Cas no 951-55-3 (5-Methyl-DL-tryptophan)

5-Methyl-DL-tryptophan structure
5-Methyl-DL-tryptophan structure
Product Name:5-Methyl-DL-tryptophan
CAS No:951-55-3
MF:C12H14N2O2
MW:218.251762866974
MDL:MFCD00005652
CID:805967
PubChem ID:87572508
Update Time:2024-10-25

5-Methyl-DL-tryptophan Chemical and Physical Properties

Names and Identifiers

    • Tryptophan, 5-methyl-
    • 5-Methyl-DL-tryptophan
    • 2-amino-3-(5-methyl-1H-indol-3-yl)propanoic acid
    • H-Trp(5-Me)-OH
    • H-DL-Trp(5-Me)-OH
    • 5-Methyltryptophan
    • dl-5-Methyltryptophan
    • HUNCSWANZMJLPM-UHFFFAOYSA-N
    • 5-METHYL-TRYPTOPHAN
    • 2-amino-3-(5-methylindol-3-yl)propanoic acid
    • 5-Methyl tryptophan, dl-
    • AK167448
    • 5-Methyltryptophan #
    • PubChem20652
    • DL-Tryptophan, 5-methyl-
    • Tryptophan, 5-methyl-, DL-
    • 5-Methyltryptophan (ACI)
    • DL-Tryptophan, 5-methyl- (ZCI)
    • DL
    • Tryptophan, 5-methyl-, DL- (8CI)
    • (±)-5-Methyltryptophan
    • 2-Azaniumyl-3-(5-methyl-1H-indol-3-yl)propanoate
    • DL-5-Methyltryptophane
    • NSC 57695
    • DL-2-Amino-3-(5-Methylindolyl) Propionic acid
    • SCHEMBL41267
    • (2R)-2-azaniumyl-3-(5-methyl-1H-indol-3-yl)propanoate
    • CHEMBL569600
    • CS-D0272
    • M0452
    • CS-15061
    • NSC57695
    • 5-Methyl-DL-tryptophan (H-DL-Trp(5-Me)-OH)
    • MFCD00005652
    • DTXSID001314252
    • 951-55-3
    • Q27123483
    • SCHEMBL18029004
    • EINECS 213-453-6
    • CHEBI:52524
    • HY-33228
    • NSC-57695
    • AKOS003382639
    • M-5024
    • DB-057560
    • MDL: MFCD00005652
    • Inchi: 1S/C12H14N2O2/c1-7-2-3-11-9(4-7)8(6-14-11)5-10(13)12(15)16/h2-4,6,10,14H,5,13H2,1H3,(H,15,16)
    • InChI Key: HUNCSWANZMJLPM-UHFFFAOYSA-N
    • SMILES: O=C(C(CC1C2C(=CC=C(C)C=2)NC=1)N)O

Computed Properties

  • Exact Mass: 218.10600
  • Monoisotopic Mass: 218.105527694g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 3
  • Hydrogen Bond Acceptor Count: 3
  • Heavy Atom Count: 16
  • Rotatable Bond Count: 3
  • Complexity: 270
  • Covalently-Bonded Unit Count: 1
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 1
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • Surface Charge: 0
  • Tautomer Count: nothing
  • XLogP3: -0.7
  • Topological Polar Surface Area: 79.1

Experimental Properties

  • Color/Form: Not determined
  • Density: 1.1402 (rough estimate)
  • Melting Point: ~275?°C (dec.)
  • Boiling Point: 358.94°C (rough estimate)
  • Flash Point: 229.1±28.7 °C
  • Refractive Index: 1.6660 (estimate)
  • PSA: 79.11000
  • LogP: 2.13100
  • Solubility: Not determined
  • Vapor Pressure: 0.0±1.2 mmHg at 25°C

5-Methyl-DL-tryptophan Customs Data

  • HS CODE:2933990090
  • Customs Data:

    China Customs Code:

    2933990090

    Overview:

    2933990090. Other heterocyclic compounds containing only nitrogen heteroatoms. VAT:17.0%. Tax refund rate:13.0%. Regulatory conditions:nothing. MFN tariff:6.5%. general tariff:20.0%

    Declaration elements:

    Product Name, component content, use to, Please indicate the appearance of Urotropine, 6- caprolactam please indicate the appearance, Signing date

    Summary:

    2933990090. heterocyclic compounds with nitrogen hetero-atom(s) only. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%

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5-Methyl-DL-tryptophan Production Method

Production Method 1

Reaction Conditions
1.1 Catalysts: Sodium hydroxide Solvents: Ethanol ,  Water ;  2 h, pH 8.5, rt
1.2 Reagents: Hydrochloric acid ;  pH 1.5, rt
1.3 Reagents: Zinc Solvents: Acetic acid ;  rt → 50 °C; 4 h, 50 °C
1.4 Reagents: Hydrochloric acid Solvents: Water ;  pH 1.5
1.5 Reagents: Sodium ,  Ammonia Catalysts: Ferric nitrate Solvents: Dimethylformamide ,  Water ;  50 °C; 1 h, rt
1.6 Reagents: Sodium hydroxide Solvents: Water ;  1.5 h, pH 9.5, rt → 85 °C
1.7 Reagents: Hydrochloric acid Solvents: Water ;  pH 6, 66 °C
Reference
Amino acid derivative, feed composition and application thereof
, China, , ,

Production Method 2

Reaction Conditions
Reference
Hydrocarbon synthesis
, Japan, , ,

Production Method 3

Reaction Conditions
1.1 Reagents: Acetic anhydride Solvents: Acetic acid ;  12 h, 75 °C
1.2 Reagents: Sodium hydroxide Solvents: Water ;  rt → 60 °C; 6 h, 60 °C
1.3 Reagents: Acetic acid ;  pH 5, cooled
Reference
Synthesis method of 2-hydroxy-3-(substituted 1H-indol-3-yl)propionic acid compound from single substituted indole and DL-serine
, China, , ,

Production Method 4

Reaction Conditions
Reference
Bacterial synthesis of L-tryptophan and its analogs. I. Synthesis of L-tryptophan from pyruvate, ammonia, and indole
Nakazawa, Hidetsugu; Enei, Hitoshi; Okumura, Shinji; Yamada, Hideaki, Agricultural and Biological Chemistry, 1972, 36(13), 2523-8

5-Methyl-DL-tryptophan Raw materials

5-Methyl-DL-tryptophan Preparation Products

5-Methyl-DL-tryptophan Suppliers

Amadis Chemical Company Limited
Gold Member
Audited Supplier Audited Supplier
(CAS:951-55-3)5-Methyl-DL-tryptophan
Order Number:A845194
Stock Status:in Stock
Quantity:5g
Purity:99%
Pricing Information Last Updated:Friday, 30 August 2024 07:05
Price ($):566.0
Recommended suppliers
Amadis Chemical Company Limited
(CAS:951-55-3)5-Methyl-DL-tryptophan
A845194
Purity:99%
Quantity:5g
Price ($):566.0
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