Advanced Search



L-Histidine

SIGMA/53319 - BioUltra, ≥99.5% (NT)

Synonym: (S)-2-Amino-3-(4-imidazolyl)propionic acid; NSC 137773

CAS Number: 71-00-1
Empirical Formula (Hill Notation): C6H9N3O2
Molecular Weight: 155.15
EC Number: 200-745-3
MDL Number: MFCD00064315
Linear Formula: C6H9N3O2
Product Type: Chemical

Catalog Number PKG Qty. Price Quantity
45-53319-25G 25 g
$69.50
1/EA
Add To Favorites
45-53319-100G 100 g
$232.00
1/EA
Add To Favorites

 

λ 0.1 M in H2O
anion traces chloride (Cl-): ≤100 mg/kg
  sulfate (SO42-): ≤100 mg/kg
application(s) detection
assay ≥99.5% (NT)
cation traces Al: ≤5 mg/kg
  As: ≤0.1 mg/kg
  Ba: ≤5 mg/kg
  Bi: ≤5 mg/kg
  Ca: ≤10 mg/kg
  Cd: ≤5 mg/kg
  Co: ≤5 mg/kg
  Cr: ≤5 mg/kg
  Cu: ≤5 mg/kg
  Fe: ≤5 mg/kg
  K: ≤50 mg/kg
  Li: ≤5 mg/kg
  Mg: ≤5 mg/kg
  Mn: ≤5 mg/kg
  Mo: ≤5 mg/kg
  Na: ≤50 mg/kg
  NH4+: ≤500 mg/kg
  Ni: ≤5 mg/kg
  Pb: ≤5 mg/kg
  Sr: ≤5 mg/kg
  Zn: ≤5 mg/kg
color white
form powder or crystals
ign. residue ≤0.1% (as SO4)
impurities insoluble matter, passes filter test
  ≤0.5% foreign amino acids
InChI 1S/C6H9N3O2/c7-5(6(10)11)1-4-2-8-3-9-4/h2-3,5H,1,7H2,(H,8,9)(H,10,11)/t5-/m0/s1
InChI key HNDVDQJCIGZPNO-YFKPBYRVSA-N
loss ≤0.5% loss on drying, 110 °C
mp 282 °C (dec.) (lit.)
  ~285 °C (dec.)
optical activity [α]20/D −39±1°, c = 2% in H2O
pH 7.0-8.0 (25 °C, 0.1 M in H2O)
product line BioUltra
Quality Level 200 
SMILES string N[C@@H](Cc1c[nH]cn1)C(O)=O
solubility H2O: 0.1 M at 20 °C, clear, colorless
UV absorption λ: 260 nm Amax: 0.05
  λ: 280 nm Amax: 0.05
Application: L-Histidine has been used for characterization of ZnO nanorod in an attempt to develop a technique for the ultra-low level detection of l-histidine.
Biochem/physiol Actions: L-Histidine is involved in the one-carbon unit metabolism. It is associated with protein methylation. L-Histidine is a part of hemoglobin structure and function. L-Histidine is a component of dipeptides with antioxidative property. Histidine serves as a precursor for the formation of histamine, which is associated with allergic responses. Urocanic acid, an immune response modulator in skin is also biosynthesised from histidine.
Biochem/physiol Actions: Precursor of histamine by action of histidine decarboxylase.
Other Notes: Amino acid spacing in isotachophoresis on polyacrylamide gels - a critical evaluation; Prevents circular DNA strand cleavage in a xanthine-xanthine oxidase system; Growth requirement of various microorganisms.
RIDADR NONH for all modes of transport
WGK Germany WGK 1
Flash Point(F) Not applicable
Flash Point(C) Not applicable
Purity ≥99.5% (NT)
mp 282 °C (dec.) (lit.); ~285 °C (dec.)
UNSPSC 12352209

The following items have been added to your cart:

Choose a favorite list for this item:

Catalog Number Description Price
$

Returns/Order support

Please fill out the form below if you want to request order support from Krackeler Scientific.


Quick Order

* Required


New Year Price Updates

We are currently working diligently to update our website pricing information for the New Year. If you place an order, you will be acknowledged with any corrected pricing. If you'd like the most current information sooner, please don't hesitate to drop us an email or give us a call and we'd be happy to assist. Thank you for your patience while we are updating.

800-334-7725
office@krackeler.com


Play Video

To Request a Quote

  1. Search or Browse for items and add to them to your Shopping Cart.
  2. Click the "Request Quote" button at the bottom of the Shopping Cart page.
  3. Fill out required fields.
  4. Optionally you can convert to standard checkout mode by choosing a payment type.
  5. Click "Request Quote" at the bottom of the page.

You will be contacted with a quote.

To Order From a Quote

  1. Register and login to the website.
  2. Receive a quote from your sales representative or customer service.
  3. Have your copy of the quote in hand.
  4. Visit our quote module to search for your quote.
Back to Top