| Identification | More | [Name]
Anilinoacetic acid | [CAS]
103-01-5 | [Synonyms]
AKOS B003332
ANILINOACETIC ACID
AURORA KA-3653
H-PHENYLGLY-OH
N-ALPHA-AMINOPHENYLACETIC ACID
N-PHENYLAMINOACETIC ACID
N-PHENYLGLYCIN
N-PHENYLGLYCINE
N-PHENYL-GLY-OH
(PHENYLAMINO)ACETIC ACID
PHENYL GLYCINE
PH-GLY-OH
RARECHEM AL BO 1139
Glycine, N-phenyl-
2-(phenylamino)acetic acid
Glycine, N-phenyl-(6CI,7CI,8CI,9CI)
N--Aminophenylaceticacid
N-PhenylGlocine
N-A-AMINOPHENYLACETICACID
N-alpha-Phenyl-glycine | [EINECS(EC#)]
203-070-2 | [Molecular Formula]
C8H9NO2 | [MDL Number]
MFCD00014009 | [Molecular Weight]
151.16 | [MOL File]
103-01-5.mol |
| Chemical Properties | Back Directory | [Appearance]
ochre to yellow-brown fine powder | [Melting point ]
121-123 °C (lit.) | [Boiling point ]
273.17°C (rough estimate) | [density ]
1.2023 (rough estimate) | [refractive index ]
1.5810 (estimate) | [storage temp. ]
Store at RT. | [solubility ]
DMSO (Sparingly), Methanol (Slightly) | [form ]
Fine Powder | [pka]
1.83, 4.39(at 25℃) | [color ]
Ochre to yellow-brown | [Water Solubility ]
moderately soluble | [Merck ]
14,7292 | [BRN ]
509838 | [Major Application]
peptide synthesis | [InChI]
1S/C8H9NO2/c10-8(11)6-9-7-4-2-1-3-5-7/h1-5,9H,6H2,(H,10,11) | [InChIKey]
NPKSPKHJBVJUKB-UHFFFAOYSA-N | [SMILES]
OC(=O)CNc1ccccc1 | [CAS DataBase Reference]
103-01-5(CAS DataBase Reference) | [NIST Chemistry Reference]
N-Phenylglycine(103-01-5) | [EPA Substance Registry System]
103-01-5(EPA Substance) |
| Safety Data | Back Directory | [Symbol(GHS) ]
GHS07 | [Signal word ]
Warning | [Hazard statements ]
H315-H319-H335 | [Precautionary statements ]
P261-P305+P351+P338 | [Risk Statements ]
36/37/38 | [Safety Statements ]
S22:Do not breathe dust .
S24/25:Avoid contact with skin and eyes . | [WGK Germany ]
3
| [TSCA ]
Yes | [HazardClass ]
IRRITANT | [HS Code ]
29224995 | [Storage Class]
11 - Combustible Solids |
| Hazard Information | Back Directory | [Chemical Properties]
ochre to yellow-brown fine powder | [Uses]
N-Phenylglycine is a derivative of Glycine (G615990). N-Phenylglycine is also sometimes coupled with Glycidyl methacrylate to create a surface active comonomer that promotes adhesive bonding of materials to hard tooth tissues. | [Definition]
ChEBI: A glycine carrying an N-phenyl substituent. | [reaction suitability]
reaction type: solution phase peptide synthesis |
|
| Company Name: |
J & K SCIENTIFIC LTD.
|
| Telephone: |
18210857532 18210857532 |
| Website: |
https://www.jkchemical.com |
| Company Name: |
Alfa Aesar
|
| Telephone: |
400-6106006 |
| Website: |
http://chemicals.thermofisher.cn |
| Company Name: |
Energy Chemical
|
| Telephone: |
400-0056266 |
| Website: |
www.energy-chemical.com |
|