Product Name

  • Name

    N-(4-Aminobenzoyl)-beta-alanine

  • EINECS 616-017-7
  • CAS No. 7377-08-4
  • Article Data7
  • CAS DataBase
  • Density 1.303 g/cm3
  • Solubility
  • Melting Point 152-154 °C(lit.)
  • Formula C10H12N2O3
  • Boiling Point 519.4 °C at 760 mmHg
  • Molecular Weight 208.217
  • Flash Point 267.9 °C
  • Transport Information
  • Appearance white to light orange-brown crystalline powder
  • Safety 26-37/39
  • Risk Codes 36/37/38
  • Molecular Structure Molecular Structure of 7377-08-4 (N-(4-Aminobenzoyl)-beta-alanine)
  • Hazard Symbols IrritantXi
  • Synonyms b-Alanine, N-(p-aminobenzoyl)-(6CI,7CI,8CI);3-(4-Aminobenzoylamino)propionic acid;3-[(4-Aminobenzoyl)amino]propanoic acid;p-Amino-N-benzoyl-b-alanine;
  • PSA 92.42000
  • LogP 1.44540

Synthetic route

N-(4-nitrobenzoyl)-beta-alanine
59642-21-6

N-(4-nitrobenzoyl)-beta-alanine

N-(4-aminobenzoyl)-B-alanine
7377-08-4

N-(4-aminobenzoyl)-B-alanine

Conditions
ConditionsYield
With 1% Pd/C; hydrogen In methanol at 20℃;98%
With palladium 10% on activated carbon; hydrogen In methanol at 20℃; under 750.075 Torr; for 3h; Inert atmosphere;89%
With palladium on activated carbon; hydrogen In methanol at 20℃; under 750.075 Torr; for 3h;75%
4-nitro-benzoyl chloride
122-04-3

4-nitro-benzoyl chloride

N-(4-aminobenzoyl)-B-alanine
7377-08-4

N-(4-aminobenzoyl)-B-alanine

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: aq. NaOH solution
2: zinc; acid
View Scheme
Multi-step reaction with 2 steps
1: sodium hydroxide / 2.5 h / 0 - 20 °C
2: hydrogen; palladium 10% on activated carbon / methanol / 3 h / 20 °C / 750.08 Torr / Inert atmosphere
View Scheme
Multi-step reaction with 3 steps
1: sodium hydroxide / water / 3 h / 5 °C
2: hydrogen / water / 20 °C / 760.05 Torr
3: hydrogenchloride / water / 0.17 h / pH 1 - 2
View Scheme
Multi-step reaction with 2 steps
1: sodium hydroxide / 0.5 h / 0 °C
2: palladium on activated carbon; hydrogen / methanol / 3 h / 20 °C / 750.08 Torr
View Scheme
Na(1+)*C10H9N2O5(1-)

Na(1+)*C10H9N2O5(1-)

N-(4-aminobenzoyl)-B-alanine
7377-08-4

N-(4-aminobenzoyl)-B-alanine

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: hydrogen / water / 20 °C / 760.05 Torr
2: hydrogenchloride / water / 0.17 h / pH 1 - 2
View Scheme
Na(1+)*C10H11N2O3(1-)

Na(1+)*C10H11N2O3(1-)

N-(4-aminobenzoyl)-B-alanine
7377-08-4

N-(4-aminobenzoyl)-B-alanine

Conditions
ConditionsYield
With hydrogenchloride In water for 0.166667h; pH=1 - 2;
N-(4-aminobenzoyl)-B-alanine
7377-08-4

N-(4-aminobenzoyl)-B-alanine

phenol
108-95-2

phenol

(E)-3-(4-((4-hydroxyphenyl)diazenyl)benzamido)propanoic acid

(E)-3-(4-((4-hydroxyphenyl)diazenyl)benzamido)propanoic acid

Conditions
ConditionsYield
Stage #1: N-(4-aminobenzoyl)-B-alanine With hydrogenchloride; sodium nitrite In water at 0℃; for 1h;
Stage #2: phenol With sodium carbonate; sodium hydroxide In water at 0℃; pH=8;
97%
N-(4-aminobenzoyl)-B-alanine
7377-08-4

N-(4-aminobenzoyl)-B-alanine

salicylic acid
69-72-7

salicylic acid

balsalazide

balsalazide

Conditions
ConditionsYield
Stage #1: N-(4-aminobenzoyl)-B-alanine With hydrogenchloride; sodium nitrite In water at 0 - 5℃; for 1h;
Stage #2: salicylic acid With sodium carbonate; sodium hydroxide In water at 0 - 5℃; for 1h;
95%
Stage #1: N-(4-aminobenzoyl)-B-alanine With methanesulfonic acid; sodium nitrite In water at 10 - 12℃; for 0.5h;
Stage #2: salicylic acid With sodium hydroxide; sodium carbonate In water at 7 - 12℃; for 3h;
Stage #3: With hydrogenchloride; water at 60 - 65℃; for 3h; pH=4.0 - 4.5; Product distribution / selectivity;
90%
Stage #1: N-(4-aminobenzoyl)-B-alanine With hydrogenchloride; sodium nitrite In water at 0℃; for 1h;
Stage #2: salicylic acid With sodium carbonate; sodium hydroxide In water at 0℃; pH=8;
85%
Stage #1: N-(4-aminobenzoyl)-B-alanine With sodium nitrite In water at -5 - 0℃; for 1.5h;
Stage #2: salicylic acid With sodium carbonate; sodium hydroxide In water at -5 - 0℃; for 3h; pH=7.5 - 8.5;
N-(4-aminobenzoyl)-B-alanine
7377-08-4

N-(4-aminobenzoyl)-B-alanine

ethanol
64-17-5

ethanol

C12H16N2O3*ClH

C12H16N2O3*ClH

Conditions
ConditionsYield
With thionyl chloride at 0℃; for 5h; Inert atmosphere; Reflux;93%
N-(4-aminobenzoyl)-B-alanine
7377-08-4

N-(4-aminobenzoyl)-B-alanine

4-hydroxy-benzoic acid
99-96-7

4-hydroxy-benzoic acid

3-[4-(4-hydroxy-phenyl-azo)-benzoyl-amino]propionic acid

3-[4-(4-hydroxy-phenyl-azo)-benzoyl-amino]propionic acid

Conditions
ConditionsYield
Stage #1: N-(4-aminobenzoyl)-B-alanine With hydrogenchloride In water at 20 - 25℃;
Stage #2: With sodium nitrite In water at -2 - 2℃;
Stage #3: 4-hydroxy-benzoic acid Further stages;
91%
N-(4-aminobenzoyl)-B-alanine
7377-08-4

N-(4-aminobenzoyl)-B-alanine

acetic anhydride
108-24-7

acetic anhydride

3-(4-acetylamino-benzoylamino)propionic acid
212198-64-6

3-(4-acetylamino-benzoylamino)propionic acid

Conditions
ConditionsYield
With acetic acid In water at 30 - 45℃;90%
N-(4-aminobenzoyl)-B-alanine
7377-08-4

N-(4-aminobenzoyl)-B-alanine

β-(N,N-diethylamino)propiophenone hydrochloride
884-12-8

β-(N,N-diethylamino)propiophenone hydrochloride

3-[4-(3-oxo-3-phenylpropylamino)benzamido]-propanoic acid

3-[4-(3-oxo-3-phenylpropylamino)benzamido]-propanoic acid

Conditions
ConditionsYield
In water Heating;87%
N-(4-aminobenzoyl)-B-alanine
7377-08-4

N-(4-aminobenzoyl)-B-alanine

8-formyl-4-methyl-7-hydroxycoumarin
14003-96-4

8-formyl-4-methyl-7-hydroxycoumarin

7-hydroxy-4-methyl-8-(4'-(N-carboxyethylformamido)phenylimino)methyl-2H-1-benzopyran-2-one

7-hydroxy-4-methyl-8-(4'-(N-carboxyethylformamido)phenylimino)methyl-2H-1-benzopyran-2-one

Conditions
ConditionsYield
In ethanol Reflux;85.1%
N-(4-aminobenzoyl)-B-alanine
7377-08-4

N-(4-aminobenzoyl)-B-alanine

A

3-(4-hydroxybenzamido)propanoic acid
773838-08-7

3-(4-hydroxybenzamido)propanoic acid

B

4-((2-carboxyethyl)carbamoyl)benzenediazonium chloride

4-((2-carboxyethyl)carbamoyl)benzenediazonium chloride

Conditions
ConditionsYield
With hydrogenchloride; nitric acid; sodium nitrite In water at 20℃; for 1h; Reagent/catalyst;A 7%
B 84%
N-(4-aminobenzoyl)-B-alanine
7377-08-4

N-(4-aminobenzoyl)-B-alanine

A

3-(4-hydroxybenzamido)propanoic acid
773838-08-7

3-(4-hydroxybenzamido)propanoic acid

B

4-((2-carboxyethyl)carbamoyl)benzenediazonium chloride

4-((2-carboxyethyl)carbamoyl)benzenediazonium chloride

C

3-[(4-chlorobenzoyl)amino]propionic acid
440341-75-3

3-[(4-chlorobenzoyl)amino]propionic acid

Conditions
ConditionsYield
With hydrogenchloride; nitric acid; sodium nitrite In water at 20℃; for 1h; Reagent/catalyst;A 10%
B 80%
C 3%
N-(4-aminobenzoyl)-B-alanine
7377-08-4

N-(4-aminobenzoyl)-B-alanine

1-(4-ethoxy-phenyl)-3-diethylamino-propan-1-one; hydrochloride
101356-82-5

1-(4-ethoxy-phenyl)-3-diethylamino-propan-1-one; hydrochloride

3-{4-[3-(4-ethoxyphenyl)-3-oxopropylamino]-benzamido}propanoic acid

3-{4-[3-(4-ethoxyphenyl)-3-oxopropylamino]-benzamido}propanoic acid

Conditions
ConditionsYield
In water Heating;79%
N-(4-aminobenzoyl)-B-alanine
7377-08-4

N-(4-aminobenzoyl)-B-alanine

3-Chloropivaloyl chloride
4300-97-4

3-Chloropivaloyl chloride

3-[4-(3-Chloro-2,2-dimethyl-propionylamino)-benzoylamino]-propionic acid

3-[4-(3-Chloro-2,2-dimethyl-propionylamino)-benzoylamino]-propionic acid

Conditions
ConditionsYield
With pyridine In 1,4-dioxane for 1h; Heating;70%
N-(4-aminobenzoyl)-B-alanine
7377-08-4

N-(4-aminobenzoyl)-B-alanine

3-Diethylamino-1-(4-isopropoxy-phenyl)-propan-1-one; hydrochloride

3-Diethylamino-1-(4-isopropoxy-phenyl)-propan-1-one; hydrochloride

3-{4-[3-oxo-3-(4-propan-2-yloxyphenyl)propylamino]-benzamido}propanoic acid

3-{4-[3-oxo-3-(4-propan-2-yloxyphenyl)propylamino]-benzamido}propanoic acid

Conditions
ConditionsYield
In water Heating;68%
N-(4-aminobenzoyl)-B-alanine
7377-08-4

N-(4-aminobenzoyl)-B-alanine

4-hydroxy-benzoic acid
99-96-7

4-hydroxy-benzoic acid

2,4-bis[[4[[(2-carboxyethyl)amino]carbonyl]phenyl]azo]-3-[4-[[(2-carboxyethyl)amino]carbonyl]phenyl]phenol

2,4-bis[[4[[(2-carboxyethyl)amino]carbonyl]phenyl]azo]-3-[4-[[(2-carboxyethyl)amino]carbonyl]phenyl]phenol

Conditions
ConditionsYield
Stage #1: N-(4-aminobenzoyl)-B-alanine With hydrogenchloride In water at 20 - 25℃;
Stage #2: With sodium nitrite In water at -2 - 2℃;
Stage #3: 4-hydroxy-benzoic acid Further stages;
36%
N-(4-aminobenzoyl)-B-alanine
7377-08-4

N-(4-aminobenzoyl)-B-alanine

β-(N,N-diethylamino)-p-chloropropiophenone hyrdochloride
5409-52-9

β-(N,N-diethylamino)-p-chloropropiophenone hyrdochloride

3-{4-[3-(4-chlorophenyl)-3-oxopropylamino]-benzamido}propanoic acid

3-{4-[3-(4-chlorophenyl)-3-oxopropylamino]-benzamido}propanoic acid

Conditions
ConditionsYield
In water Heating;36%
N-(4-aminobenzoyl)-B-alanine
7377-08-4

N-(4-aminobenzoyl)-B-alanine

salicylic acid
69-72-7

salicylic acid

3-[[4-[[(2-carboxyethyl)amino]carbonyl]phenyl]azo]-2-hydroxybenzoic acid

3-[[4-[[(2-carboxyethyl)amino]carbonyl]phenyl]azo]-2-hydroxybenzoic acid

Conditions
ConditionsYield
Stage #1: N-(4-aminobenzoyl)-B-alanine With hydrogenchloride In water at 20 - 25℃;
Stage #2: With sodium nitrite In water at 0 - 2℃;
Stage #3: salicylic acid Further stages;
7%
N-(4-aminobenzoyl)-B-alanine
7377-08-4

N-(4-aminobenzoyl)-B-alanine

2,5,6-triamino-3,4-dihydro-4-pyrimidinone
1004-75-7

2,5,6-triamino-3,4-dihydro-4-pyrimidinone

2,3-dibromopropanal
5221-17-0

2,3-dibromopropanal

N-pteroyl-β-alanine
15677-93-7

N-pteroyl-β-alanine

Conditions
ConditionsYield
With sodium dichromate
With iodine
N-(4-aminobenzoyl)-B-alanine
7377-08-4

N-(4-aminobenzoyl)-B-alanine

3-(hydroxymethyl)benzo[d]oxazol-2(3H)-one
17832-99-4

3-(hydroxymethyl)benzo[d]oxazol-2(3H)-one

N-{4-[(2-oxo-benzooxazol-3-ylmethyl)-amino]-benzoyl}-β-alanine
67726-28-7

N-{4-[(2-oxo-benzooxazol-3-ylmethyl)-amino]-benzoyl}-β-alanine

Conditions
ConditionsYield
In ethanol Heating;
N-(4-aminobenzoyl)-B-alanine
7377-08-4

N-(4-aminobenzoyl)-B-alanine

3-(Hydroxymethyl)-2-benzoxazolinethione
3161-58-8

3-(Hydroxymethyl)-2-benzoxazolinethione

N-{4-[(2-thioxo-benzooxazol-3-ylmethyl)-amino]-benzoyl}-β-alanine
67726-31-2

N-{4-[(2-thioxo-benzooxazol-3-ylmethyl)-amino]-benzoyl}-β-alanine

Conditions
ConditionsYield
In ethanol Heating;
N-(4-aminobenzoyl)-B-alanine
7377-08-4

N-(4-aminobenzoyl)-B-alanine

3-hydroxymethyl-3H-benzothiazole-2-thione
3161-57-7

3-hydroxymethyl-3H-benzothiazole-2-thione

N-{4-[(2-thioxo-benzothiazol-3-ylmethyl)-amino]-benzoyl}-β-alanine
67726-34-5

N-{4-[(2-thioxo-benzothiazol-3-ylmethyl)-amino]-benzoyl}-β-alanine

Conditions
ConditionsYield
In ethanol Heating;
2,5-bis-[4-(5-oxo-2-trifluoromethyl-4,5-dihydro-oxazol-4-yl)-phenoxymethyl]-benzoyl chloride

2,5-bis-[4-(5-oxo-2-trifluoromethyl-4,5-dihydro-oxazol-4-yl)-phenoxymethyl]-benzoyl chloride

N-(4-aminobenzoyl)-B-alanine
7377-08-4

N-(4-aminobenzoyl)-B-alanine

3-(4-{2,5-bis-[4-(5-oxo-2-trifluoromethyl-4,5-dihydro-oxazol-4-yl)-phenoxymethyl]-benzoylamino}-benzoylamino)-propionic acid

3-(4-{2,5-bis-[4-(5-oxo-2-trifluoromethyl-4,5-dihydro-oxazol-4-yl)-phenoxymethyl]-benzoylamino}-benzoylamino)-propionic acid

Conditions
ConditionsYield
In dichloromethane at 4℃;
N-(4-aminobenzoyl)-B-alanine
7377-08-4

N-(4-aminobenzoyl)-B-alanine

dimethyl acetylenedicarboxylate
762-42-5

dimethyl acetylenedicarboxylate

C16H18N2O7

C16H18N2O7

Conditions
ConditionsYield
at 5 - 20℃;
N-(4-aminobenzoyl)-B-alanine
7377-08-4

N-(4-aminobenzoyl)-B-alanine

C16H16N2O6

C16H16N2O6

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: 5 - 20 °C
2: 75 percent / Eaton's reagent / 50 °C
View Scheme
N-(4-aminobenzoyl)-B-alanine
7377-08-4

N-(4-aminobenzoyl)-B-alanine

3-[4-(3,3-Dimethyl-2-oxo-azetidin-1-yl)-benzoylamino]-propionic acid

3-[4-(3,3-Dimethyl-2-oxo-azetidin-1-yl)-benzoylamino]-propionic acid

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: 70 percent / pyridine / dioxane / 1 h / Heating
2: 87 percent / sodium carbonate / dimethylformamide / 1 h / 160 °C
View Scheme
5-methylpyrazine-2-carbonyl chloride
50886-34-5

5-methylpyrazine-2-carbonyl chloride

N-(4-aminobenzoyl)-B-alanine
7377-08-4

N-(4-aminobenzoyl)-B-alanine

(2R,4'R,8a'R)-1-[(9H-fluoren-9-ylmethoxy)carbonyl]-6'-oxotetrahydro-2'H-spiro[pyrrolidine-2,7'-pyrrole[2,1-b][1,3]thiazine]-4'-carboxylic acid
894786-97-1

(2R,4'R,8a'R)-1-[(9H-fluoren-9-ylmethoxy)carbonyl]-6'-oxotetrahydro-2'H-spiro[pyrrolidine-2,7'-pyrrole[2,1-b][1,3]thiazine]-4'-carboxylic acid

C27H31N7O5S
894787-31-6

C27H31N7O5S

Conditions
ConditionsYield
Multistep reaction.;5.5 mg
naphthalen-1-yl-acetyl chloride
5121-00-6

naphthalen-1-yl-acetyl chloride

N-(4-aminobenzoyl)-B-alanine
7377-08-4

N-(4-aminobenzoyl)-B-alanine

{(5S)-1-[(9H-fluoren-9-yl-methoxy)carbonyl]-6-oxo-1,7-diazaspiro[4,5]dec-7-yl}acetic acid
894786-80-2

{(5S)-1-[(9H-fluoren-9-yl-methoxy)carbonyl]-6-oxo-1,7-diazaspiro[4,5]dec-7-yl}acetic acid

N-{3-[(5R)-7-(2-amino-2-oxoethyl)-6-oxo-1,7-diazaspiro[4,5]dec-1-yl]-3-oxopropyl}-4-[(1-naphthylacetyl)amino]benzamide
894787-21-4

N-{3-[(5R)-7-(2-amino-2-oxoethyl)-6-oxo-1,7-diazaspiro[4,5]dec-1-yl]-3-oxopropyl}-4-[(1-naphthylacetyl)amino]benzamide

Conditions
ConditionsYield
Multistep reaction.;3.5 mg
N-(4-aminobenzoyl)-B-alanine
7377-08-4

N-(4-aminobenzoyl)-B-alanine

Reaxys ID: 19845716

Reaxys ID: 19845716

Reaxys ID: 19845715

Reaxys ID: 19845715

N-(4-aminobenzoyl)-B-alanine
7377-08-4

N-(4-aminobenzoyl)-B-alanine

1-adamantyl isocyanate
4411-25-0

1-adamantyl isocyanate

C21H27N3O4

C21H27N3O4

Conditions
ConditionsYield
In N,N-dimethyl-formamide at 60 - 80℃; for 12h;
N-(4-aminobenzoyl)-B-alanine
7377-08-4

N-(4-aminobenzoyl)-B-alanine

salicylic acid
69-72-7

salicylic acid

5-[2-[4',5-bis[(2-carboxyethyl)carbamoyl]biphenyl-2-yl]diazenyl]-2-hydroxybenzoic acid

5-[2-[4',5-bis[(2-carboxyethyl)carbamoyl]biphenyl-2-yl]diazenyl]-2-hydroxybenzoic acid

Conditions
ConditionsYield
Stage #1: N-(4-aminobenzoyl)-B-alanine With hydrogenchloride In water at 20 - 25℃;
Stage #2: With sodium nitrite In water at -2 - 2℃;
Stage #3: salicylic acid Further stages;

N-(4-Aminobenzoyl)-beta-alanine Chemical Properties

Empirical Formula: C10H12N2O3
Molecular Weight: 208.2139 g/mol
Index of Refraction: 1.604
Density: 1.303 g/cm3
Flash Point: 267.9 °C
Enthalpy of Vaporization: 83.4 kJ/mol
Boiling Point: 519.4 °C at 760 mmHg
Vapour Pressure: 1.29E-11 mmHg at 25 °C
Melting point: 152-154 °C(lit.)
Appearance: White to light orange-brown crystalline powder
Structure of N-(4-Aminobenzoyl)-beta-alanine (CAS NO.7377-08-4):
                       
Product Category of N-(4-Aminobenzoyl)-beta-alanine (CAS NO.7377-08-4): Balsalazide

N-(4-Aminobenzoyl)-beta-alanine Toxicity Data With Reference

 N-(4-Aminobenzoyl)-beta-alanine (CAS NO.7377-08-4) hasn't been listed as a carcinogen by NTP, IARC, ACGIH, or CA Prop 65.

N-(4-Aminobenzoyl)-beta-alanine Safety Profile

Hazard Codes: IrritantXi
Risk Statements: 36/37/38 
R36/37/38:Irritating to eyes, respiratory system and skin.
Safety Statements: 26-37/39 
S26: In case of contact with eyes, rinse immediately with plenty of water and seek medical advice. 
S37/39:Wear suitable gloves and eye/face protection.

N-(4-Aminobenzoyl)-beta-alanine Specification

 N-(4-Aminobenzoyl)-beta-alanine , its cas register number is 7377-08-4. It also can be called 3-(4-Amino-benzoylamino)-propionic acid ; and beta-Alanine, N-(4-aminobenzoyl)- . It is hazardous, so the first aid measures and others should be known. Such as: When on the skin: first, should flush skin with plenty of water immediately for at least 15 minutes while removing contaminated clothing. Secondly, get medical aid. Or in the eyes: Flush eyes with plenty of water for at least 15 minutes, occasionally lifting the upper and lower eyelids. Then get medical aid soon. While, it's inhaled: Remove from exposure and move to fresh air immediately. Give artificial respiration while not breathing. When breathing is difficult, give oxygen. And as soon as to get medical aid. Then you have the ingesting of the product: If victim is conscious and alert, give 2-4 cupfuls of milk or water. Get medical aid immediately.
In addition, N-(4-Aminobenzoyl)-beta-alanine (CAS NO.7377-08-4) could be stable under normal temperatures and pressures, and you must not take it with strong oxidants. And also prevent it to broken down into hazardous decomposition products: irritating and toxic fumes and gases.

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