.)  
Solubility: H2O: 0.1 g/mL, clear, very faintly yellow  
Stability: Hygroscopic  
Storage: Inert atmosphere;Room Temperature;  
Complexity: 4.8  
Covalently-Bonded Unit Count: 2  
Defined Atom Stereocenter Count: 0  
Defined Bond Stereocenter Count: 0  
Formal Charge: 0  
Heavy Atom Count: 4  
Hydrogen Bond Acceptor Count: 2  
Hydrogen Bond Donor Count: 3  
Isotope Atom Count: 0  
Rotatable Bond Count: 0  
Undefined Atom Stereocenter Count: 0  
Undefined Bond Stereocenter Count: 0  
69:   
Upstream Synthesis Route
700-16-3    4229-44-1    1682-20-8 

[1]JournalofFluorineChemistry,1987,vol.36,p.247-272

7148-06-3    4229-44-1    1118-68-9    65753-93-7 

[1]Patent:US6153793,2000,A,

[2]Patent:US6153793,2000,A,

24424-99-5    4229-44-1    19689-97-5 

[1]JournaloftheAmericanChemicalSociety,2013,vol.135,#31,p.11521-11524

[2]OrganicLetters,2005,vol.7,#25,p.5729-5732

[3]OrganicLetters,2007,vol.9,#20,p.4009-4012

[4]Chemical&PharmaceuticalBulletin,1982,vol.30,#4,p.1221-1224

[5]OrganicLetters,2009,vol.11,#22,p.5210-5213

[6]OrganicLetters,2017,vol.19,#6,p.1314-1317

[7]EuropeanJournalofOrganicChemistry,2017,vol.2017,#25,p.3722-3728

[8]Patent:US2013/149242,2013,A1,.Locationinpatent:Paragraph0107

[9]OrganicandBiomolecularChemistry,2017,vol.15,#7,p.1686-1699

[10]Chemistry-AEuropeanJournal,2015,vol.21,#52,p.18944-18948

[11]Patent:WO2018/5881,2018,A1,.Locationinpatent:Page/Pagecolumn343

71872-03-2    4229-44-1    19689-97-5 

[1]JournalofOrganicChemistry,2003,vol.68,#1,p.195-197

593-77-1    4229-44-1 

[1]Patent:WO2015/80936,2015,A1,.Locationinpatent:Page/Pagecolumn10

Downstream Synthesis Route
2185-00-4    4229-44-1    802828-37-1 

[1]Bittner,S.etal.[TetrahedronLetters,1965,p.95-99]

2185-00-4    4229-44-1    120939-73-3 

[1]Bittner,S.etal.[TetrahedronLetters,1965,p.95-99]

4229-44-1    583-47-1   
C10H14N2O2 

[1]TetrahedronLetters,1965,p.95-99

4229-44-1    1619-58-5    17399-64-3 

[1]Tetrahedron,1967,vol.23,p.4395-4407

4229-44-1    1619-58-5    17415-30-4 

[1]Tetrahedron,1967,vol.23,p.4395-4407

Literature fold

Title: Radiosynthesis and biodistribution of a prosthetic group (¹⁸F-FENMA) conjugated to cyclic RGD peptides.

Journal: Bioconjugate chemistry20101215

Title: Tris-(hydroxyamino)triazines: high-affinity chelating tridentate O,N,O-hydroxylamine ligand for the cis-V(V)O2(+) cation.

Journal: Dalton transactions (Cambridge, England : 2003)20101014

Title: Nitrosation of N-methylhydroxylamine by nitroprusside. A kinetic and mechanistic study.

Journal: Dalton transactions (Cambridge, England : 2003)20081007

Title: Highly efficient three-component synthesis of beta-lactams from N-methylhydroxylamine, aldehydes, and phenylacetylene.

Journal: Chemistry, an Asian journal20060717

Title: Substituent effects on 15N NMR chemical shifts in selected N-alkylthiohydroxamic acids. A comparative study.

Journal: Magnetic resonance in chemistry : MRC20050101

Title: Reactivity and chemical synthesis of L-pyrrolysine- the 22(nd) genetically encoded amino acid.

Journal: Chemistry & biology20040901

Title: Beta D305A mutant of tryptophan synthase shows strongly perturbed allosteric regulation and substrate specificity.

Journal: Biochemistry20010626

Related Products of of 4229-44-1
593-77-1
593-77-1
Building Blocks More >
51429-74-4
51429-74-4
Phosphomolybdic Acid Hydrate
AA0035EM | MFCD00011341
38707-70-9
38707-70-9
8-Quinolinecarbaldehyde
AA0035HI | MFCD00805837
916578-53-5
916578-53-5
tert-Butyl4-(chloromethyl)phenylcarbamate
AA0035KO | MFCD14156082
75-94-5
75-94-5
Trichlorovinylsilane
AA0035NM | MFCD00000482
99611-76-4
99611-76-4
2,2′:5′,2′′-Terthiophene, homopolymer
AA01X43S | MFCD00012167
95408-45-0
95408-45-0
1,1'-Bis(di-tert-butylphosphino)ferrocene palladium dichloride
AA0035TQ | MFCD08064219
885276-93-7
885276-93-7
Ethyl 5-bromopyrazolo[1,5-a]pyridine-3-carboxylate
AA0035X1 | MFCD06739182
944401-56-3
944401-56-3
5-Bromo-4-(trifluoromethyl)pyridin-2-amine
AA00360A | MFCD09864896
142994-06-7
142994-06-7
2-(Methylsulfonyl)-4-(trifluoromethyl)benzoic acid
AA00363W | MFCD09037774
89570-85-4
89570-85-4
2-Hydrazinyl-5-trifluoromethylpyridine
AA003671 | MFCD00236724
Historical Records
263169-24-0
263169-24-0
130416-46-5
130416-46-5
174648-95-4
174648-95-4
1856098-22-0
1856098-22-0
1049569-35-8
1049569-35-8
1249754-30-0
1249754-30-0
Submit
© 2017 AA BLOCKS, INC. All rights reserved.