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2-AMINOHEPTANOIC ACID

CAS No.
1115-90-8
Chemical Name:
2-AMINOHEPTANOIC ACID
Synonyms
NSC20146;ABA,ABSCISIC ACID;2-AMINOENANTHIC ACID;2-AMINOHEPTANOIC ACID;2-azanylheptanoic acid;Heptanoic acid, 2-amino-;D,L 2-AMINOHEPTANOIC ACID;(+/-)-2-AMINOPIMELIC ACID;2-Aminoheptanoicacidpurum;2-AMINOHEPTANOIC ACID[095H]
CBNumber:
CB9250662
Molecular Formula:
C7H15NO2
Molecular Weight:
145.2
MDL Number:
MFCD00136760
MOL File:
1115-90-8.mol
MSDS File:
SDS
Last updated:2026-01-13 11:26:57
Product description Number Pack Size Price
DL-2-Aminoheptanoicacid FA149881 100mg $55
DL-2-Aminoheptanoicacid FA149881 250mg $105
DL-2-Aminoheptanoicacid FA149881 500mg $170
DL-2-Aminoheptanoic acid 95+% AS85836 1g $198
DL-2-Aminoheptanoicacid FA149881 1g $260

2-AMINOHEPTANOIC ACID Properties

Melting point ~280 °C (dec.)
Boiling point 251.0±23.0 °C(Predicted)
Density 1.017±0.06 g/cm3(Predicted)
storage temp. Sealed in dry,Room Temperature
pka 2.55±0.24(Predicted)
form powder
color white to faint beige
BRN 1722018
Major Application detection
peptide synthesis
InChI 1S/C7H15NO2/c1-2-3-4-5-6(8)7(9)10/h6H,2-5,8H2,1H3,(H,9,10)
InChIKey RDFMDVXONNIGBC-UHFFFAOYSA-N
SMILES CCCCCC(N)C(O)=O
CAS DataBase Reference 1115-90-8(CAS DataBase Reference)
UNSPSC Code 12352200
NACRES NA.22

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS07
Signal word  Warning
Hazard statements  H315-H319-H335
Precautionary statements  P261-P305+P351+P338
PPE Eyeshields, Gloves, type N95 (US)
WGK Germany  3
Storage Class 11 - Combustible Solids

2-AMINOHEPTANOIC ACID price More Price(17)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Biosynth Carbosynth FA149881 DL-2-Aminoheptanoicacid 1115-90-8 100mg $55 2021-12-16 Buy
Biosynth Carbosynth FA149881 DL-2-Aminoheptanoicacid 1115-90-8 250mg $105 2021-12-16 Buy
Biosynth Carbosynth FA149881 DL-2-Aminoheptanoicacid 1115-90-8 500mg $170 2021-12-16 Buy
Activate Scientific AS85836 DL-2-Aminoheptanoic acid 95+% 1115-90-8 1g $198 2021-12-16 Buy
Biosynth Carbosynth FA149881 DL-2-Aminoheptanoicacid 1115-90-8 1g $260 2021-12-16 Buy
Product number Packaging Price Buy
FA149881 100mg $55 Buy
FA149881 250mg $105 Buy
FA149881 500mg $170 Buy
AS85836 1g $198 Buy
FA149881 1g $260 Buy

2-AMINOHEPTANOIC ACID Chemical Properties,Uses,Production

Uses

detection
peptide synthesis

Definition

ChEBI: An alpha-amino acid that is heptanoic acid in which one of the hydrogens at position 2 is replaced by an amino group.

reaction suitability

reaction type: solution phase peptide synthesis

Synthesis

A solution of 3 g (42 mmol) of 3-buten-1-ol in 10 mL of anhydrous pyridine was cooled in an ice bath. Toluenesulfonyl chloride (7.9 g, 42 mmol) was added. After stirring for 3 hours, the mixture was poured into 30 mL of ice/concentrated HCl4/1v/v solution, extracted with 60 mL of ether and dried overnight in the refrigerator with MgSO4. The mixture was filtered, the ether was evaporated and 1.56 g (6.9 mmol) of ethyl acetamidodipropionate was dissolved in 10 mL of anhydrous THF under N2 at room temperature. Potassium tert-butoxide (0.80 g, 7 mmol) was added with vigorous stirring. The mixture was heated at 60C for 2 hours. 3-Buten-1-ol 4-methylbenzenesulfonate (1.5 g, 6.9 mmol) was added and the mixture was heated to reflux for 2 days. THF was removed, the residue was quenched with 10 mL of 1MHCl and the crude product was extracted with ethyl acetate (25 mL). The ethyl acetate solution was washed twice with 25 mL of water, dried over MgSO4, filtered and concentrated. The crude product was purified by column chromatography (eluent cyclohexane/ethyl acetate 2/1v/v). The diethyl ester obtained as described above was hydrolyzed to a dicarboxylate by heating at reflux for 4 h in 25 mL of 10 w% NaOH. The solution was neutralized with 6MHCl and the solvent was evaporated. The diacid was extracted with 25mL of methanol. After evaporation of the solvent, 20 mL of 1MHCl was added and the solution was refluxed for 3 hours. The solvent was evaporated and the product was dissolved in 10mL of methanol. Propylene oxide (5 mL) was added and the mixture was stirred overnight at room temperature. The precipitate was filtered and 2-aminoheptanoic acid was dried.

110-53-2
1115-90-8
Synthesis of 2-AMINOHEPTANOIC ACID from 1-Bromopentane

2-AMINOHEPTANOIC ACID Suppliers

Global( 98)Suppliers
Supplier Tel Email Country ProdList Advantage
Alchem Pharmtech,Inc.
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CONIER CHEM AND PHARMA LIMITED
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Zhengzhou Alfa Chemical Co.,Ltd
+8618530059196 sale04@alfachem.cn China 9545 58
Career Henan Chemica Co
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Dideu Industries Group Limited
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Labnetwork lnc.
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R&D Scientific Inc.
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Aladdin Scientific
tp@aladdinsci.com United States 57505 58
DAYANG CHEM (HANGZHOU) CO.,LTD
+86-88938639 +86-17705817739 info@dycnchem.com China 53802 58
Shanghai Hanhong Scientific Co., Ltd.
+undefined17612118332 Lucky@hanhonggroup.com China 5844 58

2-AMINOHEPTANOIC ACID Spectrum

2-AMINOENANTHIC ACID (+/-)-2-AMINOHEPTANEDIOIC ACID 2-AMinoheptanoic acid >=97.0% (NT) 2-azanylheptanoic acid DL-2-AMinoheptanoic acid DL-2-AMinoheptanoic acid 2-AMINOHEPTANOIC ACID[095H] 2-AMINOHEPTANOIC ACID(WXC11028) 2-AMINOHEPTANOIC ACID (+/-)-2-AMINOPIMELIC ACID D,L 2-AMINOHEPTANOIC ACID ABA,ABSCISIC ACID 2-Aminoheptanoicacidpurum NSC20146 Heptanoic acid, 2-amino- 2-AMINOHEPTANOIC ACID USP/EP/BP 1115-90-8 Linear Core Amino Acids Peptide Synthesis Specialty Synthesis Unnatural Amino Acid Derivatives